메뉴 건너뛰기




Volumn , Issue , 2012, Pages 191-293

The chemistry of marine sponges

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84943645370     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-90-481-3834-0_4     Document Type: Chapter
Times cited : (19)

References (457)
  • 1
    • 22644432311 scopus 로고    scopus 로고
    • Drugs from the sea-opportunities and obstacles
    • Proksch P, Edrada-Ebel RA, Ebel R (2003) Drugs from the sea-opportunities and obstacles. Mar Drugs 1: 5-17
    • (2003) Mar Drugs , vol.1 , pp. 5-17
    • Proksch, P.1    Edrada-Ebel, R.A.2    Ebel, R.3
  • 3
    • 66049129630 scopus 로고    scopus 로고
    • Marine sponges: Potential sources of new antimicrobial drugs
    • Laport MS, Santos OCS, Muricy G (2009) Marine sponges: potential sources of new antimicrobial drugs. Curr Pharm Biotech 10: 86-105
    • (2009) Curr Pharm Biotech , vol.10 , pp. 86-105
    • Laport, M.S.1    Santos, O.C.S.2    Muricy, G.3
  • 6
    • 0036314931 scopus 로고    scopus 로고
    • Drugs from the seas-current status and microbiological implications
    • Proksch P, Edrada RA, Ebel R (2002) Drugs from the seas-current status and microbiological implications. Appl Microbiol Biotechnol 59: 125-134
    • (2002) Appl Microbiol Biotechnol , vol.59 , pp. 125-134
    • Proksch, P.1    Edrada, R.A.2    Ebel, R.3
  • 7
    • 61449113023 scopus 로고    scopus 로고
    • Metabolites from symbiotic bacteria
    • Piel J (2009) Metabolites from symbiotic bacteria. Nat Prod Rep 26: 338-362
    • (2009) Nat Prod Rep , vol.26 , pp. 338-362
    • Piel, J.1
  • 9
    • 85008014440 scopus 로고
    • Identification of okadaic acid as a toxic component of a marine dinoflagellate Prorocentrum lima
    • Murakami Y, Oshima Y, Yasumoto T (1982) Identification of okadaic acid as a toxic component of a marine dinoflagellate Prorocentrum lima. Bull Jap Soc Fish Sci 48: 69-72
    • (1982) Bull Jap Soc Fish Sci , vol.48 , pp. 69-72
    • Murakami, Y.1    Oshima, Y.2    Yasumoto, T.3
  • 10
    • 0022453514 scopus 로고
    • Manzamine A, a novel antitumor alkaloid from a sponge
    • Sakai R, Higa T (1986) Manzamine A, a novel antitumor alkaloid from a sponge. J Am Chem Soc 108: 6404-6405
    • (1986) J Am Chem Soc , vol.108 , pp. 6404-6405
    • Sakai, R.1    Higa, T.2
  • 11
    • 0032482288 scopus 로고    scopus 로고
    • Manzamine alkaloids, syntheses and synthetic approaches
    • Magnier E, Langlois Y (1998) Manzamine alkaloids, syntheses and synthetic approaches. Tetrahedron 54: 6201-6258
    • (1998) Tetrahedron , vol.54 , pp. 6201-6258
    • Magnier, E.1    Langlois, Y.2
  • 12
    • 0000602866 scopus 로고    scopus 로고
    • Structures and biogenesis of manzamines and related alkaloids
    • Tsuda M, Kobayashi J (1997) Structures and biogenesis of manzamines and related alkaloids. Heterocycles 46: 765-794
    • (1997) Heterocycles , vol.46 , pp. 765-794
    • Tsuda, M.1    Kobayashi, J.2
  • 14
    • 45749120701 scopus 로고    scopus 로고
    • Neuritogenic activity-guided isolation of a free base form manzamine A from a marine sponge, Acanthostrongylophora af. ingens (Thiele, 1899)
    • Zhang B, Higuchi R, Miyamoto T, van Soest RWM (2008) Neuritogenic activity-guided isolation of a free base form manzamine A from a marine sponge, Acanthostrongylophora af. ingens (Thiele, 1899). Chem Pharm Bull 56: 866-869
    • (2008) Chem Pharm Bull , vol.56 , pp. 866-869
    • Zhang, B.1    Higuchi, R.2    Miyamoto, T.3    van Soest, R.W.M.4
  • 16
    • 0001104083 scopus 로고
    • Ircinals A and B from the Okinawan marine sponge Ircinia sp.: Plausible biogenetic precursors of manzamine alkaloids
    • Kondo K, Shigemori H, Kikuchi Y, Ishibashi M, Sasaki T, Kobayashi J (1992) Ircinals A and B from the Okinawan marine sponge Ircinia sp.: plausible biogenetic precursors of manzamine alkaloids. J Org Chem 57: 2480-2483
    • (1992) J Org Chem , vol.57 , pp. 2480-2483
    • Kondo, K.1    Shigemori, H.2    Kikuchi, Y.3    Ishibashi, M.4    Sasaki, T.5    Kobayashi, J.6
  • 17
    • 0028361008 scopus 로고
    • Ircinols A and B, first antipodes of manzaminerelated alkaloids from an Okinawan marine sponge
    • Tsuda M, Kawasaki N, Kobayashi J (1994) Ircinols A and B, first antipodes of manzaminerelated alkaloids from an Okinawan marine sponge. Tetrahedron 50: 7957-7960
    • (1994) Tetrahedron , vol.50 , pp. 7957-7960
    • Tsuda, M.1    Kawasaki, N.2    Kobayashi, J.3
  • 18
    • 0028277595 scopus 로고
    • Keramaphidin B, a novel pentacyclic alkaloid from a marine sponge Amphimedon sp.: A plausible biogenetic precursors of manzamine alkaloids
    • Kobayashi J, Tsuda M, Kawasaki N, Matsumoto K, Adachi T (1994) Keramaphidin B, a novel pentacyclic alkaloid from a marine sponge Amphimedon sp.: a plausible biogenetic precursors of manzamine alkaloids. Tetrahedron Lett 35: 4383-4386
    • (1994) Tetrahedron Lett , vol.35 , pp. 4383-4386
    • Kobayashi, J.1    Tsuda, M.2    Kawasaki, N.3    Matsumoto, K.4    Adachi, T.5
  • 19
    • 0030057721 scopus 로고    scopus 로고
    • Chiral resolution of (-)-keramaphidin B and isolation of manzamine L, a new b-carboline alkaloid from a sponge Amphimedon sp
    • Tsuda M, Inaba K, Kawasaki N, Honma K, Kobayashi J (1996) Chiral resolution of (-)-keramaphidin B and isolation of manzamine L, a new b-carboline alkaloid from a sponge Amphimedon sp. Tetrahedron 52: 2319-2324
    • (1996) Tetrahedron , vol.52 , pp. 2319-2324
    • Tsuda, M.1    Inaba, K.2    Kawasaki, N.3    Honma, K.4    Kobayashi, J.5
  • 20
    • 0029906190 scopus 로고    scopus 로고
    • Four new bioactive manzamine-type alkaloids from the Philippine marine sponge Xestospongia ashmorica
    • Edrada RA, Proksch P, Wray V, Witte L, Mueller WEG, van Soest RWM (1996) Four new bioactive manzamine-type alkaloids from the Philippine marine sponge Xestospongia ashmorica. J Nat Prod 59: 1056-1060
    • (1996) J Nat Prod , vol.59 , pp. 1056-1060
    • Edrada, R.A.1    Proksch, P.2    Wray, V.3    Witte, L.4    Mueller, W.E.G.5    van Soest, R.W.M.6
  • 24
    • 0033518577 scopus 로고    scopus 로고
    • Enantioselective total syntheses of ircinal A and related manzamine alkaloids
    • Martin SF, Humphrey JM, Ali A, Hillier MC (1999) Enantioselective total syntheses of ircinal A and related manzamine alkaloids. J Am Chem Soc 121: 866-867
    • (1999) J Am Chem Soc , vol.121 , pp. 866-867
    • Martin, S.F.1    Humphrey, J.M.2    Ali, A.3    Hillier, M.C.4
  • 28
    • 0001375973 scopus 로고    scopus 로고
    • Nakadomarin A, a novel hexacyclic manzamine-related alkaloid from Amphimedon sponge
    • Kobayashi J, Watanabe D, Kawasaki N, TsudaM (1997) Nakadomarin A, a novel hexacyclic manzamine-related alkaloid from Amphimedon sponge. J Org Chem 62: 9236-9239
    • (1997) J Org Chem , vol.62 , pp. 9236-9239
    • Kobayashi, J.1    Watanabe, D.2    Kawasaki, N.3    Tsuda, M.4
  • 29
    • 0032485305 scopus 로고    scopus 로고
    • Ma’eganedin A, a new manzamine alkaloid from Amphimedon sponge
    • Tsuda M, Watanabe D, Kobayashi J (1998) Ma’eganedin A, a new manzamine alkaloid from Amphimedon sponge. Tetrahedron Lett 39: 1207-1210
    • (1998) Tetrahedron Lett , vol.39 , pp. 1207-1210
    • Tsuda, M.1    Watanabe, D.2    Kobayashi, J.3
  • 31
    • 59649128696 scopus 로고    scopus 로고
    • Zamamidines A and B, new manzamine alkaloids from the sponge Amphimedon sp
    • Takahashi Y, Kubota T, Fromont J, Kobayashi J (2009) Zamamidines A and B, new manzamine alkaloids from the sponge Amphimedon sp. Org Lett 11: 21-24
    • (2009) Org Lett , vol.11 , pp. 21-24
    • Takahashi, Y.1    Kubota, T.2    Fromont, J.3    Kobayashi, J.4
  • 32
    • 59949095679 scopus 로고    scopus 로고
    • Zamamidine C, 3,4-dihydro-6-hydroxy-10,11-epoxymanzamine A, and 3,4-dihydromanzamine J N-oxide, new manzamine alkaloids from sponge Amphimedon sp
    • Yamada M, Takahashi Y, Kubota T, Fromont J, Ishiyama A, Otoguro K, Yamada H, Omura S, Kobayashi J (2009) Zamamidine C, 3,4-dihydro-6-hydroxy-10,11-epoxymanzamine A, and 3,4-dihydromanzamine J N-oxide, new manzamine alkaloids from sponge Amphimedon sp. Tetrahedron 65: 2313-2317
    • (2009) Tetrahedron , vol.65 , pp. 2313-2317
    • Yamada, M.1    Takahashi, Y.2    Kubota, T.3    Fromont, J.4    Ishiyama, A.5    Otoguro, K.6    Yamada, H.7    Omura, S.8    Kobayashi, J.9
  • 33
    • 4344668984 scopus 로고    scopus 로고
    • New manzamine alkaloids from a common Indonesian sponge and their activity against infectious and tropical parasitic diseases
    • Rao KV, Kasanah N, Wahyuono S, Tekwani BL, Schinazi RF, Hamann MT (2004) New manzamine alkaloids from a common Indonesian sponge and their activity against infectious and tropical parasitic diseases. J Nat Prod 67: 1314-1318
    • (2004) J Nat Prod , vol.67 , pp. 1314-1318
    • Rao, K.V.1    Kasanah, N.2    Wahyuono, S.3    Tekwani, B.L.4    Schinazi, R.F.5    Hamann, M.T.6
  • 34
    • 0038203630 scopus 로고    scopus 로고
    • New manzamine alkaloids with activity against infectious tropical parasitic diseases from an Indonesian sponge
    • Rao KC, Santarsiero BD, Mesecar AD, Schinazi RF, Tekwani BL, Hamann MT (2003) New manzamine alkaloids with activity against infectious tropical parasitic diseases from an Indonesian sponge. J Nat Prod 66: 823-828
    • (2003) J Nat Prod , vol.66 , pp. 823-828
    • Rao, K.C.1    Santarsiero, B.D.2    Mesecar, A.D.3    Schinazi, R.F.4    Tekwani, B.L.5    Hamann, M.T.6
  • 35
    • 33947599966 scopus 로고    scopus 로고
    • The manzamines as an example of the unique structural classes available for the discovery and optimization of infectious disease controls based on marine natural products
    • Hamann MT (2007) The manzamines as an example of the unique structural classes available for the discovery and optimization of infectious disease controls based on marine natural products. Curr Pharm Design 13: 653-660
    • (2007) Curr Pharm Design , vol.13 , pp. 653-660
    • Hamann, M.T.1
  • 39
    • 0032760487 scopus 로고    scopus 로고
    • Chemical defense of the Caribbean reef sponge Axinella corrugata against predatory fishes
    • Wilson DM, Puyama M, Fenical W, Pawlik JR (1999) Chemical defense of the Caribbean reef sponge Axinella corrugata against predatory fishes. J Chem Ecol 25: 2811-2823
    • (1999) J Chem Ecol , vol.25 , pp. 2811-2823
    • Wilson, D.M.1    Puyama, M.2    Fenical, W.3    Pawlik, J.R.4
  • 40
    • 0033917903 scopus 로고    scopus 로고
    • Structure-activity relationship of inhibition of fish feeding by sponge-derived and pyrrole-imidazole alkaloids
    • Lindel T, Hoffmann H, Hochguertel M, Pawlik JR (2000) Structure-activity relationship of inhibition of fish feeding by sponge-derived and pyrrole-imidazole alkaloids. J Chem Ecol 26: 1477-1496
    • (2000) J Chem Ecol , vol.26 , pp. 1477-1496
    • Lindel, T.1    Hoffmann, H.2    Hochguertel, M.3    Pawlik, J.R.4
  • 41
    • 34247515502 scopus 로고    scopus 로고
    • Total synthesis of dimeric pyrrole-imidazole alkaloids: Sceptrin, ageliferin, nagelamide E, oxysceptrin, nakamuric acid, and the axinellamine carbon skeleton
    • O’Malley DP, Li K, Maue M, Zografos AL, Baran PS (2007) Total synthesis of dimeric pyrrole-imidazole alkaloids: sceptrin, ageliferin, nagelamide E, oxysceptrin, nakamuric acid, and the axinellamine carbon skeleton. J Am Chem Soc 129: 4762-4775
    • (2007) J Am Chem Soc , vol.129 , pp. 4762-4775
    • O’Malley, D.P.1    Li, K.2    Maue, M.3    Zografos, A.L.4    Baran, P.S.5
  • 42
    • 64349112135 scopus 로고    scopus 로고
    • Total synthesis of the putative structure of nagelamide D
    • Bhandari MR, Sivappa R, Lovely CJ (2009) Total synthesis of the putative structure of nagelamide D. Org Lett 11: 1535-1538
    • (2009) Org Lett , vol.11 , pp. 1535-1538
    • Bhandari, M.R.1    Sivappa, R.2    Lovely, C.J.3
  • 43
    • 0022478418 scopus 로고
    • A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine sponge Hymeniacidon sp
    • Kobayashi J, Ohizumi Y, Nakamura H, Hirata Y (1986) A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine sponge Hymeniacidon sp. Experientia 42: 1176-1177
    • (1986) Experientia , vol.42 , pp. 1176-1177
    • Kobayashi, J.1    Ohizumi, Y.2    Nakamura, H.3    Hirata, Y.4
  • 44
    • 0026043006 scopus 로고
    • The structure of clathrodin, a novel alkaloid isolated from the Caribbean Sea sponge Agelas clathrodes
    • Morales JJ, Rodriguez AD (1991) The structure of clathrodin, a novel alkaloid isolated from the Caribbean Sea sponge Agelas clathrodes. J Nat Prod 54: 629-631
    • (1991) J Nat Prod , vol.54 , pp. 629-631
    • Morales, J.J.1    Rodriguez, A.D.2
  • 46
    • 0035681520 scopus 로고    scopus 로고
    • Sventrin, a new bromopyrrole alkaloid from the Caribbean sponge Agelas sventres
    • Assmann M, Zea S, Koeck M (2001) Sventrin, a new bromopyrrole alkaloid from the Caribbean sponge Agelas sventres. J Nat Prod 64: 1593-1595
    • (2001) J Nat Prod , vol.64 , pp. 1593-1595
    • Assmann, M.1    Zea, S.2    Koeck, M.3
  • 47
    • 3042681285 scopus 로고    scopus 로고
    • Brominated pyrrole alkaloids from marine Agelas sponges reduce depolarization-induced cellular calcium elevation
    • Bickmeyer U, Drechsler C, Koeck M, AssmannM (2004) Brominated pyrrole alkaloids from marine Agelas sponges reduce depolarization-induced cellular calcium elevation. Toxicon 44: 45-51
    • (2004) Toxicon , vol.44 , pp. 45-51
    • Bickmeyer, U.1    Drechsler, C.2    Koeck, M.3    Assmann, M.4
  • 50
    • 38949088210 scopus 로고    scopus 로고
    • Debromodispacamides B and D: Isolation from the marine sponge Agelas mauritiana and stereoselective synthesis using a biomimetic proline route
    • Vergne C, Appenzeller J, Ratinaud C, Martin MT, Debitus C, Zaparucha A, Al-Mourabit A (2008) Debromodispacamides B and D: isolation from the marine sponge Agelas mauritiana and stereoselective synthesis using a biomimetic proline route. Org Lett 10: 493-496
    • (2008) Org Lett , vol.10 , pp. 493-496
    • Vergne, C.1    Appenzeller, J.2    Ratinaud, C.3    Martin, M.T.4    Debitus, C.5    Zaparucha, A.6    Al-Mourabit, A.7
  • 51
    • 0032709048 scopus 로고    scopus 로고
    • Mukanadins A-C, new bromopyrrole alkaloids from marine sponge Agelas nakamurai
    • Uemoto H, Tsuda M, Kobayashi J (1999) Mukanadins A-C, new bromopyrrole alkaloids from marine sponge Agelas nakamurai. J Nat Prod 62: 1581-1583
    • (1999) J Nat Prod , vol.62 , pp. 1581-1583
    • Uemoto, H.1    Tsuda, M.2    Kobayashi, J.3
  • 52
    • 23344447307 scopus 로고    scopus 로고
    • Bromopyrrole alkaloids from the Jamaican sponge Didiscus oxeata
    • Hu JF, Peng J, Kazi AB, Kelly M, Hamann MT (2005) Bromopyrrole alkaloids from the Jamaican sponge Didiscus oxeata. J Chem Res 7: 427-428
    • (2005) J Chem Res , vol.7 , pp. 427-428
    • Hu, J.F.1    Peng, J.2    Kazi, A.B.3    Kelly, M.4    Hamann, M.T.5
  • 54
    • 0028281686 scopus 로고
    • Mauritamide A and accompanying oroidin alkaloids from the sponge Agelas mauritiana
    • Jimenez C, Crews P (1994) Mauritamide A and accompanying oroidin alkaloids from the sponge Agelas mauritiana. Tetrahedron Lett 35: 1375-1378
    • (1994) Tetrahedron Lett , vol.35 , pp. 1375-1378
    • Jimenez, C.1    Crews, P.2
  • 55
    • 0030730152 scopus 로고    scopus 로고
    • Tauroacidins A and B, new bromopyrrole alkaloids possessing a taurine residue from Hymeniacidon sponge
    • Kobayashi J, Inaba K, Tsuda M (1997) Tauroacidins A and B, new bromopyrrole alkaloids possessing a taurine residue from Hymeniacidon sponge. Tetrahedron 53: 16679-16682
    • (1997) Tetrahedron , vol.53 , pp. 16679-16682
    • Kobayashi, J.1    Inaba, K.2    Tsuda, M.3
  • 56
    • 0034627361 scopus 로고    scopus 로고
    • Two novel pyrrole-imidazole alkaloids from the Mediterranean sponge Agelas oroides
    • Fattorusso E, Taglialatela-Scafati O (2000) Two novel pyrrole-imidazole alkaloids from the Mediterranean sponge Agelas oroides. Tetrahedron Lett 41: 9917-9922
    • (2000) Tetrahedron Lett , vol.41 , pp. 9917-9922
    • Fattorusso, E.1    Taglialatela-Scafati, O.2
  • 57
    • 0033618292 scopus 로고    scopus 로고
    • Slagenins A-C, novel bromopyrrole alkaloids from marine sponge Agelas nakamurai
    • Tsuda M, Uemoto H, Kobayashi J (1999) Slagenins A-C, novel bromopyrrole alkaloids from marine sponge Agelas nakamurai. Tetrahedron Lett 40: 5709-5712
    • (1999) Tetrahedron Lett , vol.40 , pp. 5709-5712
    • Tsuda, M.1    Uemoto, H.2    Kobayashi, J.3
  • 58
    • 37049104733 scopus 로고
    • Characterization of a yellow compound isolated from the marine sponge Phakellia flabellate
    • Sharma GM, Buyer JS, Pomerantz MW (1980) Characterization of a yellow compound isolated from the marine sponge Phakellia flabellate. J Chem Soc, Chem Commun 10: 435-436
    • (1980) J Chem Soc, Chem Commun , vol.10 , pp. 435-436
    • Sharma, G.M.1    Buyer, J.S.2    Pomerantz, M.W.3
  • 59
    • 0039430353 scopus 로고
    • 4-(2-Amino-4-oxo-2-imidazolin-5-ylidene)-2-bromo-4,5,6,7-tetrahydropyrrolo-[2,3-C] azepine _8-one Methanol solvate-a new bromo compound from the sponge Acanthella aurantiaca
    • Mattia CA, Mazzarella L, Puliti R (1982) 4-(2-Amino-4-oxo-2-imidazolin-5-ylidene)-2-bromo-4,5,6,7-tetrahydropyrrolo-[2,3-C] azepine _8-one Methanol solvate-a new bromo compound from the sponge Acanthella aurantiaca. Acta Crystallogr, Sec B, Struct Sci 38: 2513-2515
    • (1982) Acta Crystallogr, Sec B, Struct Sci , vol.38 , pp. 2513-2515
    • Mattia, C.A.1    Mazzarella, L.2    Puliti, R.3
  • 61
    • 85008131292 scopus 로고
    • Marine natural products. XII. On the chemical constituents of the Okinawan marine sponge Hymeniacidon aldis
    • Kitagawa I, Kobayashi J, Kitanaka K, Kido M, Kyogoku Y (1983) Marine natural products. XII. On the chemical constituents of the Okinawan marine sponge Hymeniacidon aldis. Chem Pharm Bull 3: 2321-2328
    • (1983) Chem Pharm Bull , vol.3 , pp. 2321-2328
    • Kitagawa, I.1    Kobayashi, J.2    Kitanaka, K.3    Kido, M.4    Kyogoku, Y.5
  • 64
    • 0030971562 scopus 로고    scopus 로고
    • Z-axinohydantoin and debromo-Z-axinohydantoin from the sponge Stylotella aurantium: Inhibitors of protein kinase C
    • Patil AD, Freyer AJ, Killmer L, Hofmann G, Randall K (1997) Z-axinohydantoin and debromo-Z-axinohydantoin from the sponge Stylotella aurantium: inhibitors of protein kinase C. Nat Prod Lett 9: 201-207
    • (1997) Nat Prod Lett , vol.9 , pp. 201-207
    • Patil, A.D.1    Freyer, A.J.2    Killmer, L.3    Hofmann, G.4    Randall, K.5
  • 65
    • 0031775784 scopus 로고    scopus 로고
    • Spongiacidins A-D, new bromopyrrole alkaloids from Hymeniacidon sponge
    • Inaba K, Sato H, Tsuda M, Kobayashi J (1998) Spongiacidins A-D, new bromopyrrole alkaloids from Hymeniacidon sponge. J Nat Prod 61: 693-695
    • (1998) J Nat Prod , vol.61 , pp. 693-695
    • Inaba, K.1    Sato, H.2    Tsuda, M.3    Kobayashi, J.4
  • 66
    • 10544237275 scopus 로고    scopus 로고
    • Isomers and tautomers of hymenialdisine and debromohymenialdisine
    • Williams DH, Faulkner DJ (1996) Isomers and tautomers of hymenialdisine and debromohymenialdisine. Nat Prod Lett 9: 57-64
    • (1996) Nat Prod Lett , vol.9 , pp. 57-64
    • Williams, D.H.1    Faulkner, D.J.2
  • 67
    • 0022545106 scopus 로고
    • Hymenin, an a-adrenoceptor blocking agent from the Okinawan marine sponge Hymeniacidon sp
    • Kobayashi J, Ohizumi Y, Nakamura H, Hirata Y, Wakamatsu K, Miyazawa T (1986) Hymenin, an a-adrenoceptor blocking agent from the Okinawan marine sponge Hymeniacidon sp. Experientia 42: 1064-1065
    • (1986) Experientia , vol.42 , pp. 1064-1065
    • Kobayashi, J.1    Ohizumi, Y.2    Nakamura, H.3    Hirata, Y.4    Wakamatsu, K.5    Miyazawa, T.6
  • 68
    • 45949131479 scopus 로고
    • Marine invertebrate of Neo-Caledonian V. Isolation and identification of the metabolites of the new Caledonian sponge Pseudaxinyssa cantharella
    • De Nanteuil G, Ahond A, Guilhem J, Poupat C, Tran Huu Dau E, Potier P, Pusset M, Pusset J, Laboute P (1985) Marine invertebrate of Neo-Caledonian V. Isolation and identification of the metabolites of the new Caledonian sponge Pseudaxinyssa cantharella. Tetrahedron 41: 6019-6033
    • (1985) Tetrahedron , vol.41 , pp. 6019-6033
    • De Nanteuil, G.1    Ahond, A.2    Guilhem, J.3    Poupat, C.4    Tran Huu Dau, E.5    Potier, P.6    Pusset, M.7    Pusset, J.8    Laboute, P.9
  • 70
    • 0032760487 scopus 로고    scopus 로고
    • Chemical defense of the Caribbean reef sponge Axinella corrugata against predatory fishes
    • Wilson DM, Puyana M, Fenical W, Pawlik JR (1999) Chemical defense of the Caribbean reef sponge Axinella corrugata against predatory fishes. J Chem Ecol 25: 2811-2823
    • (1999) J Chem Ecol , vol.25 , pp. 2811-2823
    • Wilson, D.M.1    Puyana, M.2    Fenical, W.3    Pawlik, J.R.4
  • 72
    • 0033958644 scopus 로고    scopus 로고
    • Potential role of glycogen synthase kinase-3 in skeletal muscle insulin resistance of type 2 diabetes
    • Nikoulina SE, Ciaraldi TP, Mudaliar S, Mohideen P, Carter L, Henry RR (2000) Potential role of glycogen synthase kinase-3 in skeletal muscle insulin resistance of type 2 diabetes. Diabetes 49: 263-271
    • (2000) Diabetes , vol.49 , pp. 263-271
    • Nikoulina, S.E.1    Ciaraldi, T.P.2    Mudaliar, S.3    Mohideen, P.4    Carter, L.5    Henry, R.R.6
  • 73
    • 0036273020 scopus 로고    scopus 로고
    • Glycogen synthase kinase (GSK-3) inhibitors as new promising drugs for diabetes, neurodegeneration, cancer and inflammation
    • Martinez A, Castro A, Dorronsoro I, Alonso M (2002) Glycogen synthase kinase (GSK-3) inhibitors as new promising drugs for diabetes, neurodegeneration, cancer and inflammation. Med Res Rev 22: 373-384
    • (2002) Med Res Rev , vol.22 , pp. 373-384
    • Martinez, A.1    Castro, A.2    Dorronsoro, I.3    Alonso, M.4
  • 74
    • 3042599015 scopus 로고    scopus 로고
    • Inhibition of cytokine production by hymenialdisine derivatives
    • Sharma V, Lansdell TA, Jin G, Tepe JJ (2004) Inhibition of cytokine production by hymenialdisine derivatives. J Med Chem 47: 3700-3703
    • (2004) J Med Chem , vol.47 , pp. 3700-3703
    • Sharma, V.1    Lansdell, T.A.2    Jin, G.3    Tepe, J.J.4
  • 75
    • 70350738510 scopus 로고    scopus 로고
    • Preparation of hymenialdisine, analogues and their evaluation as kinase inhibitors
    • Nguyen TNT, Tepe JJ (2009) Preparation of hymenialdisine, analogues and their evaluation as kinase inhibitors. Curr Med Chem 16: 3122-3143
    • (2009) Curr Med Chem , vol.16 , pp. 3122-3143
    • Nguyen, T.N.T.1    Tepe, J.J.2
  • 77
    • 0142068213 scopus 로고
    • Structure of dibromophakellin, a new brominecontaining alkaloid from the marine sponge Phakellia flabellate
    • Sharma GM, Burkholder PR (1971) Structure of dibromophakellin, a new brominecontaining alkaloid from the marine sponge Phakellia flabellate. J Chem Soc D Chem Commun 3: 151-152
    • (1971) J Chem Soc D Chem Commun , vol.3 , pp. 151-152
    • Sharma, G.M.1    Burkholder, P.R.2
  • 78
    • 4344678685 scopus 로고    scopus 로고
    • An analysis of phakellin and oroidin structure stimulated by further study of an Agelas sponge
    • Gautschi JT, Whitman S, Holman TR, Crews P (2004) An analysis of phakellin and oroidin structure stimulated by further study of an Agelas sponge. J Nat Prod 67: 1256-1261
    • (2004) J Nat Prod , vol.67 , pp. 1256-1261
    • Gautschi, J.T.1    Whitman, S.2    Holman, T.R.3    Crews, P.4
  • 79
    • 0031019142 scopus 로고    scopus 로고
    • Antineoplastic agents. 362. Isolation and X-ray crystal structure of dibromophakellistatin from the Indian Ocean sponge Phakellia mauritiana
    • Pettit GR, McNulty J, Herald DL, Doubek DL, Chapuis JC, Schmidt JM, Tackett LP, Boyd MR (1997) Antineoplastic agents. 362. Isolation and X-ray crystal structure of dibromophakellistatin from the Indian Ocean sponge Phakellia mauritiana. J Nat Prod 60: 180-183
    • (1997) J Nat Prod , vol.60 , pp. 180-183
    • Pettit, G.R.1    McNulty, J.2    Herald, D.L.3    Doubek, D.L.4    Chapuis, J.C.5    Schmidt, J.M.6    Tackett, L.P.7    Boyd, M.R.8
  • 81
    • 0027212254 scopus 로고
    • Palau’amine: A cytotoxic and immunosuppressive hexacyclic bisguanidine antibiotic from the sponge Stylotella agminata
    • Kinnel RB, Gehrken HP, Scheuer PJ (1993) Palau’amine: a cytotoxic and immunosuppressive hexacyclic bisguanidine antibiotic from the sponge Stylotella agminata. J Am Chem Soc 115: 3376-3377
    • (1993) J Am Chem Soc , vol.115 , pp. 3376-3377
    • Kinnel, R.B.1    Gehrken, H.P.2    Scheuer, P.J.3
  • 82
    • 0032524819 scopus 로고    scopus 로고
    • Palau’amine and its congeners: A family of bioactive bisguanidines from the marine sponge Stylotella aurantium
    • Kinnel RB, Gehrken HP, Swali R, Skoropowski G, Scheuer PJ (1998) Palau’amine and its congeners: a family of bioactive bisguanidines from the marine sponge Stylotella aurantium. J Org Chem 63: 3281-3286
    • (1998) J Org Chem , vol.63 , pp. 3281-3286
    • Kinnel, R.B.1    Gehrken, H.P.2    Swali, R.3    Skoropowski, G.4    Scheuer, P.J.5
  • 83
    • 0028936559 scopus 로고
    • Styloguanidines, new chitinase inhibitors from the marine sponge Stylotella aurantium
    • Kato T, Shizuri Y, Izumida H, Yokoyama A, Endo M (1995) Styloguanidines, new chitinase inhibitors from the marine sponge Stylotella aurantium. Tetrahedron Lett 36: 2133-2136
    • (1995) Tetrahedron Lett , vol.36 , pp. 2133-2136
    • Kato, T.1    Shizuri, Y.2    Izumida, H.3    Yokoyama, A.4    Endo, M.5
  • 84
    • 0027170397 scopus 로고
    • Agelastatin A, a new skeleton cytotoxic alkaloid of the oroidin family. Isolation from the Axinellid sponge Agelas dendromorpha of the Coral Sea
    • D’Ambrosio M, Guerriero A, Debitus C, Ribes O, Pusset J, Leroy S, Pietra F (1993) Agelastatin A, a new skeleton cytotoxic alkaloid of the oroidin family. Isolation from the Axinellid sponge Agelas dendromorpha of the Coral Sea. J Chem Soc Chem Commun 16: 1305-1306
    • (1993) J Chem Soc Chem Commun , vol.16 , pp. 1305-1306
    • D’Ambrosio, M.1    Guerriero, A.2    Debitus, C.3    Ribes, O.4    Pusset, J.5    Leroy, S.6    Pietra, F.7
  • 85
    • 0029904176 scopus 로고    scopus 로고
    • 65. The active centers of agelastatin A, a strongly cytotoxic alkaloid of the Coral Sea Axinellid sponge Agelas dendromorpha, as determined by comparative bioassays with semisynthetic derivatives
    • D’Ambrosio M, Guerriero A, Ripamonti M, Debitus C, Waikedre J, Pietra F (1996) 65. The active centers of agelastatin A, a strongly cytotoxic alkaloid of the Coral Sea Axinellid sponge Agelas dendromorpha, as determined by comparative bioassays with semisynthetic derivatives. Helv Chim Acta 79: 727-735
    • (1996) Helv Chim Acta , vol.79 , pp. 727-735
    • D’Ambrosio, M.1    Guerriero, A.2    Ripamonti, M.3    Debitus, C.4    Waikedre, J.5    Pietra, F.6
  • 86
    • 0031886176 scopus 로고    scopus 로고
    • Agelastatins C and D, new pentacyclic bromopyrroles from the sponge Cymbastela sp., and potent anthropod toxicity of (-)-agelastatin A
    • Hong TW, Jimenez DR, Molinski TF (1998) Agelastatins C and D, new pentacyclic bromopyrroles from the sponge Cymbastela sp., and potent anthropod toxicity of (-)-agelastatin A. J Nat Prod 61: 158-161
    • (1998) J Nat Prod , vol.61 , pp. 158-161
    • Hong, T.W.1    Jimenez, D.R.2    Molinski, T.F.3
  • 87
    • 33749012529 scopus 로고    scopus 로고
    • Agesamides A and B, bromopyrrole alkaloids from sponge Agelas species: Application of DOSY for chemical screening of new metabolites
    • Tsuda M, Yasuda T, Fukushi E, Kawabata J, Sekiguchi M, Fromont J, Kobayashi J (2006) Agesamides A and B, bromopyrrole alkaloids from sponge Agelas species: application of DOSY for chemical screening of new metabolites. Org Lett 8: 4235-4238
    • (2006) Org Lett , vol.8 , pp. 4235-4238
    • Tsuda, M.1    Yasuda, T.2    Fukushi, E.3    Kawabata, J.4    Sekiguchi, M.5    Fromont, J.6    Kobayashi, J.7
  • 88
    • 33748806602 scopus 로고    scopus 로고
    • Oxocyclostylidol, an intramolecular cyclized oroidin derivative from the marine sponge Stylissa caribica
    • Grube A, Koeck M (2006) Oxocyclostylidol, an intramolecular cyclized oroidin derivative from the marine sponge Stylissa caribica. J Nat Prod 69: 1212-1214
    • (2006) J Nat Prod , vol.69 , pp. 1212-1214
    • Grube, A.1    Koeck, M.2
  • 89
    • 0028804014 scopus 로고
    • Longamide and 3,7-dimethylisoguanine, two novel alkaloids from the marine sponge Agelas longissima
    • Cafieri F, Fattorusso E, Mangoni A, Taglialatela-Scafati O (1995) Longamide and 3,7-dimethylisoguanine, two novel alkaloids from the marine sponge Agelas longissima. Tetrahedron Lett 36: 7893-7896
    • (1995) Tetrahedron Lett , vol.36 , pp. 7893-7896
    • Cafieri, F.1    Fattorusso, E.2    Mangoni, A.3    Taglialatela-Scafati, O.4
  • 90
    • 0031947168 scopus 로고    scopus 로고
    • A new lysine derivative and new 3-bromopyrrole carboxylic acid derivative from two marine sponges
    • Li CJ, Schmitz FJ, Kelly-Borges M (1998) A new lysine derivative and new 3-bromopyrrole carboxylic acid derivative from two marine sponges. J Nat Prod 61: 387-289
    • (1998) J Nat Prod , vol.61 , pp. 387
    • Li, C.J.1    Schmitz, F.J.2    Kelly-Borges, M.3
  • 92
    • 84897509896 scopus 로고    scopus 로고
    • New bromopyrrole alkaloids from the marine sponges Axinella damicornis and Stylissa flabelliformis
    • Hassan W, Elkhayat E, Edrada R, Ebel R, Proksch P (2007) New bromopyrrole alkaloids from the marine sponges Axinella damicornis and Stylissa flabelliformis. Nat Prod Commun 2: 1-6
    • (2007) Nat Prod Commun , vol.2 , pp. 1-6
    • Hassan, W.1    Elkhayat, E.2    Edrada, R.3    Ebel, R.4    Proksch, P.5
  • 93
    • 0031909711 scopus 로고    scopus 로고
    • Novel bromopyrrole alkaloids from the sponge Agelas dispar
    • Cafieri F, Fattorusso E, Taglialatela-Scafati O (1998) Novel bromopyrrole alkaloids from the sponge Agelas dispar. J Nat Prod 61: 122-125
    • (1998) J Nat Prod , vol.61 , pp. 122-125
    • Cafieri, F.1    Fattorusso, E.2    Taglialatela-Scafati, O.3
  • 94
    • 0030877326 scopus 로고    scopus 로고
    • Hanishin, a semiracemic, bioactive C9 alkaloid of the Axinellid sponge Acanthella carteri from the Hanish Islands
    • Mancini I, Guella G, Amade P, Roussakis C, Pietra F (1997) Hanishin, a semiracemic, bioactive C9 alkaloid of the Axinellid sponge Acanthella carteri from the Hanish Islands. A shunt metabolite? Tetrahedron Lett 38: 6271-6274
    • (1997) A shunt metabolite? Tetrahedron Lett , vol.38 , pp. 6271-6274
    • Mancini, I.1    Guella, G.2    Amade, P.3    Roussakis, C.4    Pietra, F.5
  • 95
    • 0031730201 scopus 로고    scopus 로고
    • A new bromopyrrole alkaloid and the optical resolution of the racemate from the marine sponge Homaxinella sp
    • Umeyama A, Ito S, Yuasa E, Arihara S, Yamada T (1998) A new bromopyrrole alkaloid and the optical resolution of the racemate from the marine sponge Homaxinella sp. J Nat Prod 61: 1433-1434
    • (1998) J Nat Prod , vol.61 , pp. 1433-1434
    • Umeyama, A.1    Ito, S.2    Yuasa, E.3    Arihara, S.4    Yamada, T.5
  • 96
    • 0024421660 scopus 로고
    • Immunosuppressive compounds from a deep water marine sponge, Agelas flabelliformis
    • Gunasekera SP, Cranick S, Longley RE (1989) Immunosuppressive compounds from a deep water marine sponge, Agelas flabelliformis. J Nat Prod 52: 757-761
    • (1989) J Nat Prod , vol.52 , pp. 757-761
    • Gunasekera, S.P.1    Cranick, S.2    Longley, R.E.3
  • 99
    • 0019825508 scopus 로고
    • Sceptrin, an antimicrobial agent from the sponge Agelas sceptrum
    • Walker RP, Faulkner DJ (1981) Sceptrin, an antimicrobial agent from the sponge Agelas sceptrum. J Am Chem Soc 103: 6772-6773
    • (1981) J Am Chem Soc , vol.103 , pp. 6772-6773
    • Walker, R.P.1    Faulkner, D.J.2
  • 102
    • 33750366010 scopus 로고    scopus 로고
    • Stylissadines A and B: The first tetrameric pyrrole-imidazole alkaloids
    • Grube A, Koeck M (2006) Stylissadines A and B: the first tetrameric pyrrole-imidazole alkaloids. Org Lett 8: 4675-4678
    • (2006) Org Lett , vol.8 , pp. 4675-4678
    • Grube, A.1    Koeck, M.2
  • 104
    • 0030783964 scopus 로고    scopus 로고
    • Konbu’acidin A, a new bromopyrrole alkaloid with cdk4 inhibitory activity from Hymeniacidon sponge
    • Kobayashi J, Suzuki M, Tsuda M (1997) Konbu’acidin A, a new bromopyrrole alkaloid with cdk4 inhibitory activity from Hymeniacidon sponge. Tetrahedron 53: 15681-15684
    • (1997) Tetrahedron , vol.53 , pp. 15681-15684
    • Kobayashi, J.1    Suzuki, M.2    Tsuda, M.3
  • 105
    • 0001759287 scopus 로고
    • Biologically active marine natural products
    • Rinehart KL (1989) Biologically active marine natural products. Pure Appl Chem 61: 525-528
    • (1989) Pure Appl Chem , vol.61 , pp. 525-528
    • Rinehart, K.L.1
  • 107
    • 15044362347 scopus 로고    scopus 로고
    • Bromoageliferin and dibromoageliferin, secondary metabolites from the marine sponge Agelas conifera, inhibit voltage-operated, but not store-operated calcium entry in PC12 cells
    • Bickmeyer U (2005) Bromoageliferin and dibromoageliferin, secondary metabolites from the marine sponge Agelas conifera, inhibit voltage-operated, but not store-operated calcium entry in PC12 cells. Toxicon 45: 627-632
    • (2005) Toxicon , vol.45 , pp. 627-632
    • Bickmeyer, U.1
  • 108
    • 0029925442 scopus 로고    scopus 로고
    • N-methylated ageliferins from the sponge Astrosclera willeyana from Pohnepi
    • Williams DH, Faulkner DJ (1996) N-methylated ageliferins from the sponge Astrosclera willeyana from Pohnepi. Tetrahedron 52: 5381-5390
    • (1996) Tetrahedron , vol.52 , pp. 5381-5390
    • Williams, D.H.1    Faulkner, D.J.2
  • 110
    • 34250822266 scopus 로고    scopus 로고
    • Nagelamide J, a novel dimeric bromopyrrole alkaloid from a sponge Agelas species
    • Araki A, Tsuda M, Kubota T, Mikami Y, Fromont J, Kobayashi J (2007) Nagelamide J, a novel dimeric bromopyrrole alkaloid from a sponge Agelas species. Org Lett 9: 2369-2371
    • (2007) Org Lett , vol.9 , pp. 2369-2371
    • Araki, A.1    Tsuda, M.2    Kubota, T.3    Mikami, Y.4    Fromont, J.5    Kobayashi, J.6
  • 111
    • 49349087664 scopus 로고    scopus 로고
    • Nagelamides K and L, dimeric bromopyrrole alkaloids from sponge Agelas species
    • Araki A, Kubota T, Tsuda M, Mikami Y, Fromont J, Kobayashi J (2008) Nagelamides K and L, dimeric bromopyrrole alkaloids from sponge Agelas species. Org Lett 10: 2099-2102
    • (2008) Org Lett , vol.10 , pp. 2099-2102
    • Araki, A.1    Kubota, T.2    Tsuda, M.3    Mikami, Y.4    Fromont, J.5    Kobayashi, J.6
  • 113
    • 65249148666 scopus 로고    scopus 로고
    • Nagelamides Q and R, novel dimeric bromopyrrole alkaloids from sponges Agelas sp
    • Araki A, Kubota T, Aoyama K, Mikami Y, Fromont J, Kobayashi J (2009) Nagelamides Q and R, novel dimeric bromopyrrole alkaloids from sponges Agelas sp. Org Lett 11: 1785-1788
    • (2009) Org Lett , vol.11 , pp. 1785-1788
    • Araki, A.1    Kubota, T.2    Aoyama, K.3    Mikami, Y.4    Fromont, J.5    Kobayashi, J.6
  • 114
    • 37049126595 scopus 로고
    • Aerplysinin-1, a new bromo-compound from Aplysina aerophoba
    • Fattorusso E, Minale L, Sodano G (1970) Aerplysinin-1, a new bromo-compound from Aplysina aerophoba. Chem Commun 12: 751-752
    • (1970) Chem Commun , vol.12 , pp. 751-752
    • Fattorusso, E.1    Minale, L.2    Sodano, G.3
  • 115
    • 0006440932 scopus 로고
    • 2-Hydroxy, 3,5-dibromo, 4-methoxyphenylacetamide. A dibromotyrosine metabolite from Psammoposilla purpurea
    • Chang CWJ, Weinheimer AJ (1977) 2-Hydroxy, 3,5-dibromo, 4-methoxyphenylacetamide. A dibromotyrosine metabolite from Psammoposilla purpurea. Tetrahedron Lett 18: 4005-4008
    • (1977) Tetrahedron Lett , vol.18 , pp. 4005-4008
    • Chang, C.W.J.1    Weinheimer, A.J.2
  • 116
    • 84970589329 scopus 로고
    • Two epimeric dibromo nitriles from the Australian sponge Aplysina laevis
    • Capon RJ, Macleod JK (1987) Two epimeric dibromo nitriles from the Australian sponge Aplysina laevis. Austr J Chem 40: 341-346
    • (1987) Austr J Chem , vol.40 , pp. 341-346
    • Capon, R.J.1    Macleod, J.K.2
  • 118
    • 0014870524 scopus 로고
    • Isolation and absolute configuration of the aeroplysinin-1 enantiomorphic pair from Ianthella ardis
    • Fulmor W, van Lear GE, Morton GO, Mills RD (1970) Isolation and absolute configuration of the aeroplysinin-1 enantiomorphic pair from Ianthella ardis. Tetrahedron Lett 11: 4551-4552
    • (1970) Tetrahedron Lett , vol.11 , pp. 4551-4552
    • Fulmor, W.1    van Lear, G.E.2    Morton, G.O.3    Mills, R.D.4
  • 120
    • 0027692681 scopus 로고
    • Antibiotic and cytotoxic activity of brominated compounds from the marine sponge Verongia aerophoba
    • Teeyapant R, Woerdenbag HJ, Kreis P, Hacker J, Wray V, Witte L, Proksch P (1993) Antibiotic and cytotoxic activity of brominated compounds from the marine sponge Verongia aerophoba. Z Naturforsch 48c: 939-945
    • (1993) Z Naturforsch , vol.48 c , pp. 939-945
    • Teeyapant, R.1    Woerdenbag, H.J.2    Kreis, P.3    Hacker, J.4    Wray, V.5    Witte, L.6    Proksch, P.7
  • 123
    • 0027306808 scopus 로고
    • Biotransformation of brominated compounds in the marine sponge Verongia aerophoba-Evidence for an induced chemical defense?
    • Teeyapant R, Proksch P (1993) Biotransformation of brominated compounds in the marine sponge Verongia aerophoba-Evidence for an induced chemical defense? Naturwissenschaften 80: 369-370
    • (1993) Naturwissenschaften , vol.80 , pp. 369-370
    • Teeyapant, R.1    Proksch, P.2
  • 125
    • 0030770048 scopus 로고    scopus 로고
    • Wound activation of protoxins in marine sponge Aplysina aerophoba
    • Ebel R, Brenzinger M, Kunze A, Gross HJ, Proksch P (1997) Wound activation of protoxins in marine sponge Aplysina aerophoba. J Chem Ecol 23: 1451-1462
    • (1997) J Chem Ecol , vol.23 , pp. 1451-1462
    • Ebel, R.1    Brenzinger, M.2    Kunze, A.3    Gross, H.J.4    Proksch, P.5
  • 126
    • 33644919455 scopus 로고    scopus 로고
    • Activated chemical defense in Aplysina sponges revisited
    • Thoms C, Ebel R, Proksch P (2006) Activated chemical defense in Aplysina sponges revisited. J Chem Ecol 32: 97-123
    • (2006) J Chem Ecol , vol.32 , pp. 97-123
    • Thoms, C.1    Ebel, R.2    Proksch, P.3
  • 128
    • 0031690667 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of aeroplysinin analogues: A new class of receptor tyrosine kinase inhibitors
    • Hinterding K, Knebel A, Herrlich P, Waldmann H (1998) Synthesis and biological evaluation of aeroplysinin analogues: a new class of receptor tyrosine kinase inhibitors. Bioorg Med Chem 6: 1153-1162
    • (1998) Bioorg Med Chem , vol.6 , pp. 1153-1162
    • Hinterding, K.1    Knebel, A.2    Herrlich, P.3    Waldmann, H.4
  • 129
    • 0025160184 scopus 로고
    • Inhibition of intrinsic protein tyrosine kinase activity of EGF-receptor kinase complex from human breast cancer cells by the marine sponge metabolite (+)-aeroplysinin-1
    • Kreuter MH, Leake RE, Rinaldl F, Mueller-Klieser W, Maidhof A, Mueller WEG, Schroeder HC (1990) Inhibition of intrinsic protein tyrosine kinase activity of EGF-receptor kinase complex from human breast cancer cells by the marine sponge metabolite (+)-aeroplysinin-1. Comp Biochem Physiol 97B: 151-158
    • (1990) Comp Biochem Physiol , vol.97 B , pp. 151-158
    • Kreuter, M.H.1    Leake, R.E.2    Rinaldl, F.3    Mueller-Klieser, W.4    Maidhof, A.5    Mueller, W.E.G.6    Schroeder, H.C.7
  • 130
    • 0000055673 scopus 로고
    • Phenolic constituents of Psammaplysilla
    • Quiňoà E, Crews P (1987) Phenolic constituents of Psammaplysilla. Tetrahedron Lett 28: 3229-3232
    • (1987) Tetrahedron Lett , vol.28 , pp. 3229-3232
    • Quiňoà, E.1    Crews, P.2
  • 131
    • 0023636076 scopus 로고
    • Two bromotyrosine-cysteine derived metabolites from a sponge
    • Rodríguez AD, Akee RK, Scheuer PJ (1987) Two bromotyrosine-cysteine derived metabolites from a sponge. Tetrahedron Lett 28: 4989-4992
    • (1987) Tetrahedron Lett , vol.28 , pp. 4989-4992
    • Rodríguez, A.D.1    Akee, R.K.2    Scheuer, P.J.3
  • 132
    • 0000529638 scopus 로고    scopus 로고
    • Isolation of psammaplin A 11'-sulfate and bisaprasin 11'-sulfate from the marine sponge Aplysinella rhax
    • Pham NB, Butler MS, Quinn RJ (2000) Isolation of psammaplin A 11'-sulfate and bisaprasin 11'-sulfate from the marine sponge Aplysinella rhax. J Nat Prod 63: 393-395
    • (2000) J Nat Prod , vol.63 , pp. 393-395
    • Pham, N.B.1    Butler, M.S.2    Quinn, R.J.3
  • 134
    • 0344549834 scopus 로고    scopus 로고
    • New bromotyrosine derivatives from an association of two sponges, Jaspis wondoensis and Poecillastra wondoensis
    • Park Y, Liu Y, Hong J, Lee CO, Cho H, Kim DK, Im KS, Jung JH (2003) New bromotyrosine derivatives from an association of two sponges, Jaspis wondoensis and Poecillastra wondoensis. J Nat Prod 66: 1495-1498
    • (2003) J Nat Prod , vol.66 , pp. 1495-1498
    • Park, Y.1    Liu, Y.2    Hong, J.3    Lee, C.O.4    Cho, H.5    Kim, D.K.6    Im, K.S.7    Jung, J.H.8
  • 135
    • 56249138249 scopus 로고    scopus 로고
    • Cytotoxic bromotyrosine derivatives from a two-sponge association of Jaspis sp. and Poecillastra sp
    • Shinde PB, Lee YM, Dang HT, Hong J, Lee CO, Jung JH (2008) Cytotoxic bromotyrosine derivatives from a two-sponge association of Jaspis sp. and Poecillastra sp. Bioorg Med Chem Lett 18: 6414-6418
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 6414-6418
    • Shinde, P.B.1    Lee, Y.M.2    Dang, H.T.3    Hong, J.4    Lee, C.O.5    Jung, J.H.6
  • 137
    • 0034634603 scopus 로고    scopus 로고
    • New bromotyrosine metabolites from the sponge Aplysinella rhax
    • Shin J, Lee HS, Seo Y, Rho JR, Cho KW, Paul VJ (2000) New bromotyrosine metabolites from the sponge Aplysinella rhax. Tetrahedron 56: 9071-9077
    • (2000) Tetrahedron , vol.56 , pp. 9071-9077
    • Shin, J.1    Lee, H.S.2    Seo, Y.3    Rho, J.R.4    Cho, K.W.5    Paul, V.J.6
  • 139
    • 0346094302 scopus 로고    scopus 로고
    • Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro
    • Shim JS, Lee HS, Shin J, Kwon HJ (2004) Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro. Cancer Lett 203: 163-169
    • (2004) Cancer Lett , vol.203 , pp. 163-169
    • Shim, J.S.1    Lee, H.S.2    Shin, J.3    Kwon, H.J.4
  • 140
    • 0033073547 scopus 로고    scopus 로고
    • Psammaplin A, a natural bromotyrosine derivative from a sponge, possesses the antibacterial activity against methicillin-resistant Staphylococcous aureus and the DNA gyrase-inhibitory activity
    • Kim D, Lee IS, Jung JH, Yang SI (1999) Psammaplin A, a natural bromotyrosine derivative from a sponge, possesses the antibacterial activity against methicillin-resistant Staphylococcous aureus and the DNA gyrase-inhibitory activity. Arch Pharm Res 22: 25-29
    • (1999) Arch Pharm Res , vol.22 , pp. 25-29
    • Kim, D.1    Lee, I.S.2    Jung, J.H.3    Yang, S.I.4
  • 141
    • 33744500224 scopus 로고    scopus 로고
    • Bioassay for the identification of natural product-based activators of peroxisome proliferator-activated receptor-g (PPARg): The marine sponge metabolite psammaplin A activates PPARg and induces apoptosis in human breast tumor cells
    • Mora FD, Jones DK, Desai PV, Patny A, Avery MA, Feller DR, Smillie T, Zhou YD, Nagle DG (2006) Bioassay for the identification of natural product-based activators of peroxisome proliferator-activated receptor-g (PPARg): The marine sponge metabolite psammaplin A activates PPARg and induces apoptosis in human breast tumor cells. J Nat Prod 69: 547-552
    • (2006) J Nat Prod , vol.69 , pp. 547-552
    • Mora, F.D.1    Jones, D.K.2    Desai, P.V.3    Patny, A.4    Avery, M.A.5    Feller, D.R.6    Smillie, T.7    Zhou, Y.D.8    Nagle, D.G.9
  • 143
    • 33847657556 scopus 로고    scopus 로고
    • Psammaplin A is a natural prodrug that inhibits class I histone deacetylase
    • Kim DH, Shin J, Kwon HJ (2007) Psammaplin A is a natural prodrug that inhibits class I histone deacetylase. Exp Mol Med 39: 47-55
    • (2007) Exp Mol Med , vol.39 , pp. 47-55
    • Kim, D.H.1    Shin, J.2    Kwon, H.J.3
  • 144
    • 37349061341 scopus 로고    scopus 로고
    • A natural histone deacetylase inhibitor, psammaplin A, induces cell cycle arrest and apoptosis in human endometrial cancer cells
    • Ahn MY, Jung JH, Na YJ, Kim HS (2008) A natural histone deacetylase inhibitor, psammaplin A, induces cell cycle arrest and apoptosis in human endometrial cancer cells. Gynecol Oncol 108: 27-33
    • (2008) Gynecol Oncol , vol.108 , pp. 27-33
    • Ahn, M.Y.1    Jung, J.H.2    Na, Y.J.3    Kim, H.S.4
  • 146
    • 0035477708 scopus 로고    scopus 로고
    • Optimization and mechanistic studies of psammaplin A type antibacterial agents active against methicillin-resistant Staphylococcus aureus (MRSA)
    • Nicolaou KC, Hughes R, Pfefferkorn JA, Barluenga S (2001) Optimization and mechanistic studies of psammaplin A type antibacterial agents active against methicillin-resistant Staphylococcus aureus (MRSA). Chem Eur J 7: 4296-4310
    • (2001) Chem Eur J , vol.7 , pp. 4296-4310
    • Nicolaou, K.C.1    Hughes, R.2    Pfefferkorn, J.A.3    Barluenga, S.4
  • 147
    • 0025881628 scopus 로고
    • Purealidin A, a new cytotoxic bromotyrosine-derived alkaloid from the Okinawan marine sponge Psammaplysilla purea
    • Ishibashi M, Tsuda M, Ohizumi Y, Sasaki T, Kobayashi J (1991) Purealidin A, a new cytotoxic bromotyrosine-derived alkaloid from the Okinawan marine sponge Psammaplysilla purea. Experientia 47: 299-300
    • (1991) Experientia , vol.47 , pp. 299-300
    • Ishibashi, M.1    Tsuda, M.2    Ohizumi, Y.3    Sasaki, T.4    Kobayashi, J.5
  • 148
    • 0025766030 scopus 로고
    • Purealidins B and C, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea
    • Kobayashi J, Tsuda M, Agemi K, Shigemori H, Ishibashi M, Sasaki T, Mikami Y (1991) Purealidins B and C, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea. Tetrahedron 47: 6617-6622
    • (1991) Tetrahedron , vol.47 , pp. 6617-6622
    • Kobayashi, J.1    Tsuda, M.2    Agemi, K.3    Shigemori, H.4    Ishibashi, M.5    Sasaki, T.6    Mikami, Y.7
  • 149
    • 0026514347 scopus 로고
    • Purealidin D, a new pyridine alkaloid from the Okinawan marine sponge Psammaplysilla purea
    • Tsuda M, Shigemori H, Ishibashi M, Kobayashi J (1992) Purealidin D, a new pyridine alkaloid from the Okinawan marine sponge Psammaplysilla purea. Tetrahedron Lett 33: 2597-2598
    • (1992) Tetrahedron Lett , vol.33 , pp. 2597-2598
    • Tsuda, M.1    Shigemori, H.2    Ishibashi, M.3    Kobayashi, J.4
  • 150
    • 0026645943 scopus 로고
    • Purealidins E-G, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea
    • Tsuda M, Shigemori H, Ishibashi M, Kobayashi J (1992) Purealidins E-G, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea. J Nat Prod 55: 1325-1327
    • (1992) J Nat Prod , vol.55 , pp. 1325-1327
    • Tsuda, M.1    Shigemori, H.2    Ishibashi, M.3    Kobayashi, J.4
  • 151
    • 0029032407 scopus 로고
    • Lipopurealidins D and E and purealidin H, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea
    • Kobayashi J, Honma K, Tsuda M, Kosaka T (1995) Lipopurealidins D and E and purealidin H, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea. J Nat Prod 58: 467-470
    • (1995) J Nat Prod , vol.58 , pp. 467-470
    • Kobayashi, J.1    Honma, K.2    Tsuda, M.3    Kosaka, T.4
  • 152
    • 0028913755 scopus 로고
    • Purealidins J-R, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea
    • Kobayashi J, Honma H, Sasaki T, Tsuda M (1995) Purealidins J-R, new bromotyrosine alkaloids from the Okinawan marine sponge Psammaplysilla purea. Chem Pharm Bull 43: 403-407
    • (1995) Chem Pharm Bull , vol.43 , pp. 403-407
    • Kobayashi, J.1    Honma, H.2    Sasaki, T.3    Tsuda, M.4
  • 153
    • 0036932559 scopus 로고    scopus 로고
    • Purealidin S and purpuramine J, bromotyrosine alkaloids from the Fijian marine sponge Druinella sp
    • Tabudravu JN, Jaspars M (2002) Purealidin S and purpuramine J, bromotyrosine alkaloids from the Fijian marine sponge Druinella sp. J Nat Prod 65: 1798-1801
    • (2002) J Nat Prod , vol.65 , pp. 1798-1801
    • Tabudravu, J.N.1    Jaspars, M.2
  • 155
    • 17844365847 scopus 로고    scopus 로고
    • The psammaplysenes, specific inhibitors of FOXO1a nuclear export
    • Schroeder FC, Kau TR, Silver PA, Clardy J (2005) The psammaplysenes, specific inhibitors of FOXO1a nuclear export. J Nat Prod 68: 574-576
    • (2005) J Nat Prod , vol.68 , pp. 574-576
    • Schroeder, F.C.1    Kau, T.R.2    Silver, P.A.3    Clardy, J.4
  • 157
    • 25444454350 scopus 로고    scopus 로고
    • Total synthesis of psammaplysenes A and B, naturally occurring inhibitors of FOXO1a nuclear export
    • Georgiades SN, Clardy J (2005) Total synthesis of psammaplysenes A and B, naturally occurring inhibitors of FOXO1a nuclear export. Org Lett 7: 4091-4094
    • (2005) Org Lett , vol.7 , pp. 4091-4094
    • Georgiades, S.N.1    Clardy, J.2
  • 158
    • 34249944904 scopus 로고    scopus 로고
    • Cytotoxic dibromotyrosine-derived metabolites from the sponge Aplysina gerardogreeni
    • Hernández-Guerrero CJ, Zubía E, Ortega MJ, Carballo JL (2007) Cytotoxic dibromotyrosine-derived metabolites from the sponge Aplysina gerardogreeni. Bioorg Med Chem 15: 5275-5282
    • (2007) Bioorg Med Chem , vol.15 , pp. 5275-5282
    • Hernández-Guerrero, C.J.1    Zubía, E.2    Ortega, M.J.3    Carballo, J.L.4
  • 161
    • 0000997713 scopus 로고
    • Brominated tyrosine-derived metabolites from the sponge Ianthella basta
    • Kazlauskas R, Lidgard RO, Murphy PT, Wells RJ (1980) Brominated tyrosine-derived metabolites from the sponge Ianthella basta. Tetrahedron Lett 21: 2277-2280
    • (1980) Tetrahedron Lett , vol.21 , pp. 2277-2280
    • Kazlauskas, R.1    Lidgard, R.O.2    Murphy, P.T.3    Wells, R.J.4
  • 163
    • 0001706777 scopus 로고
    • New bastadins from the sponge Ianthella basta
    • Pordesimo EO, Schmitz FJ (1990) New bastadins from the sponge Ianthella basta. J Org Chem 55: 4704-4709
    • (1990) J Org Chem , vol.55 , pp. 4704-4709
    • Pordesimo, E.O.1    Schmitz, F.J.2
  • 164
    • 0025605642 scopus 로고
    • Cytotoxic metabolites from the sponge Ianthella basta collected in Papua New Guinea
    • Miao S, Andersen RJ, Allen TM (1990) Cytotoxic metabolites from the sponge Ianthella basta collected in Papua New Guinea. J Nat Prod 53: 1441-1446
    • (1990) J Nat Prod , vol.53 , pp. 1441-1446
    • Miao, S.1    Andersen, R.J.2    Allen, T.M.3
  • 165
    • 84970585977 scopus 로고
    • The bastadins revisited: New chemistry from the Australian marine sponge Ianthella basta
    • Butler MS, Lim TK, Capon RJ, Hammond LS (1991) The bastadins revisited: new chemistry from the Australian marine sponge Ianthella basta. Aust J Chem 44: 287-296
    • (1991) Aust J Chem , vol.44 , pp. 287-296
    • Butler, M.S.1    Lim, T.K.2    Capon, R.J.3    Hammond, L.S.4
  • 166
    • 0028304338 scopus 로고
    • The search for inosine 5'-phosphate dehydrogenase (IMPDH) inhibitors from marine sponges. Evaluation of the bastadin alkaloids
    • Jaspars M, Rali T, Laney M, Schatzman RC, Diaz MC, Schmitz FJ, Pordesimo EO, Crews P (1994) The search for inosine 5'-phosphate dehydrogenase (IMPDH) inhibitors from marine sponges. Evaluation of the bastadin alkaloids. Tetrahedron 50: 7367-7374
    • (1994) Tetrahedron , vol.50 , pp. 7367-7374
    • Jaspars, M.1    Rali, T.2    Laney, M.3    Schatzman, R.C.4    Diaz, M.C.5    Schmitz, F.J.6    Pordesimo, E.O.7    Crews, P.8
  • 167
    • 0028314658 scopus 로고
    • Two more bastadins, 16 and 17, from an Indonesian sponge Ianthella basta
    • Park SK, Jurek J, Carney JR, Scheuer PJ (1994) Two more bastadins, 16 and 17, from an Indonesian sponge Ianthella basta. J Nat Prod 57: 407-410
    • (1994) J Nat Prod , vol.57 , pp. 407-410
    • Park, S.K.1    Jurek, J.2    Carney, J.R.3    Scheuer, P.J.4
  • 168
    • 0030462801 scopus 로고    scopus 로고
    • Bastadin 20 and bastadin O-sulfate esters from Ianthella basta: Novel modulators of the Ry1R FKBP12 receptor complex
    • Franklin MA, Penn SG, Lebrilla CB, Lam TH, Pessah IN, Molinski TF (1996) Bastadin 20 and bastadin O-sulfate esters from Ianthella basta: novel modulators of the Ry1R FKBP12 receptor complex. J Nat Prod 59: 1121-1127
    • (1996) J Nat Prod , vol.59 , pp. 1121-1127
    • Franklin, M.A.1    Penn, S.G.2    Lebrilla, C.B.3    Lam, T.H.4    Pessah, I.N.5    Molinski, T.F.6
  • 169
    • 34548542135 scopus 로고    scopus 로고
    • Bastadins, cyclic tetramers of brominated-tyrosine derivatives, selectively inhibit the proliferation of endothelial cells
    • Aoki S, Cho S, Hiramatsu A, Kotoku N, Kobayashi M (2006) Bastadins, cyclic tetramers of brominated-tyrosine derivatives, selectively inhibit the proliferation of endothelial cells. J Nat Med 60: 231-235
    • (2006) J Nat Med , vol.60 , pp. 231-235
    • Aoki, S.1    Cho, S.2    Hiramatsu, A.3    Kotoku, N.4    Kobayashi, M.5
  • 172
    • 0036098849 scopus 로고    scopus 로고
    • Bastadin 21, a novel isobastarane metabolite from the Great Barrier Reef marine sponge Ianthella quadrangulata
    • Coll JC, Kearns PS, Rideout JA, Sankar V (2002) Bastadin 21, a novel isobastarane metabolite from the Great Barrier Reef marine sponge Ianthella quadrangulata. J Nat Prod 65: 753-756
    • (2002) J Nat Prod , vol.65 , pp. 753-756
    • Coll, J.C.1    Kearns, P.S.2    Rideout, J.A.3    Sankar, V.4
  • 174
    • 0027156277 scopus 로고
    • Isolation of a novel bastadin from the temperate marine sponge Ianthella sp
    • Dexter AF, Garson MJ, Hemling ME (1993) Isolation of a novel bastadin from the temperate marine sponge Ianthella sp. J Nat Prod 56: 782-786
    • (1993) J Nat Prod , vol.56 , pp. 782-786
    • Dexter, A.F.1    Garson, M.J.2    Hemling, M.E.3
  • 175
    • 0027462184 scopus 로고
    • A new bastadin from the sponge Psammaplysilla purpurea
    • Carney JR, Scheuer PJ, Kelly-Borges M (1993) A new bastadin from the sponge Psammaplysilla purpurea. J Nat Prod 56: 153-157
    • (1993) J Nat Prod , vol.56 , pp. 153-157
    • Carney, J.R.1    Scheuer, P.J.2    Kelly-Borges, M.3
  • 176
    • 0033025818 scopus 로고    scopus 로고
    • Novel bromine-containing constituents of the sponge Psammaplysilla purpurea
    • Venkateswarlu Y, Venkatesham U, Rao MR (1999) Novel bromine-containing constituents of the sponge Psammaplysilla purpurea. J Nat Prod 62: 893-894
    • (1999) J Nat Prod , vol.62 , pp. 893-894
    • Venkateswarlu, Y.1    Venkatesham, U.2    Rao, M.R.3
  • 178
    • 0029858670 scopus 로고    scopus 로고
    • Isolation and structure of hemibastadinols 1-3 from the Papua New Guinea marine sponge Ianthella basta
    • Pettit GR, Butler MS, Williams MD, Filiatrault MJ, Pettit RK (1996) Isolation and structure of hemibastadinols 1-3 from the Papua New Guinea marine sponge Ianthella basta. J Nat Prod 59: 927-934
    • (1996) J Nat Prod , vol.59 , pp. 927-934
    • Pettit, G.R.1    Butler, M.S.2    Williams, M.D.3    Filiatrault, M.J.4    Pettit, R.K.5
  • 181
    • 0028100737 scopus 로고
    • Novel modulators of skeletal muscle FKBP12/calcium channel complex from Ianthella basta
    • Mack MM, Molinski TF, Buck ED, Pessah IN (1994) Novel modulators of skeletal muscle FKBP12/calcium channel complex from Ianthella basta. J Biol Chem 269: 23236-23249
    • (1994) J Biol Chem , vol.269 , pp. 23236-23249
    • Mack, M.M.1    Molinski, T.F.2    Buck, E.D.3    Pessah, I.N.4
  • 182
    • 0032731158 scopus 로고    scopus 로고
    • Bastadin 10 stabilizes the open conformation of the ryanodine-sensitive Ca2+ channel in an FKBP12-dependent manner
    • Chen L, Molinski TF, Pessah IN (1999) Bastadin 10 stabilizes the open conformation of the ryanodine-sensitive Ca2+ channel in an FKBP12-dependent manner. J Biol Chem 274: 32603-32612
    • (1999) J Biol Chem , vol.274 , pp. 32603-32612
    • Chen, L.1    Molinski, T.F.2    Pessah, I.N.3
  • 183
    • 0034703772 scopus 로고    scopus 로고
    • Chemical defenses of the Caribbean sponges Agelas wiedenmayeri and Agelas conifera
    • Assmann M, Lichte E, Pawlik JR, Koeck M (2000) Chemical defenses of the Caribbean sponges Agelas wiedenmayeri and Agelas conifera. Mar Ecol Prog Ser 207: 255-262
    • (2000) Mar Ecol Prog Ser , vol.207 , pp. 255-262
    • Assmann, M.1    Lichte, E.2    Pawlik, J.R.3    Koeck, M.4
  • 184
    • 1342288742 scopus 로고    scopus 로고
    • Chemical defense of Mediterranean Aplysina cavernicola and Aplysina aerophoba
    • Thoms C, Wolff M, Padmakumar K, Ebel R, Proksch P (2004) Chemical defense of Mediterranean Aplysina cavernicola and Aplysina aerophoba. Z Naturforsch 59c: 113-122
    • (2004) Z Naturforsch , vol.59 c , pp. 113-122
    • Thoms, C.1    Wolff, M.2    Padmakumar, K.3    Ebel, R.4    Proksch, P.5
  • 185
    • 0029095496 scopus 로고
    • Kapakahine B: A cyclic hexapeptide with an a-carboline ring system from the marine sponge Cribrochalina olemda
    • Nakao Y, Yeung BKS, Yoshida WY, Scheuer PJ (1995) Kapakahine B: a cyclic hexapeptide with an a-carboline ring system from the marine sponge Cribrochalina olemda. J Am Chem Soc 117: 8271-8272
    • (1995) J Am Chem Soc , vol.117 , pp. 8271-8272
    • Nakao, Y.1    Yeung, B.K.S.2    Yoshida, W.Y.3    Scheuer, P.J.4
  • 187
    • 0043268087 scopus 로고    scopus 로고
    • More kapakahines from the marine sponge Cribrochalina olemda
    • Nakao Y, Kuo J, Yoshida WY, Kelly M, Scheuer PJ (2003) More kapakahines from the marine sponge Cribrochalina olemda. Org Lett 5: 1387-1390
    • (2003) Org Lett , vol.5 , pp. 1387-1390
    • Nakao, Y.1    Kuo, J.2    Yoshida, W.Y.3    Kelly, M.4    Scheuer, P.J.5
  • 188
    • 0021703445 scopus 로고
    • Bioactive marine metabolites VI. Structure elucidation of discodermin A, and antimicrobial peptide from the marine sponge Discodermia kiiensis
    • Matsunaga S, Fusetani N, Konosu S (1984) Bioactive marine metabolites VI. Structure elucidation of discodermin A, and antimicrobial peptide from the marine sponge Discodermia kiiensis. Tetrahedron Lett 25: 5165-5168
    • (1984) Tetrahedron Lett , vol.25 , pp. 5165-5168
    • Matsunaga, S.1    Fusetani, N.2    Konosu, S.3
  • 189
    • 0021871692 scopus 로고
    • Bioactive marine metabolites IV. Isolation and the amino acid composition of discodermin A, an antimicrobial peptide, from the marine sponge Discodermia kiiensis
    • Matsunaga S, Fusetani N, Konosu S (1985) Bioactive marine metabolites IV. Isolation and the amino acid composition of discodermin A, an antimicrobial peptide, from the marine sponge Discodermia kiiensis. J Nat Prod 48: 236-241
    • (1985) J Nat Prod , vol.48 , pp. 236-241
    • Matsunaga, S.1    Fusetani, N.2    Konosu, S.3
  • 190
    • 0001332133 scopus 로고
    • Bioactive marine metabolites VII. Structures of discodermins B, C, and D, antimicrobial peptides from the marine sponge Discodermia kiiensis
    • Matsunaga S, Fusetani N, Konosu S (1985) Bioactive marine metabolites VII. Structures of discodermins B, C, and D, antimicrobial peptides from the marine sponge Discodermia kiiensis. Tetrahedron Lett 26: 855-856
    • (1985) Tetrahedron Lett , vol.26 , pp. 855-856
    • Matsunaga, S.1    Fusetani, N.2    Konosu, S.3
  • 191
    • 0027939489 scopus 로고
    • Discodermin E, a cytotoxic and antimicrobial tetradecapeptide, from the marine sponge Discodermia kiiensis
    • Ryu G, Matsunaga S, Fusetani N (1994) Discodermin E, a cytotoxic and antimicrobial tetradecapeptide, from the marine sponge Discodermia kiiensis. Tetrahedron Lett 35: 8251-8254
    • (1994) Tetrahedron Lett , vol.35 , pp. 8251-8254
    • Ryu, G.1    Matsunaga, S.2    Fusetani, N.3
  • 192
    • 0028076033 scopus 로고
    • Discodermins F-H, cytotoxic and antimicrobial tetradecapeptides, from the marine sponge Discodermia kiiensis: Structure revision of discodermins A-D
    • Ryu G, Matsunaga S, Fusetani N (1994) Discodermins F-H, cytotoxic and antimicrobial tetradecapeptides, from the marine sponge Discodermia kiiensis: structure revision of discodermins A-D. Tetrahedron 50: 13409-13416
    • (1994) Tetrahedron , vol.50 , pp. 13409-13416
    • Ryu, G.1    Matsunaga, S.2    Fusetani, N.3
  • 193
    • 0028330112 scopus 로고
    • Discobahamins A and B, new peptides from the Bahamian deep water marine sponge Discodermia sp
    • Gunasekera SP, Pomponi SA, McCarthy PJ (1994) Discobahamins A and B, new peptides from the Bahamian deep water marine sponge Discodermia sp. J Nat Prod 57: 79-83
    • (1994) J Nat Prod , vol.57 , pp. 79-83
    • Gunasekera, S.P.1    Pomponi, S.A.2    McCarthy, P.J.3
  • 194
    • 0026519660 scopus 로고
    • Polydiscamide A: A new bioactive depsipeptide from the marine sponge Discodermia sp
    • Gulavita NK, Gunasekera SP, Pomponi SA, Robinson EV (1992) Polydiscamide A: a new bioactive depsipeptide from the marine sponge Discodermia sp. J Org Chem 57: 1767-1772
    • (1992) J Org Chem , vol.57 , pp. 1767-1772
    • Gulavita, N.K.1    Gunasekera, S.P.2    Pomponi, S.A.3    Robinson, E.V.4
  • 195
    • 39049110095 scopus 로고    scopus 로고
    • Polydiscamides B-D from a marine sponge Ircinia sp. as potent human sensory neuron-specific G protein coupled receptor agonists
    • Feng Y, Carroll AR, Pass DM, Archbold JK, Avery VM, Quinn RJ (2008) Polydiscamides B-D from a marine sponge Ircinia sp. as potent human sensory neuron-specific G protein coupled receptor agonists. J Nat Prod 71: 8-11
    • (2008) J Nat Prod , vol.71 , pp. 8-11
    • Feng, Y.1    Carroll, A.R.2    Pass, D.M.3    Archbold, J.K.4    Avery, V.M.5    Quinn, R.J.6
  • 196
    • 0029078819 scopus 로고
    • Halicylindramides A-C, antifungal and cytotoxic depsipeptides from the marine sponge Halichondria cylindrata
    • Li H, Matsunaga S, Fusetani N (1995) Halicylindramides A-C, antifungal and cytotoxic depsipeptides from the marine sponge Halichondria cylindrata. J Med Chem 38: 338-343
    • (1995) J Med Chem , vol.38 , pp. 338-343
    • Li, H.1    Matsunaga, S.2    Fusetani, N.3
  • 197
    • 0030512670 scopus 로고    scopus 로고
    • Halicylindramides D and E, antifungal peptides from the marine sponge Halichondria cylindrata
    • Li H, Matsunaga S, Fusetani N (1996) Halicylindramides D and E, antifungal peptides from the marine sponge Halichondria cylindrata. J Nat Prod 59: 163-166
    • (1996) J Nat Prod , vol.59 , pp. 163-166
    • Li, H.1    Matsunaga, S.2    Fusetani, N.3
  • 198
    • 0035822998 scopus 로고    scopus 로고
    • A diverse family of GPCRs expressed in specific subsets of nociceptive sensory neurons
    • Dong X, Han S, Zylka MJ, Simon MI, Anderson DJ (2001) A diverse family of GPCRs expressed in specific subsets of nociceptive sensory neurons. Cell 106: 619-632
    • (2001) Cell , vol.106 , pp. 619-632
    • Dong, X.1    Han, S.2    Zylka, M.J.3    Simon, M.I.4    Anderson, D.J.5
  • 199
    • 0036179729 scopus 로고    scopus 로고
    • Two faces for an opioid peptide-and more receptors for pain research
    • Simonin F, Kieffer BL (2002) Two faces for an opioid peptide-and more receptors for pain research. Nat Neurosci 5: 185-186
    • (2002) Nat Neurosci , vol.5 , pp. 185-186
    • Simonin, F.1    Kieffer, B.L.2
  • 201
    • 4243562790 scopus 로고
    • Jasplakinolide, a cylcodepsipeptide from the marine sponge, Jaspis sp
    • Crews P, Manes LV, Boehler M (1986) Jasplakinolide, a cylcodepsipeptide from the marine sponge, Jaspis sp. Tetrahedron Lett 27: 2797-2800
    • (1986) Tetrahedron Lett , vol.27 , pp. 2797-2800
    • Crews, P.1    Manes, L.V.2    Boehler, M.3
  • 202
    • 0028241458 scopus 로고
    • Milnamide A, an unusual cytotoxic tripeptide from the marine sponge Auletta cf. constricta
    • Crews P, Farias JJ, Emrich R, Keifer PA (1994) Milnamide A, an unusual cytotoxic tripeptide from the marine sponge Auletta cf. constricta. J Org Chem 59: 2932-2934
    • (1994) J Org Chem , vol.59 , pp. 2932-2934
    • Crews, P.1    Farias, J.J.2    Emrich, R.3    Keifer, P.A.4
  • 203
    • 0028305511 scopus 로고
    • Hemiasterlin and geodiamolide TA; two new cytotoxic peptides from the marine sponge Hemiasterella minor (Kirkpatrick)
    • Talpir R, Benayahu Y, Kashman Y, Pannell L, Schleyer M (1994) Hemiasterlin and geodiamolide TA; two new cytotoxic peptides from the marine sponge Hemiasterella minor (Kirkpatrick). Tetrahedron Lett 35: 4453-4456
    • (1994) Tetrahedron Lett , vol.35 , pp. 4453-4456
    • Talpir, R.1    Benayahu, Y.2    Kashman, Y.3    Pannell, L.4    Schleyer, M.5
  • 204
    • 0023199134 scopus 로고
    • Stereostructures of geodiamolidesAand B, novel cylcodepsipeptides from the marine sponge Geodia sp
    • ChanWR, TintoWF, Manchand PS, Todaro LJ (1987) Stereostructures of geodiamolidesAand B, novel cylcodepsipeptides from the marine sponge Geodia sp. J Org Chem 52: 3091-3093
    • (1987) J Org Chem , vol.52 , pp. 3091-3093
    • Chan, W.R.1    Tinto, W.F.2    Manchand, P.S.3    Todaro, L.J.4
  • 205
    • 0023810585 scopus 로고    scopus 로고
    • New class of antifungal agents: Jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis species
    • Scott VR, Boehme R, Matthews TR (1998) New class of antifungal agents: jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis species. Antimicrob Agents Chemother 32: 1154-1157
    • (1998) Antimicrob Agents Chemother , vol.32 , pp. 1154-1157
    • Scott, V.R.1    Boehme, R.2    Matthews, T.R.3
  • 206
    • 0024596610 scopus 로고
    • Novel marine sponge derived amino acids, 8. conformational analysis of jasplakinolide
    • Inman W, Crews P (1989) Novel marine sponge derived amino acids, 8. conformational analysis of jasplakinolide. J Am Chem Soc 111: 2822-2829
    • (1989) J Am Chem Soc , vol.111 , pp. 2822-2829
    • Inman, W.1    Crews, P.2
  • 207
    • 0033058149 scopus 로고    scopus 로고
    • New jaspamide derivatives from the marine sponge Jaspis splendens collected in Vanuatu
    • Zampella A, Giannini C, Debitus C, Roussakis C, D’Auria MV (1999) New jaspamide derivatives from the marine sponge Jaspis splendens collected in Vanuatu. J Nat Prod 62: 332-334
    • (1999) J Nat Prod , vol.62 , pp. 332-334
    • Zampella, A.1    Giannini, C.2    Debitus, C.3    Roussakis, C.4    D’Auria, M.V.5
  • 211
  • 213
    • 34250860733 scopus 로고    scopus 로고
    • Synthesis and conformational analysis of geodiamolide analogues
    • Marimganti S, Wieneke R, Geyer A, Maier ME (2007) Synthesis and conformational analysis of geodiamolide analogues. Eur J Org Chem 2007: 2779-2790
    • (2007) Eur J Org Chem , vol.2007 , pp. 2779-2790
    • Marimganti, S.1    Wieneke, R.2    Geyer, A.3    Maier, M.E.4
  • 214
    • 0025105061 scopus 로고
    • Geodiamolides C to F, new cytotoxic cyclodepsipeptides from the marine sponge Pseudaxinyssa sp
    • de Silva ED, Andersen RJ, Allen TM (1990) Geodiamolides C to F, new cytotoxic cyclodepsipeptides from the marine sponge Pseudaxinyssa sp. Tetrahedron Lett 31: 489-492
    • (1990) Tetrahedron Lett , vol.31 , pp. 489-492
    • de Silva, E.D.1    Andersen, R.J.2    Allen, T.M.3
  • 215
  • 216
    • 0032580336 scopus 로고    scopus 로고
    • Geodiamolides H and I, further cyclodepsipeptides from the marine sponge Geodia sp
    • Tinto WF, Lough AJ, McLean S, Reynolds WF, Yu M, Chan WR (1998) Geodiamolides H and I, further cyclodepsipeptides from the marine sponge Geodia sp. Tetrahedron 54: 4451-4458
    • (1998) Tetrahedron , vol.54 , pp. 4451-4458
    • Tinto, W.F.1    Lough, A.J.2    McLean, S.3    Reynolds, W.F.4    Yu, M.5    Chan, W.R.6
  • 217
    • 0028924635 scopus 로고
    • Neosiphoniamolide A, a novel cyclodepsipeptide with antifungal activity from the marine sponge Neosiphonia superstes
    • D’Auria MV, Paloma LG, Minale L, Zampella A, Debitus C, Perez J (1995) Neosiphoniamolide A, a novel cyclodepsipeptide with antifungal activity from the marine sponge Neosiphonia superstes. J Nat Prod 58: 121-123
    • (1995) J Nat Prod , vol.58 , pp. 121-123
    • D’Auria, M.V.1    Paloma, L.G.2    Minale, L.3    Zampella, A.4    Debitus, C.5    Perez, J.6
  • 218
    • 0032859532 scopus 로고    scopus 로고
    • New geodiamolides from the sponge Cymbastela sp. collected in Papua New Guinea
    • Coleman JE, van Soest R, Andersen RJ (1999) New geodiamolides from the sponge Cymbastela sp. collected in Papua New Guinea. J Nat Prod 62: 1137-1141
    • (1999) J Nat Prod , vol.62 , pp. 1137-1141
    • Coleman, J.E.1    van Soest, R.2    Andersen, R.J.3
  • 219
    • 0028971654 scopus 로고
    • Chondramides A-D, new antifungal and cytostatic depsipeptides from Chondromyces crocatus (Myxobacteria) Production, physico-chemical and biological properties
    • Kunze B, Jansen R, Sasse F, Hoefle G, Reichenbach H (1995) Chondramides A-D, new antifungal and cytostatic depsipeptides from Chondromyces crocatus (Myxobacteria) Production, physico-chemical and biological properties. J Antibiot 48: 1262-1266
    • (1995) J Antibiot , vol.48 , pp. 1262-1266
    • Kunze, B.1    Jansen, R.2    Sasse, F.3    Hoefle, G.4    Reichenbach, H.5
  • 222
    • 0031060389 scopus 로고    scopus 로고
    • Cytotoxic peptides hemiasterlin, hemiasterlin A and hemiasterlin B induce mitotic arrest and abnormal spindle formation
    • Anderson HJ, Coleman JE, Andersen RJ, Roberge M (1997) Cytotoxic peptides hemiasterlin, hemiasterlin A and hemiasterlin B induce mitotic arrest and abnormal spindle formation. Cancer Chemother Pharmacol 39: 223-226
    • (1997) Cancer Chemother Pharmacol , vol.39 , pp. 223-226
    • Anderson, H.J.1    Coleman, J.E.2    Andersen, R.J.3    Roberge, M.4
  • 230
    • 0028117690 scopus 로고
    • Arenastatin A, a potent cytotoxic depsipeptide from the Okinawan marine sponge Dysidea arenaria
    • Kobayashi M, Aoki S, Ohyabu N, Kurosu M, Wang W, Kitagawa I (1994) Arenastatin A, a potent cytotoxic depsipeptide from the Okinawan marine sponge Dysidea arenaria. Tetrahedron Lett 35: 7969-7972
    • (1994) Tetrahedron Lett , vol.35 , pp. 7969-7972
    • Kobayashi, M.1    Aoki, S.2    Ohyabu, N.3    Kurosu, M.4    Wang, W.5    Kitagawa, I.6
  • 231
    • 0028114331 scopus 로고
    • The absolute stereostructure of arenastatin A, a potent cytotoxic depsipeptide from the Okinawan marine sponge Dysidea arenaria
    • Kobayashi M, Kurosu M, Ohyabu N, Wang W, Fujii S, Kitagawa I (1994) The absolute stereostructure of arenastatin A, a potent cytotoxic depsipeptide from the Okinawan marine sponge Dysidea arenaria. Chem Pharm Bull 42: 2196-2198
    • (1994) Chem Pharm Bull , vol.42 , pp. 2196-2198
    • Kobayashi, M.1    Kurosu, M.2    Ohyabu, N.3    Wang, W.4    Fujii, S.5    Kitagawa, I.6
  • 232
    • 0027985510 scopus 로고
    • A total synthesis of arenastatin A, an extremely potent cytotoxic depsipeptide, from the Okinawan marine sponge Dysidea arenaria
    • Kobayashi M, Kurosu M, Wang W, Kitagawa I (1994) A total synthesis of arenastatin A, an extremely potent cytotoxic depsipeptide, from the Okinawan marine sponge Dysidea arenaria. Chem Pharm Bull 42: 2394-2396
    • (1994) Chem Pharm Bull , vol.42 , pp. 2394-2396
    • Kobayashi, M.1    Kurosu, M.2    Wang, W.3    Kitagawa, I.4
  • 234
    • 4344670607 scopus 로고    scopus 로고
    • Dysinosins B-D, inhibitors of factor VIIa and thrombin from the Australian sponge Lamellodysidea chlorea
    • Carroll AR, Buchanan MS, Edser A, Hyde E, Simpson M, Quinn RJ (2004) Dysinosins B-D, inhibitors of factor VIIa and thrombin from the Australian sponge Lamellodysidea chlorea. J Nat Prod 67: 1291-1294
    • (2004) J Nat Prod , vol.67 , pp. 1291-1294
    • Carroll, A.R.1    Buchanan, M.S.2    Edser, A.3    Hyde, E.4    Simpson, M.5    Quinn, R.J.6
  • 235
    • 0033520230 scopus 로고    scopus 로고
    • Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Okita Y, Matsuda H, Okino T, Murakami M (1999) Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa. Tetrahedron 55: 10971-10988
    • (1999) Tetrahedron , vol.55 , pp. 10971-10988
    • Ishida, K.1    Okita, Y.2    Matsuda, H.3    Okino, T.4    Murakami, M.5
  • 236
    • 0030580449 scopus 로고    scopus 로고
    • Aeruginosins 102-A and B, new thrombin inhibitors from the cyanobacterium Microcystis viridis (NIES-102)
    • Matsuda H, Okino T, Murakami M, Yamaguchi K (1996) Aeruginosins 102-A and B, new thrombin inhibitors from the cyanobacterium Microcystis viridis (NIES-102). Tetrahedron 52: 14501-14506
    • (1996) Tetrahedron , vol.52 , pp. 14501-14506
    • Matsuda, H.1    Okino, T.2    Murakami, M.3    Yamaguchi, K.4
  • 237
    • 0028957349 scopus 로고
    • Aeruginosins 98-A and B, trypsin inhibitors from the blue-green alga Microcystis aeruginosa (NIES-98)
    • Murakami M, Ishida K, Okino T, Okita Y, Matsuda H, Yamaguchi K (1995) Aeruginosins 98-A and B, trypsin inhibitors from the blue-green alga Microcystis aeruginosa (NIES-98). Tetrahedron Lett 36: 2785-2788
    • (1995) Tetrahedron Lett , vol.36 , pp. 2785-2788
    • Murakami, M.1    Ishida, K.2    Okino, T.3    Okita, Y.4    Matsuda, H.5    Yamaguchi, K.6
  • 240
    • 0028235881 scopus 로고
    • Antineoplastic agents. 277. Isolation and structure of phakellistatin 3 and isophakellistatin 3 from a Republic of Comoros marine sponge
    • Pettit GR, Tan R, Herald DL, Cerny RL, Williams MD (1994) Antineoplastic agents. 277. Isolation and structure of phakellistatin 3 and isophakellistatin 3 from a Republic of Comoros marine sponge. J Org Chem 59: 1593-1595
    • (1994) J Org Chem , vol.59 , pp. 1593-1595
    • Pettit, G.R.1    Tan, R.2    Herald, D.L.3    Cerny, R.L.4    Williams, M.D.5
  • 242
    • 0027985318 scopus 로고
    • Antineoplastic agents 323. Isolation and structure of phakellistatin 6 from a Chuuk Archipelago marine sponge
    • Pettit GR, Xu J, Cichacz ZA, Williams MD, Chapuis J, Cerny RL (1994) Antineoplastic agents 323. Isolation and structure of phakellistatin 6 from a Chuuk Archipelago marine sponge. Bioorg Med Chem Lett 4: 2677-2682
    • (1994) Bioorg Med Chem Lett , vol.4 , pp. 2677-2682
    • Pettit, G.R.1    Xu, J.2    Cichacz, Z.A.3    Williams, M.D.4    Chapuis, J.5    Cerny, R.L.6
  • 243
    • 0029032630 scopus 로고
    • Isolation and structure of the human cancer cell growth inhibitory cyclic decapeptides phakellistatins 7, 8 and 9
    • Pettit GR, Xu J, Dorsaz A, Williams MD, Boyd MR, Cerny RL (1995) Isolation and structure of the human cancer cell growth inhibitory cyclic decapeptides phakellistatins 7, 8 and 9. Bioorg Med Chem Lett 5: 1339-1344
    • (1995) Bioorg Med Chem Lett , vol.5 , pp. 1339-1344
    • Pettit, G.R.1    Xu, J.2    Dorsaz, A.3    Williams, M.D.4    Boyd, M.R.5    Cerny, R.L.6
  • 245
    • 0037293855 scopus 로고    scopus 로고
    • Antineoplastic agents 390. Isolation and structure of phakellistatin 12 from a Chuuk Archipelago marine sponge
    • Pettit GR, Tan R (2003) Antineoplastic agents 390. Isolation and structure of phakellistatin 12 from a Chuuk Archipelago marine sponge. Bioorg Med Chem Lett 13: 685-688
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 685-688
    • Pettit, G.R.1    Tan, R.2
  • 246
    • 12244287902 scopus 로고    scopus 로고
    • Isolation and structure of the cytotoxic cycloheptapeptide phakellistatin 13
    • Li W, Yi Y, Wu H, Xu Q, Tang H, Zhou D, Lin H, Wang Z (2003) Isolation and structure of the cytotoxic cycloheptapeptide phakellistatin 13. J Nat Prod 66: 146-148
    • (2003) J Nat Prod , vol.66 , pp. 146-148
    • Li, W.1    Yi, Y.2    Wu, H.3    Xu, Q.4    Tang, H.5    Zhou, D.6    Lin, H.7    Wang, Z.8
  • 247
    • 12944265406 scopus 로고    scopus 로고
    • Isolation and structure of phakellistatin 14 from the Western Pacific marine sponge Phakellia sp
    • Pettit GR, Tan R (2005) Isolation and structure of phakellistatin 14 from the Western Pacific marine sponge Phakellia sp. J Nat Prod 68: 60-63
    • (2005) J Nat Prod , vol.68 , pp. 60-63
    • Pettit, G.R.1    Tan, R.2
  • 248
    • 0037195718 scopus 로고    scopus 로고
    • Two distinct conformers of the cyclic heptapeptide phakellistatin 2 isolated from the Fijian marine sponge Stylotella aurantium
    • Tabudravu JN, Jaspars M, Morris LA, Kettenes-van den Bosch JJ, Smith N (2002) Two distinct conformers of the cyclic heptapeptide phakellistatin 2 isolated from the Fijian marine sponge Stylotella aurantium. J Org Chem 67: 8593-8601
    • (2002) J Org Chem , vol.67 , pp. 8593-8601
    • Tabudravu, J.N.1    Jaspars, M.2    Morris, L.A.3    Kettenes-van den Bosch, J.J.4    Smith, N.5
  • 249
    • 0027461341 scopus 로고
    • Hymenamides A and B, new proline-rich cyclic heptapeptides from the Okinawan marine sponge Hymeniacidon sp
    • Kobayashi J, Tsuda M, Nakamura T, Mikami Y, Shigemori H (1993) Hymenamides A and B, new proline-rich cyclic heptapeptides from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 49: 2391-2402
    • (1993) Tetrahedron , vol.49 , pp. 2391-2402
    • Kobayashi, J.1    Tsuda, M.2    Nakamura, T.3    Mikami, Y.4    Shigemori, H.5
  • 250
    • 0027182909 scopus 로고
    • Hymenamides C-E, new cyclic heptapeptides with two proline residues from the Okinawan marine sponge Hymeniacidon sp
    • Tsuda M, Shigemori H, Mikami Y, Kobayashi J (1993) Hymenamides C-E, new cyclic heptapeptides with two proline residues from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 49: 6785-6796
    • (1993) Tetrahedron , vol.49 , pp. 6785-6796
    • Tsuda, M.1    Shigemori, H.2    Mikami, Y.3    Kobayashi, J.4
  • 251
    • 0029967644 scopus 로고    scopus 로고
    • Hymenamide F, new cyclic heptapeptide from marine sponge Hymeniacidon sp
    • Kobayashi J, Nakamura T, Tsuda M (1996) Hymenamide F, new cyclic heptapeptide from marine sponge Hymeniacidon sp. Tetrahedron 52: 6355-6360
    • (1996) Tetrahedron , vol.52 , pp. 6355-6360
    • Kobayashi, J.1    Nakamura, T.2    Tsuda, M.3
  • 252
    • 0028222655 scopus 로고
    • Hymenamides G, H, J, and K, four new cyclid octapeptides from the Okinawan marine sponge Hymeniacidon sp
    • Tsuda M, Sasaki T, Kobayashi J (1994) Hymenamides G, H, J, and K, four new cyclid octapeptides from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 50: 4667-4680
    • (1994) Tetrahedron , vol.50 , pp. 4667-4680
    • Tsuda, M.1    Sasaki, T.2    Kobayashi, J.3
  • 254
    • 0029977986 scopus 로고    scopus 로고
    • Immunosuppressive activity of hymenistatin I
    • Cebrat M, Wieczorek Z, Siemion IZ (1996) Immunosuppressive activity of hymenistatin I. Peptides 17: 191-196
    • (1996) Peptides , vol.17 , pp. 191-196
    • Cebrat, M.1    Wieczorek, Z.2    Siemion, I.Z.3
  • 255
    • 0028297115 scopus 로고
    • Antineoplastic agents. 278. Isolation and structure of axinastatins 2 and 3 from a Western Caroline Island marine sponge
    • Pettit GR, Gao F, Cerny RL, Doubek DL, Tackett LP, Schmidt JM, Chapuis J (1994) Antineoplastic agents. 278. Isolation and structure of axinastatins 2 and 3 from a Western Caroline Island marine sponge. J Med Chem 37: 1165-1168
    • (1994) J Med Chem , vol.37 , pp. 1165-1168
    • Pettit, G.R.1    Gao, F.2    Cerny, R.L.3    Doubek, D.L.4    Tackett, L.P.5    Schmidt, J.M.6    Chapuis, J.7
  • 256
    • 0028595894 scopus 로고
    • Isolation and structure of axinastatin 5 from a Republic of Comoros marine sponge
    • Pettit GR, Gao F, Schmidt JM, Chapuis J (1994) Isolation and structure of axinastatin 5 from a Republic of Comoros marine sponge. Bioorg Med Chem Lett 4: 2935-2940
    • (1994) Bioorg Med Chem Lett , vol.4 , pp. 2935-2940
    • Pettit, G.R.1    Gao, F.2    Schmidt, J.M.3    Chapuis, J.4
  • 257
    • 2842581685 scopus 로고    scopus 로고
    • Axinellins A and B: New proline-containing antiproliferative cyclopeptides from the Vanuatu sponge Axinella carteri
    • Randazzo A, Dal Piaz F, Orrù S, Debitus C, Roussakis C, Pucci P, Gomez-Paloma L (1998) Axinellins A and B: new proline-containing antiproliferative cyclopeptides from the Vanuatu sponge Axinella carteri. Eur J Org Chem 1998: 2659-2665
    • (1998) Eur J Org Chem , vol.1998 , pp. 2659-2665
    • Randazzo, A.1    Dal Piaz, F.2    Orrù, S.3    Debitus, C.4    Roussakis, C.5    Pucci, P.6    Gomez-Paloma, L.7
  • 258
    • 0037163273 scopus 로고    scopus 로고
    • Axinellin C, a proline-rich cyclic octapeptide isolated from the Fijian marine sponge Stylotella aurantium
    • Tabudravu JN, Morris LA, Kettenes-van den Bosch JJ, Jaspars M (2002) Axinellin C, a proline-rich cyclic octapeptide isolated from the Fijian marine sponge Stylotella aurantium. Tetrahedron 58: 7863-7868
    • (2002) Tetrahedron , vol.58 , pp. 7863-7868
    • Tabudravu, J.N.1    Morris, L.A.2    Kettenes-van den Bosch, J.J.3    Jaspars, M.4
  • 259
    • 34548085465 scopus 로고    scopus 로고
    • Stylissamides A-D-new proline-containing cyclic heptapeptides from the marine sponge Stylissa caribica
    • Schmidt G, Grube A, Koeck M (2007) Stylissamides A-D-new proline-containing cyclic heptapeptides from the marine sponge Stylissa caribica. Eur J Org Chem 2007: 4103-4110
    • (2007) Eur J Org Chem , vol.2007 , pp. 4103-4110
    • Schmidt, G.1    Grube, A.2    Koeck, M.3
  • 260
    • 33846446696 scopus 로고    scopus 로고
    • Cyclic heptapeptides from the Jamaican sponge Stylissa caribica
    • Mohammed R, Peng J, Kelly M, Hamann MT (2006) Cyclic heptapeptides from the Jamaican sponge Stylissa caribica. J Nat Prod 69: 1739-1744
    • (2006) J Nat Prod , vol.69 , pp. 1739-1744
    • Mohammed, R.1    Peng, J.2    Kelly, M.3    Hamann, M.T.4
  • 261
    • 17544379500 scopus 로고    scopus 로고
    • Haligramides A and B, two new cytotoxic hexapeptides from the marine sponge Haliclona nigra
    • Rashid MA, Gustafson KR, Boswell JL, Boyd MR (2000) Haligramides A and B, two new cytotoxic hexapeptides from the marine sponge Haliclona nigra. J Nat Prod 63: 956-959
    • (2000) J Nat Prod , vol.63 , pp. 956-959
    • Rashid, M.A.1    Gustafson, K.R.2    Boswell, J.L.3    Boyd, M.R.4
  • 262
    • 0035823849 scopus 로고    scopus 로고
    • Halipeptins A and B: Two novel potent anti-inflammatory cyclic depsipeptides from the Vanuatu marine sponge Haliclona sp
    • Randazzo A, Bifulco G, Giannini C, Bucci M, Debitus C, Cirino G, Gomez-Paloma L (2001) Halipeptins A and B: two novel potent anti-inflammatory cyclic depsipeptides from the Vanuatu marine sponge Haliclona sp. J Am Chem Soc 123: 10870-10876
    • (2001) J Am Chem Soc , vol.123 , pp. 10870-10876
    • Randazzo, A.1    Bifulco, G.2    Giannini, C.3    Bucci, M.4    Debitus, C.5    Cirino, G.6    Gomez-Paloma, L.7
  • 264
  • 265
    • 70349484638 scopus 로고    scopus 로고
    • Isolation and structural elucidation of euryjanicins B-D, proline-containing cycloheptapeptides from the Caribbean marine sponge Prosuberites laughlini
    • Vera B, Vicente J, Rodríguez AD (2009) Isolation and structural elucidation of euryjanicins B-D, proline-containing cycloheptapeptides from the Caribbean marine sponge Prosuberites laughlini. J Nat Prod 72: 1555-1562
    • (2009) J Nat Prod , vol.72 , pp. 1555-1562
    • Vera, B.1    Vicente, J.2    Rodríguez, A.D.3
  • 266
    • 0024598229 scopus 로고
    • Theonellamide F. A novel antifungal bicyclic peptide from a marine sponge Theonella sp
    • Matsunaga S, Fusetani N, Hashimoto K, Waelchli M (1989) Theonellamide F. A novel antifungal bicyclic peptide from a marine sponge Theonella sp. J Am Chem Soc 111: 2582-2588
    • (1989) J Am Chem Soc , vol.111 , pp. 2582-2588
    • Matsunaga, S.1    Fusetani, N.2    Hashimoto, K.3    Waelchli, M.4
  • 267
    • 0028945772 scopus 로고
    • Theonellamides A-E, cytotoxic bicyclic peptides, from a marine sponge Theonella sp
    • Matsunaga S, Fusetani N (1995) Theonellamides A-E, cytotoxic bicyclic peptides, from a marine sponge Theonella sp. J Org Chem 60: 1177-1181
    • (1995) J Org Chem , vol.60 , pp. 1177-1181
    • Matsunaga, S.1    Fusetani, N.2
  • 268
    • 0028118767 scopus 로고
    • Polytheonamides, unprecedented highly cytotoxic polypeptides, from the marine sponge Theonella swinhoei 1. Isolation and component amino acids
    • Hamada T, Sugawara T, Matsunaga S, Fusetani N (1994) Polytheonamides, unprecedented highly cytotoxic polypeptides, from the marine sponge Theonella swinhoei 1. Isolation and component amino acids. Tetrahedron Lett 35: 719-720
    • (1994) Tetrahedron Lett , vol.35 , pp. 719-720
    • Hamada, T.1    Sugawara, T.2    Matsunaga, S.3    Fusetani, N.4
  • 269
    • 11844280935 scopus 로고    scopus 로고
    • Polytheonamides A and B, highly cytotoxic, linear polypeptides with unprecedented structural features, from the marine sponge, Theonella swinhoei
    • Hamada T, Matsunaga S, Yano G, Fusetani N (2005) Polytheonamides A and B, highly cytotoxic, linear polypeptides with unprecedented structural features, from the marine sponge, Theonella swinhoei. J Am Chem Soc 127: 110-118
    • (2005) J Am Chem Soc , vol.127 , pp. 110-118
    • Hamada, T.1    Matsunaga, S.2    Yano, G.3    Fusetani, N.4
  • 270
    • 0024992889 scopus 로고
    • Cyclotheonamides, potent thrombin inhibitors, from a marine sponge Theonella sp
    • Fusetani N, Matsunaga S (1990) Cyclotheonamides, potent thrombin inhibitors, from a marine sponge Theonella sp. J Am Chem Soc 112: 7053-7054
    • (1990) J Am Chem Soc , vol.112 , pp. 7053-7054
    • Fusetani, N.1    Matsunaga, S.2
  • 271
    • 0029130165 scopus 로고
    • Three more cyclotheonamides, C, D, and E, potent thrombin inhibitors from the marine sponge Theonella swinhoei
    • Nakao Y, Matsunaga S, Fusetani N (1995) Three more cyclotheonamides, C, D, and E, potent thrombin inhibitors from the marine sponge Theonella swinhoei. Bioorg Med Chem 3: 1115-1122
    • (1995) Bioorg Med Chem , vol.3 , pp. 1115-1122
    • Nakao, Y.1    Matsunaga, S.2    Fusetani, N.3
  • 272
    • 0031799026 scopus 로고    scopus 로고
    • Cyclotheonamides E2 and E3, new potent serine protease inhibitors fromthemarine sponge of the genus Theonella
    • Nakao Y, Oku N, Matsunaga S, Fusetani N (1998) Cyclotheonamides E2 and E3, new potent serine protease inhibitors fromthemarine sponge of the genus Theonella. JNat Prod 61: 667-670
    • (1998) JNat Prod , vol.61 , pp. 667-670
    • Nakao, Y.1    Oku, N.2    Matsunaga, S.3    Fusetani, N.4
  • 273
    • 0036198756 scopus 로고    scopus 로고
    • Cyclotheonamides E4 and E5, new potent tryptase inhibitors from an Ircinia species of sponge
    • Murakami Y, Takei M, Shindo K, Kitazume C, Tanaka J, Higa T, Fukamachi H (2002) Cyclotheonamides E4 and E5, new potent tryptase inhibitors from an Ircinia species of sponge. J Nat Prod 65: 259-261
    • (2002) J Nat Prod , vol.65 , pp. 259-261
    • Murakami, Y.1    Takei, M.2    Shindo, K.3    Kitazume, C.4    Tanaka, J.5    Higa, T.6    Fukamachi, H.7
  • 274
    • 0033599492 scopus 로고    scopus 로고
    • Pseudotheonamides, serine protease inhibitors from the marine sponge Theonella swinhoei
    • Nakao Y, Masuda A, Matsunaga S, Fusetani N (1999) Pseudotheonamides, serine protease inhibitors from the marine sponge Theonella swinhoei. J Am Chem Soc 121: 2425-2431
    • (1999) J Am Chem Soc , vol.121 , pp. 2425-2431
    • Nakao, Y.1    Masuda, A.2    Matsunaga, S.3    Fusetani, N.4
  • 275
    • 0022485332 scopus 로고
    • Structure of theonellapeptolide Id, a new bioactive peptolide from an Okinawan marine sponge, Theonella sp
    • Kitagawa I, Kobayashi M, Lee NK, Shibuya H, Kawata Y, Sakiyama F (1986) Structure of theonellapeptolide Id, a new bioactive peptolide from an Okinawan marine sponge, Theonella sp. Chem Pharm Bull 34: 2664-2667
    • (1986) Chem Pharm Bull , vol.34 , pp. 2664-2667
    • Kitagawa, I.1    Kobayashi, M.2    Lee, N.K.3    Shibuya, H.4    Kawata, Y.5    Sakiyama, F.6
  • 276
    • 0023337957 scopus 로고
    • Structure of theonellapeptolide Ie, a new tridecapeptide lactone from an Okinawan marine sponge, Theonella sp. (Theonellidae)
    • Kitagawa I, Lee NK, Kobayashi M, Shibuya H (1987) Structure of theonellapeptolide Ie, a new tridecapeptide lactone from an Okinawan marine sponge, Theonella sp. (Theonellidae). Chem Pharm Bull 35: 2129-2132
    • (1987) Chem Pharm Bull , vol.35 , pp. 2129-2132
    • Kitagawa, I.1    Lee, N.K.2    Kobayashi, M.3    Shibuya, H.4
  • 277
    • 0026065255 scopus 로고
    • Marine natural products. XXV. Biologically active tridecapeptide lactones from the Okinawan marine sponge Theonella swinhoei (Theonellidae) (1). Structure of theonellapeptolide Id
    • Kitagawa I, Lee NK, Kobayashi M, Shibuya H (1991) Marine natural products. XXV. Biologically active tridecapeptide lactones from the Okinawan marine sponge Theonella swinhoei (Theonellidae) (1). Structure of theonellapeptolide Id. Tetrahedron 47: 2169-2180
    • (1991) Tetrahedron , vol.47 , pp. 2169-2180
    • Kitagawa, I.1    Lee, N.K.2    Kobayashi, M.3    Shibuya, H.4
  • 278
    • 0025893070 scopus 로고
    • Marine natural products. XXVL. Biologically active tridecapeptide lactones from the Okinawan marine sponge Theonella swinhoei (Theonellidae). (2). Structures of theonellapeptolides Ia, Ib, Ic, and Ie
    • Kobayashi M, Lee NK, Shibuya H, Momose T, Kitagawa I (1991) Marine natural products. XXVL. Biologically active tridecapeptide lactones from the Okinawan marine sponge Theonella swinhoei (Theonellidae). (2). Structures of theonellapeptolides Ia, Ib, Ic, and Ie. Chem Pharm Bull 39: 1177-1184
    • (1991) Chem Pharm Bull , vol.39 , pp. 1177-1184
    • Kobayashi, M.1    Lee, N.K.2    Shibuya, H.3    Momose, T.4    Kitagawa, I.5
  • 279
    • 0033588213 scopus 로고    scopus 로고
    • Two theonellapeptolide congeners from marine sponge Theonella sp
    • Tsuda M, Shimbo K, Kubota T, Mikami Y, Kobayashi J (1999) Two theonellapeptolide congeners from marine sponge Theonella sp. Tetrahedron 55: 10305-10314
    • (1999) Tetrahedron , vol.55 , pp. 10305-10314
    • Tsuda, M.1    Shimbo, K.2    Kubota, T.3    Mikami, Y.4    Kobayashi, J.5
  • 280
    • 0028059367 scopus 로고
    • Marine natural products. XXXIII. Theonellapeptolide IId, a new tridecapeptide lactone from the Okinawan marine sponge Theonella swinhoei
    • Kobayashi M, Kanzaki K, Katayama S, Ohashi K, Okada H, Ikegami S, Kitagawa I (1994) Marine natural products. XXXIII. Theonellapeptolide IId, a new tridecapeptide lactone from the Okinawan marine sponge Theonella swinhoei. Chem Pharm Bull 42: 1410-1415
    • (1994) Chem Pharm Bull , vol.42 , pp. 1410-1415
    • Kobayashi, M.1    Kanzaki, K.2    Katayama, S.3    Ohashi, K.4    Okada, H.5    Ikegami, S.6    Kitagawa, I.7
  • 282
    • 0033575428 scopus 로고    scopus 로고
    • Barangamide A, a new cyclic peptide from the Indonesian sponge Theonella swinhoei
    • Roy MC, Ohtani II, Tanaka J, Higa T, Satari R (1999) Barangamide A, a new cyclic peptide from the Indonesian sponge Theonella swinhoei. Tetrahedron Lett 40: 5373-5376
    • (1999) Tetrahedron Lett , vol.40 , pp. 5373-5376
    • Roy, M.C.1    Ohtani, I.I.2    Tanaka, J.3    Higa, T.4    Satari, R.5
  • 283
    • 0022531490 scopus 로고
    • Theonellamine B, a novel peptidal Na+, K+-ATPase inhibitor from an Okinawan marine sponge of the genus Theonella
    • Nakamura H, Kobayashi J, Nakamura Y, Ohizumi Y, Kondo T, Hirata Y (1986) Theonellamine B, a novel peptidal Na+, K+-ATPase inhibitor from an Okinawan marine sponge of the genus Theonella. Tetrahedron Lett 27: 4319-4322
    • (1986) Tetrahedron Lett , vol.27 , pp. 4319-4322
    • Nakamura, H.1    Kobayashi, J.2    Nakamura, Y.3    Ohizumi, Y.4    Kondo, T.5    Hirata, Y.6
  • 284
    • 0031820647 scopus 로고    scopus 로고
    • Theonellapeptolide IIIe, a new cyclic peptolide from the New Zealand deep water sponge Lamellomorpha strongylata
    • Li S, Dumdei EJ, Blunt JW, Munro MHG, Robinson WT, Pannell LK (1998) Theonellapeptolide IIIe, a new cyclic peptolide from the New Zealand deep water sponge Lamellomorpha strongylata. J Nat Prod 61: 724-728
    • (1998) J Nat Prod , vol.61 , pp. 724-728
    • Li, S.1    Dumdei, E.J.2    Blunt, J.W.3    Munro, M.H.G.4    Robinson, W.T.5    Pannell, L.K.6
  • 286
    • 37249041669 scopus 로고    scopus 로고
    • Mirabamides A-D, depsipeptides from the sponge Siliquariaspongia mirabilis that inhibit HIV-1 fusion
    • Plaza A, Gustchina E, Baker HL, Kelly M, Bewley CA (2007) Mirabamides A-D, depsipeptides from the sponge Siliquariaspongia mirabilis that inhibit HIV-1 fusion. J Nat Prod 70: 1753-1760
    • (2007) J Nat Prod , vol.70 , pp. 1753-1760
    • Plaza, A.1    Gustchina, E.2    Baker, H.L.3    Kelly, M.4    Bewley, C.A.5
  • 288
    • 60849089353 scopus 로고    scopus 로고
    • Celebesides A-C and theonpapuamides B-D, depsipeptides from an Indonesian sponge that inhibit HIV-1 entry
    • Plaza A, Bifulco G, Keffer JL, Lloyd JR, Baker HL, Bewley CA (2009) Celebesides A-C and theonpapuamides B-D, depsipeptides from an Indonesian sponge that inhibit HIV-1 entry. J Org Chem 74: 504-512
    • (2009) J Org Chem , vol.74 , pp. 504-512
    • Plaza, A.1    Bifulco, G.2    Keffer, J.L.3    Lloyd, J.R.4    Baker, H.L.5    Bewley, C.A.6
  • 289
    • 0028088016 scopus 로고
    • Isolation and structure elucidation of perthamide B, a novel peptide from the sponge Theonella sp
    • Gulavita NK, Pomponi SA, Wright AE, Yarwood D, Silis MA (1994) Isolation and structure elucidation of perthamide B, a novel peptide from the sponge Theonella sp. Tetrahedron Lett 35: 6815-6818
    • (1994) Tetrahedron Lett , vol.35 , pp. 6815-6818
    • Gulavita, N.K.1    Pomponi, S.A.2    Wright, A.E.3    Yarwood, D.4    Silis, M.A.5
  • 291
    • 0028128310 scopus 로고
    • Microsclerodermins A and B. Antifungal cyclic peptides from the lithistid sponge Microscleroderma sp
    • Bewley CA, Debitus C, Faulkner DJ (1994) Microsclerodermins A and B. Antifungal cyclic peptides from the lithistid sponge Microscleroderma sp. J Am Chem Soc 116: 7631-7636
    • (1994) J Am Chem Soc , vol.116 , pp. 7631-7636
    • Bewley, C.A.1    Debitus, C.2    Faulkner, D.J.3
  • 292
    • 0032568379 scopus 로고    scopus 로고
    • Microsclerodermins C-E, antifungal cyclic peptides from the lithistid marine sponges Theonella sp. and Microscleroderma sp
    • Schmidt EW, Faulkner DJ (1998) Microsclerodermins C-E, antifungal cyclic peptides from the lithistid marine sponges Theonella sp. and Microscleroderma sp. Tetrahedron 54: 3043-3056
    • (1998) Tetrahedron , vol.54 , pp. 3043-3056
    • Schmidt, E.W.1    Faulkner, D.J.2
  • 293
    • 0034595622 scopus 로고    scopus 로고
    • Microsclerodermins F-I, antitumor and antifungal cyclic peptides from the lithistid sponge Microscleroderma sp
    • Qureshi A, Colin PL, Faulkner DJ (2000) Microsclerodermins F-I, antitumor and antifungal cyclic peptides from the lithistid sponge Microscleroderma sp. Tetrahedron 56: 3679-3685
    • (2000) Tetrahedron , vol.56 , pp. 3679-3685
    • Qureshi, A.1    Colin, P.L.2    Faulkner, D.J.3
  • 295
    • 23944442801 scopus 로고    scopus 로고
    • Koshikamide A2, a cytotoxic linear undecapeptide isolated from a marine sponge of Theonella sp
    • Araki T, Matsunaga S, Fusetani N (2005) Koshikamide A2, a cytotoxic linear undecapeptide isolated from a marine sponge of Theonella sp. Biosci Biotechnol Biochem 69: 1318-1322
    • (2005) Biosci Biotechnol Biochem , vol.69 , pp. 1318-1322
    • Araki, T.1    Matsunaga, S.2    Fusetani, N.3
  • 299
    • 0026669012 scopus 로고
    • Keramamide F, a new thiazole-containing peptide from the Okinawan marine sponge Theonella sp
    • Itagaki F, Shigemori H, Ishibashi M, Nakamura T, Sasaki T, Kobayashi J (1992) Keramamide F, a new thiazole-containing peptide from the Okinawan marine sponge Theonella sp. J Org Chem 57: 5540-5542
    • (1992) J Org Chem , vol.57 , pp. 5540-5542
    • Itagaki, F.1    Shigemori, H.2    Ishibashi, M.3    Nakamura, T.4    Sasaki, T.5    Kobayashi, J.6
  • 300
    • 0028941534 scopus 로고
    • Keramamides E, G, H, and J, new cyclic peptides containing an oxazole or a thiazole ring from a Theonella sponge
    • Kobayashi J, Itagaki F, Shigemori H, Takao T, Shimonishi Y (1995) Keramamides E, G, H, and J, new cyclic peptides containing an oxazole or a thiazole ring from a Theonella sponge. Tetrahedron 51: 2525-2532
    • (1995) Tetrahedron , vol.51 , pp. 2525-2532
    • Kobayashi, J.1    Itagaki, F.2    Shigemori, H.3    Takao, T.4    Shimonishi, Y.5
  • 301
    • 0032507906 scopus 로고    scopus 로고
    • Keramamides K and L, new cyclic peptides containing unusual tryptophan residue from Theonella sponge
    • Uemoto H, Yahiro Y, Shigemori H, Tsuda M, Takao T, Shimonishi Y, Kobayashi J (1998) Keramamides K and L, new cyclic peptides containing unusual tryptophan residue from Theonella sponge. Tetrahedron 54: 6719-6724
    • (1998) Tetrahedron , vol.54 , pp. 6719-6724
    • Uemoto, H.1    Yahiro, Y.2    Shigemori, H.3    Tsuda, M.4    Takao, T.5    Shimonishi, Y.6    Kobayashi, J.7
  • 302
    • 0033595875 scopus 로고    scopus 로고
    • Keramamides M and N, two new cyclic peptides with a sulfate ester from Theonella sponge
    • Tsuda M, Ishiyama H, Masuko K, Takao T, Shimonishi Y, Kobayashi J (1999) Keramamides M and N, two new cyclic peptides with a sulfate ester from Theonella sponge. Tetrahedron 55: 12543-12548
    • (1999) Tetrahedron , vol.55 , pp. 12543-12548
    • Tsuda, M.1    Ishiyama, H.2    Masuko, K.3    Takao, T.4    Shimonishi, Y.5    Kobayashi, J.6
  • 305
    • 0037179166 scopus 로고    scopus 로고
    • Isolation of callipeltins A-C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins
    • Zampella A, Randazzo A, Borbone N, Luciani S, Trevisi L, Debitus C, D’Auria MV (2002) Isolation of callipeltins A-C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins. Tetrahedron Lett 43: 6163-6166
    • (2002) Tetrahedron Lett , vol.43 , pp. 6163-6166
    • Zampella, A.1    Randazzo, A.2    Borbone, N.3    Luciani, S.4    Trevisi, L.5    Debitus, C.6    D’Auria, M.V.7
  • 307
    • 37849188036 scopus 로고    scopus 로고
    • Isolation and structural elucidation of callipeltins J-M: Antifungal peptides from the marine sponge Latrunculia sp
    • D’Auria MV, Sepe V, D’Orsi R, Bellotta F, Debitus C, Zampella A (2007) Isolation and structural elucidation of callipeltins J-M: antifungal peptides from the marine sponge Latrunculia sp. Tetrahedron 63: 131-140
    • (2007) Tetrahedron , vol.63 , pp. 131-140
    • D’Auria, M.V.1    Sepe, V.2    D’Orsi, R.3    Bellotta, F.4    Debitus, C.5    Zampella, A.6
  • 310
    • 0035939149 scopus 로고    scopus 로고
    • Synthesis and analysis of the sterically constrained L-glutamine analogues (3 S,4R)-3,4-dimethyl-L-glutamine and (3 S,4R)-3,4-dimethyl-L-pyroglutamic acid
    • Acevedo CM, Kogut EF, Lipton MA (2001) Synthesis and analysis of the sterically constrained L-glutamine analogues (3 S,4R)-3,4-dimethyl-L-glutamine and (3 S,4R)-3,4-dimethyl-L-pyroglutamic acid. Tetrahedron 57: 6353-6359
    • (2001) Tetrahedron , vol.57 , pp. 6353-6359
    • Acevedo, C.M.1    Kogut, E.F.2    Lipton, M.A.3
  • 311
    • 0035855973 scopus 로고    scopus 로고
    • Chiron approach to callipeltin A: First synthesis of fully protected (2R,3R,4 S)-4,7-diamino-2,3-dihydroxyhepatonic acid
    • Chandrasekhar S, Ramachandar T, Venkateswara Rao B (2001) Chiron approach to callipeltin A: first synthesis of fully protected (2R,3R,4 S)-4,7-diamino-2,3-dihydroxyhepatonic acid. Tetrahedron: Assymetry 12: 2315-2321
    • (2001) Tetrahedron: Assymetry , vol.12 , pp. 2315-2321
    • Chandrasekhar, S.1    Ramachandar, T.2    Venkateswara Rao, B.3
  • 312
    • 0037007660 scopus 로고    scopus 로고
    • Progress towards the total synthesis of callipeltin A. Asymmetric synthesis of (2R,3R,4 S)-3-hydroxy-2,4,6-trimethylheptanoic acid
    • Guerlavais V, Carroll PJ, Joullié MM (2002) Progress towards the total synthesis of callipeltin A. Asymmetric synthesis of (2R,3R,4 S)-3-hydroxy-2,4,6-trimethylheptanoic acid. Tetrahedron: Assymetry 13: 675-680
    • (2002) Tetrahedron: Assymetry , vol.13 , pp. 675-680
    • Guerlavais, V.1    Carroll, P.J.2    Joullié, M.M.3
  • 313
    • 0037184887 scopus 로고    scopus 로고
    • Diastereoselective synthesis of all stereoisomers of b-methoxytyrosine, a component of papuamides
    • Okamoto N, Hara O, Makino K, Hamada Y (2002) Diastereoselective synthesis of all stereoisomers of b-methoxytyrosine, a component of papuamides. J Org Chem 67: 9210-9215
    • (2002) J Org Chem , vol.67 , pp. 9210-9215
    • Okamoto, N.1    Hara, O.2    Makino, K.3    Hamada, Y.4
  • 317
    • 0024996768 scopus 로고
    • Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A
    • Yoshida M, Kijima M, Akita M, Beppu T (1990) Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J Biol Chem 265: 17174-17179
    • (1990) J Biol Chem , vol.265 , pp. 17174-17179
    • Yoshida, M.1    Kijima, M.2    Akita, M.3    Beppu, T.4
  • 322
    • 0000181440 scopus 로고
    • The isoprene rule and the biogenesis of terpenic compounds
    • Ruzicka ZL (1953) The isoprene rule and the biogenesis of terpenic compounds. Experientia 9: 357-367
    • (1953) Experientia , vol.9 , pp. 357-367
    • Ruzicka, Z.L.1
  • 323
    • 84912291413 scopus 로고
    • The chemistry of marine animals. I. The sponge Microciona pralifera
    • Bergmann W, Johnson TB (1933) The chemistry of marine animals. I. The sponge Microciona pralifera. Z Physiol Chem 222: 220-226
    • (1933) Z Physiol Chem , vol.222 , pp. 220-226
    • Bergmann, W.1    Johnson, T.B.2
  • 324
    • 77649213543 scopus 로고    scopus 로고
    • Bioactive sesterterpenes and triterpenes from marine sponges: Occurrence and pharmacological significance
    • Ebada SS, Lin W, Proksch P (2010) Bioactive sesterterpenes and triterpenes from marine sponges: occurrence and pharmacological significance. Mar Drugs 8: 313-346
    • (2010) Mar Drugs , vol.8 , pp. 313-346
    • Ebada, S.S.1    Lin, W.2    Proksch, P.3
  • 325
    • 0018904327 scopus 로고
    • Manoalide, an antibiotic sesterterpenoid from the marine sponge Luffariella variabilis (Polejaeff)
    • De Silva ED, Scheuer PJ (1980) Manoalide, an antibiotic sesterterpenoid from the marine sponge Luffariella variabilis (Polejaeff). Tetrahedron Lett 21: 1611-1614
    • (1980) Tetrahedron Lett , vol.21 , pp. 1611-1614
    • De Silva, E.D.1    Scheuer, P.J.2
  • 326
    • 0019481753 scopus 로고
    • Three new sesterterpenoid antibiotics from the marine sponge Luffariella variabilis (Polejaeff)
    • De Silva ED, Scheuer PJ (1981) Three new sesterterpenoid antibiotics from the marine sponge Luffariella variabilis (Polejaeff). Tetrahedron Lett 22: 3147-3150
    • (1981) Tetrahedron Lett , vol.22 , pp. 3147-3150
    • De Silva, E.D.1    Scheuer, P.J.2
  • 327
    • 0023239402 scopus 로고
    • The luffariellins, novel anti-inflammatory sesterterpenes of chemotaxonomic importance from the marine sponge Luffariella variabilis
    • Kernan MR, Faulkner DJ, Jacobs RS (1987) The luffariellins, novel anti-inflammatory sesterterpenes of chemotaxonomic importance from the marine sponge Luffariella variabilis. J Org Chem 52: 3081-3083
    • (1987) J Org Chem , vol.52 , pp. 3081-3083
    • Kernan, M.R.1    Faulkner, D.J.2    Jacobs, R.S.3
  • 328
    • 0023223997 scopus 로고
    • Luffariellolide, an anti-inflammatory sesterterpene from the marine sponge Luffariella sp
    • Albizati KF, Holman T, Faulkner DJ, Glaser KB, Jacobs RS (1987) Luffariellolide, an anti-inflammatory sesterterpene from the marine sponge Luffariella sp. Experientia 43: 949-950
    • (1987) Experientia , vol.43 , pp. 949-950
    • Albizati, K.F.1    Holman, T.2    Faulkner, D.J.3    Glaser, K.B.4    Jacobs, R.S.5
  • 330
    • 0026565710 scopus 로고
    • Four new antibacterial sesterterpenes from a marine sponge of the genus Luffariella
    • Koenig GM, Wright AD, Sticher O (1992) Four new antibacterial sesterterpenes from a marine sponge of the genus Luffariella. J Nat Prod 55: 174-178
    • (1992) J Nat Prod , vol.55 , pp. 174-178
    • Koenig, G.M.1    Wright, A.D.2    Sticher, O.3
  • 331
    • 0026625768 scopus 로고
    • Luffalactone and (4E,6E)-dehydromanoalide from the sponge Luffariella variabilis
    • Potts BCM, Capon RJ, Faulkner DJ (1992) Luffalactone and (4E,6E)-dehydromanoalide from the sponge Luffariella variabilis. J Org Chem 57: 2965-2967
    • (1992) J Org Chem , vol.57 , pp. 2965-2967
    • Potts, B.C.M.1    Capon, R.J.2    Faulkner, D.J.3
  • 332
    • 84970614239 scopus 로고
    • The luffarins (A-Z), novel terpenes from an Australian marine sponge, Luffariella geometrica
    • Butler MS, Capon RJ (1992) The luffarins (A-Z), novel terpenes from an Australian marine sponge, Luffariella geometrica. Aust J Chem 45: 1705-1743
    • (1992) Aust J Chem , vol.45 , pp. 1705-1743
    • Butler, M.S.1    Capon, R.J.2
  • 333
    • 0026721551 scopus 로고
    • Luffariolides A-E, new cytotoxic sesterterpenes from the Okinawan marine sponge Luffariella sp
    • Tsuda M, Shigemori H, Ishibashi M, Sasaki T, Kobayashi J (1992) Luffariolides A-E, new cytotoxic sesterterpenes from the Okinawan marine sponge Luffariella sp. J Org Chem 57: 3503-3507
    • (1992) J Org Chem , vol.57 , pp. 3503-3507
    • Tsuda, M.1    Shigemori, H.2    Ishibashi, M.3    Sasaki, T.4    Kobayashi, J.5
  • 334
    • 0027468008 scopus 로고
    • Luffariolides F and G, new manoalide derivatives from the Okinawan marine sponge Luffariella sp
    • Kobayashi J, Zeng CM, Ishibashi M, Sasaki T (1993) Luffariolides F and G, new manoalide derivatives from the Okinawan marine sponge Luffariella sp. J Nat Prod 56: 436-439
    • (1993) J Nat Prod , vol.56 , pp. 436-439
    • Kobayashi, J.1    Zeng, C.M.2    Ishibashi, M.3    Sasaki, T.4
  • 335
    • 0002799327 scopus 로고    scopus 로고
    • Luffasterols A-C, 9,11-secosterols from the Palauan sponge Luffariella sp
    • Reddy MVR, Harper MK, Faulkner DJ (1997) Luffasterols A-C, 9,11-secosterols from the Palauan sponge Luffariella sp. J Nat Prod 60: 41-43
    • (1997) J Nat Prod , vol.60 , pp. 41-43
    • Reddy, M.V.R.1    Harper, M.K.2    Faulkner, D.J.3
  • 336
    • 0036773605 scopus 로고    scopus 로고
    • Luffariolides H and J, new sesterterpenes from a marine sponge Luffariella
    • Tsuda M, Endo T, Mikami Y, Fromont J, Kobayashi J (2002) Luffariolides H and J, new sesterterpenes from a marine sponge Luffariella. J Nat Prod 65: 1507-1508
    • (2002) J Nat Prod , vol.65 , pp. 1507-1508
    • Tsuda, M.1    Endo, T.2    Mikami, Y.3    Fromont, J.4    Kobayashi, J.5
  • 339
    • 58149263253 scopus 로고    scopus 로고
    • 24-O-Ethylmanoalide, a manoaliderelated sesterterpene from the marine sponge Luffariella cf. variabilis
    • Gauvin-Bialecki A, Aknin M, Smadja J (2008) 24-O-Ethylmanoalide, a manoaliderelated sesterterpene from the marine sponge Luffariella cf. variabilis. Molecules 13: 3184-3191
    • (2008) Molecules , vol.13 , pp. 3184-3191
    • Gauvin-Bialecki, A.1    Aknin, M.2    Smadja, J.3
  • 340
    • 0028216343 scopus 로고
    • Marine natural products. XXXII. Absolute configurations of C-4 of the manoalide family, biologically active sesterterpenes from the marine sponge Hyrtios erecta
    • Kobayashi M, Okamoto T, Hayashi K, Yokoyama N, Sasaki T, Kitagawa I (1994) Marine natural products. XXXII. Absolute configurations of C-4 of the manoalide family, biologically active sesterterpenes from the marine sponge Hyrtios erecta. Chem Pharm Bull 42: 265-270
    • (1994) Chem Pharm Bull , vol.42 , pp. 265-270
    • Kobayashi, M.1    Okamoto, T.2    Hayashi, K.3    Yokoyama, N.4    Sasaki, T.5    Kitagawa, I.6
  • 341
    • 2742564173 scopus 로고    scopus 로고
    • Biologically active sesterterpenes from a new Caledonian marine sponge Hyrtios sp
    • Bourguet-Kondracki ML, Debitus C, Guyot M (1996) Biologically active sesterterpenes from a new Caledonian marine sponge Hyrtios sp. J Chem Res 1996: 192-193
    • (1996) J Chem Res , vol.1996 , pp. 192-193
    • Bourguet-Kondracki, M.L.1    Debitus, C.2    Guyot, M.3
  • 342
    • 33845279760 scopus 로고
    • Chemistry of sponges, III. Manoalide monoacetate and thorectolide monoacetate, two new seterterpenoids from Thorectandra excavatus
    • Cambie RC, Craw PA, Bergquist PR, Karuso P (1988) Chemistry of sponges, III. Manoalide monoacetate and thorectolide monoacetate, two new seterterpenoids from Thorectandra excavatus. J Nat Prod 51: 331-334
    • (1988) J Nat Prod , vol.51 , pp. 331-334
    • Cambie, R.C.1    Craw, P.A.2    Bergquist, P.R.3    Karuso, P.4
  • 343
    • 0023751923 scopus 로고
    • Cacospongionolide: A new antitumoral sesterterpene, from the marine sponge Cacospongia mollior
    • De Rosa S, de Stefano S, Zavodnik N (1988) Cacospongionolide: a new antitumoral sesterterpene, from the marine sponge Cacospongia mollior. J Org Chem 53: 5020-5023
    • (1988) J Org Chem , vol.53 , pp. 5020-5023
    • De Rosa, S.1    de Stefano, S.2    Zavodnik, N.3
  • 345
    • 0028330125 scopus 로고
    • Fasciospongides A, B and C, new manoalide derivatives from the sponge Fasciospongia sp
    • Montagnac A, Païs M, Debitus C (1994) Fasciospongides A, B and C, new manoalide derivatives from the sponge Fasciospongia sp. J Nat Prod 57: 186-190
    • (1994) J Nat Prod , vol.57 , pp. 186-190
    • Montagnac, A.1    Païs, M.2    Debitus, C.3
  • 348
    • 32844459377 scopus 로고    scopus 로고
    • Two new luffarin derivatives from the Adriatic Sea sponge Fasciospongia cavernosa
    • De Rosa S, Carbonelli S (2006) Two new luffarin derivatives from the Adriatic Sea sponge Fasciospongia cavernosa. Tetrahedron 62: 2845-2849
    • (2006) Tetrahedron , vol.62 , pp. 2845-2849
    • De Rosa, S.1    Carbonelli, S.2
  • 350
    • 47549094913 scopus 로고    scopus 로고
    • Aplysinoplides A-C, cytotoxic sesterterpnes from the marine sponge Aplysinopsis digitata
    • Ueoka R, Nakao Y, Fujii S, van Soest RWM, Matsunaga S (2008) Aplysinoplides A-C, cytotoxic sesterterpnes from the marine sponge Aplysinopsis digitata. J Nat Prod 71: 1089-1091
    • (2008) J Nat Prod , vol.71 , pp. 1089-1091
    • Ueoka, R.1    Nakao, Y.2    Fujii, S.3    van Soest, R.W.M.4    Matsunaga, S.5
  • 351
    • 0021591782 scopus 로고
    • In vitro inactivation of the neurotoxic action of b-bungarotoxin by the marine natural product, manoalide
    • De Freitas JC, Blankemeier LA, Jacobs RS (1984) In vitro inactivation of the neurotoxic action of b-bungarotoxin by the marine natural product, manoalide. Experientia 40: 864-865
    • (1984) Experientia , vol.40 , pp. 864-865
    • De Freitas, J.C.1    Blankemeier, L.A.2    Jacobs, R.S.3
  • 352
    • 0022432248 scopus 로고
    • Cobra venom phospholipase A2 inhibition by manoalide. A novel type of phospholipase inhibitor
    • Lombardo D, Dennis EA (1985) Cobra venom phospholipase A2 inhibition by manoalide. A novel type of phospholipase inhibitor. J Biol Chem 260: 7234-7240
    • (1985) J Biol Chem , vol.260 , pp. 7234-7240
    • Lombardo, D.1    Dennis, E.A.2
  • 353
    • 0022596872 scopus 로고
    • Molecular pharmacology of manoalide. Inactivation of bee venom phospholipase A2
    • Glaser KB, Jacobs RS (1986) Molecular pharmacology of manoalide. Inactivation of bee venom phospholipase A2. Biochem Pharmacol 35: 449-453
    • (1986) Biochem Pharmacol , vol.35 , pp. 449-453
    • Glaser, K.B.1    Jacobs, R.S.2
  • 354
    • 0023237724 scopus 로고
    • Inactivation of bee venom phospholipase A2 by manoalide. A model based on the reactivity of manoalide with amino acids and peptide sequences
    • Glaser KB, Jacobs RS (1987) Inactivation of bee venom phospholipase A2 by manoalide. A model based on the reactivity of manoalide with amino acids and peptide sequences. Biochem Pharmacol 36: 2079-2086
    • (1987) Biochem Pharmacol , vol.36 , pp. 2079-2086
    • Glaser, K.B.1    Jacobs, R.S.2
  • 355
  • 356
    • 0024306483 scopus 로고
    • Manoalide:Structure-activity studies and definition of the pharmacophore for phospholipase A2 inactivation
    • Glaser KB, de Carvalho MS, Jacobs RS, Kernan MR, Faulkner DJ (1989) Manoalide:structure-activity studies and definition of the pharmacophore for phospholipase A2 inactivation. Mol Pharmacol 36: 782-788
    • (1989) Mol Pharmacol , vol.36 , pp. 782-788
    • Glaser, K.B.1    de Carvalho, M.S.2    Jacobs, R.S.3    Kernan, M.R.4    Faulkner, D.J.5
  • 357
    • 0025236785 scopus 로고
    • Inactivation of human synovial fluid phospholipase A2 by the marine natural product, manoalide
    • Jacobson PB, Marshall LA, Sung A, Jacobs RS (1990) Inactivation of human synovial fluid phospholipase A2 by the marine natural product, manoalide. Biochem Pharmacol 39: 1557-1564
    • (1990) Biochem Pharmacol , vol.39 , pp. 1557-1564
    • Jacobson, P.B.1    Marshall, L.A.2    Sung, A.3    Jacobs, R.S.4
  • 358
    • 0027181086 scopus 로고
    • Molecular model of the interaction of bee venom phospholipase A2 with manoalide
    • Ortiz AR, Pisabarro MT, Gago F (1993) Molecular model of the interaction of bee venom phospholipase A2 with manoalide. J Med Chem 36: 1866-1879
    • (1993) J Med Chem , vol.36 , pp. 1866-1879
    • Ortiz, A.R.1    Pisabarro, M.T.2    Gago, F.3
  • 361
    • 0027034136 scopus 로고
    • Phospholipase A2 inhibitors from marine organisms
    • Potts BCM, Faulkner DJ, Jacobs RS (1992) Phospholipase A2 inhibitors from marine organisms. J Nat Prod 55: 1701-1717
    • (1992) J Nat Prod , vol.55 , pp. 1701-1717
    • Potts, B.C.M.1    Faulkner, D.J.2    Jacobs, R.S.3
  • 362
    • 0025952114 scopus 로고
    • Inhibition of venom phospholipase A2 by manoalide and manoalogue
    • Reynolds LJ, Mihelich ED, Dennis EA (1991) Inhibition of venom phospholipase A2 by manoalide and manoalogue. J Biol Chem 266: 16512-16517
    • (1991) J Biol Chem , vol.266 , pp. 16512-16517
    • Reynolds, L.J.1    Mihelich, E.D.2    Dennis, E.A.3
  • 363
    • 0001225245 scopus 로고
    • Chemical mechanism of inactivation of bee venom phospholipase A2 by the marine natural products manoalide, luffariellolide, and scalaradial
    • Potts BCM, Faulkner DJ, de Carvalho MS, Jacobs RS (1992) Chemical mechanism of inactivation of bee venom phospholipase A2 by the marine natural products manoalide, luffariellolide, and scalaradial. J Am Chem Soc 114: 5093-5100
    • (1992) J Am Chem Soc , vol.114 , pp. 5093-5100
    • Potts, B.C.M.1    Faulkner, D.J.2    de Carvalho, M.S.3    Jacobs, R.S.4
  • 365
    • 0027118903 scopus 로고
    • Sponges to wipe away pain
    • Mann J (1992) Sponges to wipe away pain. Nature 358: 540
    • (1992) Nature , vol.358 , pp. 540
    • Mann, J.1
  • 366
    • 0033530145 scopus 로고    scopus 로고
    • Dysidiolide and related g-hydroxybutenolide compounds as inhibitors of the protein tyrosine phosphatase, CDC25
    • Blanchard JL, Epstein DM, Boisclair MD, Rudolph J, Pal K (1999) Dysidiolide and related g-hydroxybutenolide compounds as inhibitors of the protein tyrosine phosphatase, CDC25. Bioorg Med Chem Lett 9: 2537-2538
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 2537-2538
    • Blanchard, J.L.1    Epstein, D.M.2    Boisclair, M.D.3    Rudolph, J.4    Pal, K.5
  • 367
    • 0035015067 scopus 로고    scopus 로고
    • Thorectandrols A and B, new cytotoxic sesterterpenes from the marine sponge Thorectandra species
    • Charan RD, McKee TC, Boyd MR (2001) Thorectandrols A and B, new cytotoxic sesterterpenes from the marine sponge Thorectandra species. J Nat Prod 64: 661-663
    • (2001) J Nat Prod , vol.64 , pp. 661-663
    • Charan, R.D.1    McKee, T.C.2    Boyd, M.R.3
  • 368
    • 0036240214 scopus 로고    scopus 로고
    • Thorectandols C, D, and E, new sesterterpenes from the marine sponge Thorectandra sp
    • Charan RD, McKee TC, Boyd MR (2002) Thorectandols C, D, and E, new sesterterpenes from the marine sponge Thorectandra sp. J Nat Prod 65: 492-495
    • (2002) J Nat Prod , vol.65 , pp. 492-495
    • Charan, R.D.1    McKee, T.C.2    Boyd, M.R.3
  • 369
    • 0030720972 scopus 로고    scopus 로고
    • Further bioactive sesterterpenes from the Tyrrhenian sponge Fasciospongia cavernosa
    • De Rosa S, de Giulio A, Crispino A, Iodice C, Tommonaro G (1997) Further bioactive sesterterpenes from the Tyrrhenian sponge Fasciospongia cavernosa. Nat Prod Res 10: 267-274
    • (1997) Nat Prod Res , vol.10 , pp. 267-274
    • De Rosa, S.1    de Giulio, A.2    Crispino, A.3    Iodice, C.4    Tommonaro, G.5
  • 370
    • 0033805108 scopus 로고    scopus 로고
    • Synthetic applications of the thermal rearrangement of ozonides: First enantiospecific synthesis of marine metabolite Luffarin W
    • Barrero AF, Alvarez-Manzaneda EJ, Chahboun R, Cuerva JM, Segovia A (2000) Synthetic applications of the thermal rearrangement of ozonides: first enantiospecific synthesis of marine metabolite Luffarin W. Synlett 9: 1269-1272
    • (2000) Synlett , vol.9 , pp. 1269-1272
    • Barrero, A.F.1    Alvarez-Manzaneda, E.J.2    Chahboun, R.3    Cuerva, J.M.4    Segovia, A.5
  • 371
    • 33749324001 scopus 로고    scopus 로고
    • A unified strategy for the regiospecific assembly of homoallyl-substituted butenolides and g-hydroxybutenolides: First synthesis of luffariellolide
    • Boukouvalas J, Robichaud J, Maltais F (2006) A unified strategy for the regiospecific assembly of homoallyl-substituted butenolides and g-hydroxybutenolides: first synthesis of luffariellolide. Synlett 16: 2480-2482
    • (2006) Synlett , vol.16 , pp. 2480-2482
    • Boukouvalas, J.1    Robichaud, J.2    Maltais, F.3
  • 372
    • 33746337304 scopus 로고    scopus 로고
    • Terpenoids from marine organisms: Unique structures and their pharmacological potential
    • Gross H, Koenig GM (2006) Terpenoids from marine organisms: unique structures and their pharmacological potential. Phytochemistry Rev 5: 115-141
    • (2006) Phytochemistry Rev , vol.5 , pp. 115-141
    • Gross, H.1    Koenig, G.M.2
  • 373
    • 0344107519 scopus 로고
    • Variation of the metabolites of Chromodoris funerea: Comparison of specimen from a Palauan marine lake with those from adjacent waters
    • Kernan MR, Barrabee EB, Faulkner DJ (1988) Variation of the metabolites of Chromodoris funerea: comparison of specimen from a Palauan marine lake with those from adjacent waters. Comp Biochem Physiol 89B: 275-278
    • (1988) Comp Biochem Physiol , vol.89 B , pp. 275-278
    • Kernan, M.R.1    Barrabee, E.B.2    Faulkner, D.J.3
  • 374
    • 0020031344 scopus 로고
    • An antimicrobial sesterterpene from a Palauan sponge
    • Sullivan B, Faulkner DJ (1982) An antimicrobial sesterterpene from a Palauan sponge. Tetrahedron Lett 23: 907-910
    • (1982) Tetrahedron Lett , vol.23 , pp. 907-910
    • Sullivan, B.1    Faulkner, D.J.2
  • 375
    • 0029955176 scopus 로고    scopus 로고
    • Palauolol, a new anti-inflammatory sesterterpene from the sponge Fascaplysinopsis sp. from Palau
    • Schmidt EW, Faulkner DJ (1996) Palauolol, a new anti-inflammatory sesterterpene from the sponge Fascaplysinopsis sp. from Palau. Tetrahedron Lett 37: 3951-3954
    • (1996) Tetrahedron Lett , vol.37 , pp. 3951-3954
    • Schmidt, E.W.1    Faulkner, D.J.2
  • 376
    • 0029114237 scopus 로고
    • 25-Deoxycacospongionolide B and cacospongionolide C, two new terpenoids from the sponge Fasciospongia cavernosa
    • De Rosa S, Puliti R, Crispino A, de Giulio A, de Sena C, Iodice C, Mattia CA (1995) 25-Deoxycacospongionolide B and cacospongionolide C, two new terpenoids from the sponge Fasciospongia cavernosa. Tetrahedron 51: 10731-10736
    • (1995) Tetrahedron , vol.51 , pp. 10731-10736
    • De Rosa, S.1    Puliti, R.2    Crispino, A.3    de Giulio, A.4    de Sena, C.5    Iodice, C.6    Mattia, C.A.7
  • 377
    • 0028350817 scopus 로고
    • Sesterterpene lactones from a sponge species of the genus Dactylospongia
    • Lal AR, Cambie RC, Rickard CEF, Bergquist PR (1994) Sesterterpene lactones from a sponge species of the genus Dactylospongia. Tetrahedron Lett 35: 2603-2606
    • (1994) Tetrahedron Lett , vol.35 , pp. 2603-2606
    • Lal, A.R.1    Cambie, R.C.2    Rickard, C.E.F.3    Bergquist, P.R.4
  • 378
    • 0030107319 scopus 로고    scopus 로고
    • A sesterterpene lactone from Petrosaspongia nigra sp. nov
    • Cambie CR, Lal AR, Rickard CEF (1996) A sesterterpene lactone from Petrosaspongia nigra sp. nov. Acta Cryst C52: 709-711
    • (1996) Acta Cryst , vol.C52 , pp. 709-711
    • Cambie, C.R.1    Lal, A.R.2    Rickard, C.E.F.3
  • 379
    • 0030825329 scopus 로고    scopus 로고
    • New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist)
    • Gomez-Paloma L, Randazzo A, Minale L, Debitus C, Roussakis C (1997) New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist). Tetrahedron 53: 10451-10458
    • (1997) Tetrahedron , vol.53 , pp. 10451-10458
    • Gomez-Paloma, L.1    Randazzo, A.2    Minale, L.3    Debitus, C.4    Roussakis, C.5
  • 380
    • 0031777057 scopus 로고    scopus 로고
    • Petrosaspongiolodes M-R: New potent and selective phosphoplipase A2 inhibitors from the New Caledonian marine sponge Petrosaspongia nigra
    • Randazzo A, Debitus C, Minale L, Pastor PG, Alcaraz MJ, Payá M, Gomez-Paloma L (1998) Petrosaspongiolodes M-R: new potent and selective phosphoplipase A2 inhibitors from the New Caledonian marine sponge Petrosaspongia nigra. J Nat Prod 61: 571-575
    • (1998) J Nat Prod , vol.61 , pp. 571-575
    • Randazzo, A.1    Debitus, C.2    Minale, L.3    Pastor, P.G.4    Alcaraz, M.J.5    Payá, M.6    Gomez-Paloma, L.7
  • 381
    • 0034117962 scopus 로고    scopus 로고
    • New pyridinium alkaloids from a marine sponge of the genus Spongia with a human phospholipase A2 inhibitor profile
    • De Marino S, Iorizzi M, Zollo F, Debitus C, Menou JL, Ospina LF, Alcaraz MJ, Payá M (2000) New pyridinium alkaloids from a marine sponge of the genus Spongia with a human phospholipase A2 inhibitor profile. J Nat Prod 63: 322-326
    • (2000) J Nat Prod , vol.63 , pp. 322-326
    • De Marino, S.1    Iorizzi, M.2    Zollo, F.3    Debitus, C.4    Menou, J.L.5    Ospina, L.F.6    Alcaraz, M.J.7    Payá, M.8
  • 384
    • 1542301647 scopus 로고    scopus 로고
    • Further insights on the structural aspects of PLA2 inhibition by g-hydroxybutenolide-containing natural products:A comparative study of petrosaspongiolides M-R
    • Monti MC, Casapullo A, Riccio R, Gomez-Paloma L (2004) Further insights on the structural aspects of PLA2 inhibition by g-hydroxybutenolide-containing natural products:a comparative study of petrosaspongiolides M-R. Bioorg Med Chem 12: 1467-1474
    • (2004) Bioorg Med Chem , vol.12 , pp. 1467-1474
    • Monti, M.C.1    Casapullo, A.2    Riccio, R.3    Gomez-Paloma, L.4
  • 385
    • 10044279269 scopus 로고    scopus 로고
    • PLA2-mediated catalytic activation of its inhibitor 25-acetyl-petrosaspongiolide M: Serendipitous identification of a new PLA2 suicide inhibitor
    • Monti MC, Casapullo A, Riccio R, Gomez-Paloma L (2004) PLA2-mediated catalytic activation of its inhibitor 25-acetyl-petrosaspongiolide M: serendipitous identification of a new PLA2 suicide inhibitor. FEBS Lett 578: 269-274
    • (2004) FEBS Lett , vol.578 , pp. 269-274
    • Monti, M.C.1    Casapullo, A.2    Riccio, R.3    Gomez-Paloma, L.4
  • 386
    • 23844478640 scopus 로고    scopus 로고
    • Chemistry and biology of anti-inflammatory marine natural products. Phospholipase A2 inhibitors
    • Gomez-Paloma L, Monti MC, Terracciano S, Casapullo A, Riccio R (2005) Chemistry and biology of anti-inflammatory marine natural products. Phospholipase A2 inhibitors. Curr Org Chem 9: 1419-1427
    • (2005) Curr Org Chem , vol.9 , pp. 1419-1427
    • Gomez-Paloma, L.1    Monti, M.C.2    Terracciano, S.3    Casapullo, A.4    Riccio, R.5
  • 387
    • 58549101266 scopus 로고    scopus 로고
    • Effects of petrosaspongiolide R on the surface topology of bee venom PLA2: A limited proteolysis and mass spectrometry analysis
    • Monti MC, Riccio R, Casapullo A (2009) Effects of petrosaspongiolide R on the surface topology of bee venom PLA2: a limited proteolysis and mass spectrometry analysis. Bioorg Chem 37: 6-10
    • (2009) Bioorg Chem , vol.37 , pp. 6-10
    • Monti, M.C.1    Riccio, R.2    Casapullo, A.3
  • 388
    • 58449114054 scopus 로고    scopus 로고
    • The binding mode of petrosaspongiolide M to the human group IIA phospholipase A2: Exploring the role of covalent and noncovalent interactions in the inhibition process
    • Monti MC, Casapullo A, Cavasotto CN, Tosco A, Dal Piaz F, Ziemys A, Margarucci L, Riccio R (2009) The binding mode of petrosaspongiolide M to the human group IIA phospholipase A2: exploring the role of covalent and noncovalent interactions in the inhibition process. Chem Eur J 15: 1155-1163
    • (2009) Chem Eur J , vol.15 , pp. 1155-1163
    • Monti, M.C.1    Casapullo, A.2    Cavasotto, C.N.3    Tosco, A.4    Dal Piaz, F.5    Ziemys, A.6    Margarucci, L.7    Riccio, R.8
  • 389
    • 62249087105 scopus 로고    scopus 로고
    • Hemisynthesis of two marine cheilantane sesterterpenes from (-)-sclareol: First enantioselective synthesis of petrosaspongiolide R
    • Ferreiro-Mederos L, Lanners S, Henchiri H, Fekih A, Hanquet G (2009) Hemisynthesis of two marine cheilantane sesterterpenes from (-)-sclareol: first enantioselective synthesis of petrosaspongiolide R. Nat Prod Res 23: 256-263
    • (2009) Nat Prod Res , vol.23 , pp. 256-263
    • Ferreiro-Mederos, L.1    Lanners, S.2    Henchiri, H.3    Fekih, A.4    Hanquet, G.5
  • 390
    • 0002904994 scopus 로고
    • A new class of triterpenoids from Ailanthus malabarica DC. Derivatives of malabaricane
    • Chawla A, Dev S (1967) A new class of triterpenoids from Ailanthus malabarica DC. Derivatives of malabaricane. Tetrahedron Lett 8: 4837-4843
    • (1967) Tetrahedron Lett , vol.8 , pp. 4837-4843
    • Chawla, A.1    Dev, S.2
  • 391
    • 0742300313 scopus 로고
    • A direct correlation of (+)-malabaricol with (+)-ambreinolide
    • Sobti RR, Dev S (1968) A direct correlation of (+)-malabaricol with (+)-ambreinolide. Tetrahedron Lett 9: 2215-2217
    • (1968) Tetrahedron Lett , vol.9 , pp. 2215-2217
    • Sobti, R.R.1    Dev, S.2
  • 393
    • 0001720021 scopus 로고
    • Malabaricane triterpenes from a Fijian collection of the sponge Jaspis stellifera
    • Ravi BN, Wells RJ, Croft KD (1981) Malabaricane triterpenes from a Fijian collection of the sponge Jaspis stellifera. J Org Chem 46: 1998-2001
    • (1981) J Org Chem , vol.46 , pp. 1998-2001
    • Ravi, B.N.1    Wells, R.J.2    Croft, K.D.3
  • 394
    • 0000763074 scopus 로고
    • A triterpenoid pigment with the isomalabaricane skeleton from the marine sponge Stelletta sp
    • McCabe T, Clardy J, Minale L, Pizza C, Zollo F, Riccio R (1982) A triterpenoid pigment with the isomalabaricane skeleton from the marine sponge Stelletta sp. Tetrahedron Lett 23: 3307-3310
    • (1982) Tetrahedron Lett , vol.23 , pp. 3307-3310
    • McCabe, T.1    Clardy, J.2    Minale, L.3    Pizza, C.4    Zollo, F.5    Riccio, R.6
  • 395
    • 0030711053 scopus 로고    scopus 로고
    • Rhabdastrellic acid-A, a novel triterpenoid from the marine sponge Rhabdastrella globostellata
    • Rao Z, Deng S, Wu H, Jiang S (1997) Rhabdastrellic acid-A, a novel triterpenoid from the marine sponge Rhabdastrella globostellata. J Nat Prod 60: 1163-1164
    • (1997) J Nat Prod , vol.60 , pp. 1163-1164
    • Rao, Z.1    Deng, S.2    Wu, H.3    Jiang, S.4
  • 397
    • 0027974012 scopus 로고
    • Stellettin A, a new triterpenoid pigment from the marine sponge Stelletta tenuis
    • Su JY, Meng YH, Zeng LM, Fu X, Schmitz FJ (1994) Stellettin A, a new triterpenoid pigment from the marine sponge Stelletta tenuis. J Nat Prod 57: 1450-1451
    • (1994) J Nat Prod , vol.57 , pp. 1450-1451
    • Su, J.Y.1    Meng, Y.H.2    Zeng, L.M.3    Fu, X.4    Schmitz, F.J.5
  • 402
    • 33645996023 scopus 로고    scopus 로고
    • Bioactive isomalabaricane triterpenoids from Rhabdastrella globostellata that stabilize the binding of DNA polymerase b to DNA
    • Clement JA, Li M, Hecht SM, Kingston DGI (2006) Bioactive isomalabaricane triterpenoids from Rhabdastrella globostellata that stabilize the binding of DNA polymerase b to DNA. J Nat Prod 69: 373-376
    • (2006) J Nat Prod , vol.69 , pp. 373-376
    • Clement, J.A.1    Li, M.2    Hecht, S.M.3    Kingston, D.G.I.4
  • 403
    • 33746542436 scopus 로고    scopus 로고
    • Stellettin A induces oxidative stress and apoptosis in HL-60 human leukemia and LNCaP prostate cancer cell lines
    • Liu WK, Cheung FWK, Che CT (2006) Stellettin A induces oxidative stress and apoptosis in HL-60 human leukemia and LNCaP prostate cancer cell lines. J Nat Prod 69: 934-937
    • (2006) J Nat Prod , vol.69 , pp. 934-937
    • Liu, W.K.1    Cheung, F.W.K.2    Che, C.T.3
  • 404
    • 0034833558 scopus 로고    scopus 로고
    • Mitochrondrial transmembrane potential changes support the concept of mitochondrial heterogeneity during apoptosis
    • Krysko DV, Roels F, Leybaert L, D’Herde K (2001) Mitochrondrial transmembrane potential changes support the concept of mitochondrial heterogeneity during apoptosis. J Histochem Cytochem 49: 1277-1284
    • (2001) J Histochem Cytochem , vol.49 , pp. 1277-1284
    • Krysko, D.V.1    Roels, F.2    Leybaert, L.3    D’Herde, K.4
  • 405
    • 34548049515 scopus 로고    scopus 로고
    • Stellettins L and M, cytotoxic isomalabaricane-type triterpenes, and sterols from the marine sponge Stelletta tenuis
    • Lin HW, Wang ZL, Wu JH, Shi N, Zhang HJ, Chen WS, Morris-Natschke SL, Lin AS (2007) Stellettins L and M, cytotoxic isomalabaricane-type triterpenes, and sterols from the marine sponge Stelletta tenuis. J Nat Prod 70: 1114-1117
    • (2007) J Nat Prod , vol.70 , pp. 1114-1117
    • Lin, H.W.1    Wang, Z.L.2    Wu, J.H.3    Shi, N.4    Zhang, H.J.5    Chen, W.S.6    Morris-Natschke, S.L.7    Lin, A.S.8
  • 406
    • 56049091010 scopus 로고    scopus 로고
    • Rhabdastrellins A-F, isomalabaricane triterpenes from the marine sponge Rhabdastrella aff. distinca
    • Lv F, Xu M, Deng Z, de Voogd NJ, van Soest RWM, Proksch P, Lin WH (2008) Rhabdastrellins A-F, isomalabaricane triterpenes from the marine sponge Rhabdastrella aff. distinca. J Nat Prod 71: 1738-1741
    • (2008) J Nat Prod , vol.71 , pp. 1738-1741
    • Lv, F.1    Xu, M.2    Deng, Z.3    de Voogd, N.J.4    van Soest, R.W.M.5    Proksch, P.6    Lin, W.H.7
  • 407
    • 0026022356 scopus 로고
    • Stelliferins A-F, new antineoplastic isomalabaricane triterpenes from the Okinawan marine sponge Jaspis stellifera
    • Tsuda M, Ishibashi M, Agemi K, Sasaki T, Kobayashi J (1991) Stelliferins A-F, new antineoplastic isomalabaricane triterpenes from the Okinawan marine sponge Jaspis stellifera. Tetrahedron 47: 2181-2194
    • (1991) Tetrahedron , vol.47 , pp. 2181-2194
    • Tsuda, M.1    Ishibashi, M.2    Agemi, K.3    Sasaki, T.4    Kobayashi, J.5
  • 408
    • 0342614927 scopus 로고    scopus 로고
    • New isomalabaricane triterpenes from the marine sponge Stelletta globostellata that induce morphological changes in rat fibroblasts
    • Oku N, Matsunaga S, Wada SI, Watabe S, Fusetani N (2000) New isomalabaricane triterpenes from the marine sponge Stelletta globostellata that induce morphological changes in rat fibroblasts. J Nat Prod 63: 205-209
    • (2000) J Nat Prod , vol.63 , pp. 205-209
    • Oku, N.1    Matsunaga, S.2    Wada, S.I.3    Watabe, S.4    Fusetani, N.5
  • 409
    • 0035091235 scopus 로고    scopus 로고
    • New cytotoxic isomalabaricane triterpenes from the sponge Jaspis species
    • Meragelman KM, McKee TC, Boyd MR (2001) New cytotoxic isomalabaricane triterpenes from the sponge Jaspis species. J Nat Prod 64: 389-392
    • (2001) J Nat Prod , vol.64 , pp. 389-392
    • Meragelman, K.M.1    McKee, T.C.2    Boyd, M.R.3
  • 410
    • 0034973601 scopus 로고    scopus 로고
    • Stelliferin riboside, a triterpene monosaccharide isolated from the Fijian sponge Geodia globostellifera
    • Tabudravu JN, Jaspars M (2001) Stelliferin riboside, a triterpene monosaccharide isolated from the Fijian sponge Geodia globostellifera. J Nat Prod 64: 813-815
    • (2001) J Nat Prod , vol.64 , pp. 813-815
    • Tabudravu, J.N.1    Jaspars, M.2
  • 411
    • 0033609843 scopus 로고    scopus 로고
    • Synthesis of the trans-syn-trans perhydrobenz[e] indene moiety of the stellettins and the stelliferins
    • Raeppel F, Weibel JM, Heissler D (1999) Synthesis of the trans-syn-trans perhydrobenz[e] indene moiety of the stellettins and the stelliferins. Tetrahedron Lett 40: 6377-6381
    • (1999) Tetrahedron Lett , vol.40 , pp. 6377-6381
    • Raeppel, F.1    Weibel, J.M.2    Heissler, D.3
  • 412
    • 0029899219 scopus 로고    scopus 로고
    • Globostellatic acids A-D, new cytotoxic isomalabaricane triterpenes from the marine sponge Stelletta globostelleta
    • Ryu G, Matsunaga S, Fusetani N (1996) Globostellatic acids A-D, new cytotoxic isomalabaricane triterpenes from the marine sponge Stelletta globostelleta. J Nat Prod 59: 512-514
    • (1996) J Nat Prod , vol.59 , pp. 512-514
    • Ryu, G.1    Matsunaga, S.2    Fusetani, N.3
  • 413
  • 414
    • 34249676335 scopus 로고    scopus 로고
    • Novel isomalabaricane triterpenes, exhibiting selective anti-proliferative activity against vascular endothelial cells, from marine sponge Rhabdastrella globostellata
    • Aoki S, Sanagawa M, Watanabe Y, Setiawan A, Arai M, Kobayashi M (2007) Novel isomalabaricane triterpenes, exhibiting selective anti-proliferative activity against vascular endothelial cells, from marine sponge Rhabdastrella globostellata. Bioorg Med Chem 15: 4818-4828
    • (2007) Bioorg Med Chem , vol.15 , pp. 4818-4828
    • Aoki, S.1    Sanagawa, M.2    Watanabe, Y.3    Setiawan, A.4    Arai, M.5    Kobayashi, M.6
  • 415
    • 0035684349 scopus 로고    scopus 로고
    • Isomalabaricane-type nortriterpenoids and other constituents of the marine sponge Geodia japonica
    • Zhang WH, Che CT (2001) Isomalabaricane-type nortriterpenoids and other constituents of the marine sponge Geodia japonica. J Nat Prod 64: 1489-1492
    • (2001) J Nat Prod , vol.64 , pp. 1489-1492
    • Zhang, W.H.1    Che, C.T.2
  • 416
    • 11844263958 scopus 로고    scopus 로고
    • Isomalabaricane-type compounds from the marine sponge Rhabdastrella aff. distinca
    • Lv F, Deng Z, Li J, Fu H, van Soest RWM, Proksch P, Lin WH (2004) Isomalabaricane-type compounds from the marine sponge Rhabdastrella aff. distinca. J Nat Prod 67: 2033-2036
    • (2004) J Nat Prod , vol.67 , pp. 2033-2036
    • Lv, F.1    Deng, Z.2    Li, J.3    Fu, H.4    van Soest, R.W.M.5    Proksch, P.6    Lin, W.H.7
  • 417
    • 27144490732 scopus 로고    scopus 로고
    • Apoptotic activity of isomalabaricane triterpenes on human promyelocytic leukemia HL-60 cells
    • Liu WK, Ho JCK, Che CT (2005) Apoptotic activity of isomalabaricane triterpenes on human promyelocytic leukemia HL-60 cells. Cancer Lett 230: 102-110
    • (2005) Cancer Lett , vol.230 , pp. 102-110
    • Liu, W.K.1    Ho, J.C.K.2    Che, C.T.3
  • 418
    • 0030008240 scopus 로고    scopus 로고
    • Jaspiferals A-G, new cytotoxic isomalabaricane-type nortriterpenoids from Okinawan marine sponge Jaspis stellifera
    • Kobayashi J, Yuasa K, Kobayashi T, Sasaki T, Tsuda M (1996) Jaspiferals A-G, new cytotoxic isomalabaricane-type nortriterpenoids from Okinawan marine sponge Jaspis stellifera. Tetrahedron 52: 5745-5750
    • (1996) Tetrahedron , vol.52 , pp. 5745-5750
    • Kobayashi, J.1    Yuasa, K.2    Kobayashi, T.3    Sasaki, T.4    Tsuda, M.5
  • 419
    • 17544363911 scopus 로고    scopus 로고
    • New isomalabaricane derivatives from a new species of Jaspis sponge collected at the Vanuatu Islands
    • Zampella A, D’Auria MV, Debitus C, Menou JL (2000) New isomalabaricane derivatives from a new species of Jaspis sponge collected at the Vanuatu Islands. J Nat Prod 63: 943-946
    • (2000) J Nat Prod , vol.63 , pp. 943-946
    • Zampella, A.1    D’Auria, M.V.2    Debitus, C.3    Menou, J.L.4
  • 420
    • 0034701596 scopus 로고    scopus 로고
    • New cytotoxic isomalabaricane-type sesterterpenes from the new Caledonian marine sponge Rhabdastrella globostellata
    • Bourguet-Kondracki ML, Longeon A, Debitus C, Guyot M (2000) New cytotoxic isomalabaricane-type sesterterpenes from the new Caledonian marine sponge Rhabdastrella globostellata. Tetrahedron Lett 41: 3087-3090
    • (2000) Tetrahedron Lett , vol.41 , pp. 3087-3090
    • Bourguet-Kondracki, M.L.1    Longeon, A.2    Debitus, C.3    Guyot, M.4
  • 421
    • 29844453899 scopus 로고    scopus 로고
    • Jaspolides A-F, six new isomalabaricane-type terpenoids from the sponge Jaspis sp
    • Tang S, Pei Y, Fu H, Deng Z, Li J, Proksch P, Lin WH (2006) Jaspolides A-F, six new isomalabaricane-type terpenoids from the sponge Jaspis sp. Chem Pharm Bull 54: 4-8
    • (2006) Chem Pharm Bull , vol.54 , pp. 4-8
    • Tang, S.1    Pei, Y.2    Fu, H.3    Deng, Z.4    Li, J.5    Proksch, P.6    Lin, W.H.7
  • 422
    • 34347327048 scopus 로고    scopus 로고
    • Jaspolides G and H, unique bisisomalabaricanes from the Chinese marine sponge Jaspis sp
    • Tang S, Deng Z, Proksch P, Lin WH (2007) Jaspolides G and H, unique bisisomalabaricanes from the Chinese marine sponge Jaspis sp. Tetrahedron Lett 48: 5443-5447
    • (2007) Tetrahedron Lett , vol.48 , pp. 5443-5447
    • Tang, S.1    Deng, Z.2    Proksch, P.3    Lin, W.H.4
  • 423
    • 70349492061 scopus 로고    scopus 로고
    • Antileukemic activity of jaspolide B, an isomalabaricance-type triterpene from marine sponge Jaspis sp. on human promyeloleukemic HL-60 cells
    • Li M, Wei SY, Tang SA, Lin WH, Cui JR (2008) Antileukemic activity of jaspolide B, an isomalabaricance-type triterpene from marine sponge Jaspis sp. on human promyeloleukemic HL-60 cells. J Ch Pharm Sci 17: 11-15
    • (2008) J Ch Pharm Sci , vol.17 , pp. 11-15
    • Li, M.1    Wei, S.Y.2    Tang, S.A.3    Lin, W.H.4    Cui, J.R.5
  • 424
    • 65349173860 scopus 로고    scopus 로고
    • Induction of apoptosis accompanying with G1 phase arrest and microtubule disassembly in human hepatoma cells by jaspolide B, a new isomalabaricane-type triterpene
    • Wei SY, Li M, Tang SA, Sun W, Xu B, Cui JR, Lin WH (2008) Induction of apoptosis accompanying with G1 phase arrest and microtubule disassembly in human hepatoma cells by jaspolide B, a new isomalabaricane-type triterpene. Cancer Lett 262: 114-122
    • (2008) Cancer Lett , vol.262 , pp. 114-122
    • Wei, S.Y.1    Li, M.2    Tang, S.A.3    Sun, W.4    Xu, B.5    Cui, J.R.6    Lin, W.H.7
  • 426
    • 0026476576 scopus 로고
    • Potent inhibitors of histamine release, two novel triterpenoids from the Okinawan marine sponge Penares incrustans
    • Shoji N, Umeyama A, Motoki S, Arihara S, Ishida T, Nomoto K, Kobayashi J, Takei M (1992) Potent inhibitors of histamine release, two novel triterpenoids from the Okinawan marine sponge Penares incrustans. J Nat Prod 55: 1682-1685
    • (1992) J Nat Prod , vol.55 , pp. 1682-1685
    • Shoji, N.1    Umeyama, A.2    Motoki, S.3    Arihara, S.4    Ishida, T.5    Nomoto, K.6    Kobayashi, J.7    Takei, M.8
  • 427
    • 0026558374 scopus 로고
    • Structure characterization by two-dimensional NMR spectroscopy, of two marine triterpene oligosaccharides from a Pacific sponge of the genus Erylus
    • D’Auria MV, Paloma LG, Minale L, Riccio R, Debitus C (1992) Structure characterization by two-dimensional NMR spectroscopy, of two marine triterpene oligosaccharides from a Pacific sponge of the genus Erylus. Tetrahedron 48: 491-498
    • (1992) Tetrahedron , vol.48 , pp. 491-498
    • D’Auria, M.V.1    Paloma, L.G.2    Minale, L.3    Riccio, R.4    Debitus, C.5
  • 428
    • 0024563517 scopus 로고
    • The structure of eryloside A, a new antitumor and antifungal 4-methylated steroidal glycoside from the sponge Erylus lendenfeldi
    • Carmely S, Roll M, Loya Y, Kashman Y (1989) The structure of eryloside A, a new antitumor and antifungal 4-methylated steroidal glycoside from the sponge Erylus lendenfeldi. J Nat Prod 52: 167-170
    • (1989) J Nat Prod , vol.52 , pp. 167-170
    • Carmely, S.1    Roll, M.2    Loya, Y.3    Kashman, Y.4
  • 435
    • 0028019870 scopus 로고
    • A triterpene tetrasaccharide, formoside, from the Caribbean Choristida sponge Erylus formosus
    • Jaspars M, Crews P (1994) A triterpene tetrasaccharide, formoside, from the Caribbean Choristida sponge Erylus formosus. Tetrahedron Lett 35: 7501-7504
    • (1994) Tetrahedron Lett , vol.35 , pp. 7501-7504
    • Jaspars, M.1    Crews, P.2
  • 436
    • 0034703792 scopus 로고    scopus 로고
    • Triterpene glycosides defend the Caribbean reef sponge Erylus formosus from predatory fishes
    • Kubanek J, Pawlik JR, Eve TM, Fenical W (2000) Triterpene glycosides defend the Caribbean reef sponge Erylus formosus from predatory fishes. Mar Ecol Prog Ser 207: 69-77
    • (2000) Mar Ecol Prog Ser , vol.207 , pp. 69-77
    • Kubanek, J.1    Pawlik, J.R.2    Eve, T.M.3    Fenical, W.4
  • 437
    • 0036196283 scopus 로고    scopus 로고
    • Nobiloside, a new neuraminidase inhibitory triterpenoidal saponin from the marine sponge Erylus nobilis
    • Takada K, Nakao Y, Matsunaga S, van Soest RWM, Fusetani N (2002) Nobiloside, a new neuraminidase inhibitory triterpenoidal saponin from the marine sponge Erylus nobilis. J Nat Prod 65: 411-413
    • (2002) J Nat Prod , vol.65 , pp. 411-413
    • Takada, K.1    Nakao, Y.2    Matsunaga, S.3    van Soest, R.W.M.4    Fusetani, N.5
  • 438
    • 33745457515 scopus 로고    scopus 로고
    • Sokodosides, steroid glycosides with an isopropyl side chain, from the marine sponge Erylus placenta
    • Okada Y, Matsunaga S, van Soest RWM, Fusetani N (2006) Sokodosides, steroid glycosides with an isopropyl side chain, from the marine sponge Erylus placenta. J Org Chem 71: 4884-4888
    • (2006) J Org Chem , vol.71 , pp. 4884-4888
    • Okada, Y.1    Matsunaga, S.2    van Soest, R.W.M.3    Fusetani, N.4
  • 439
    • 35548933221 scopus 로고    scopus 로고
    • Oligosaccarides through reactivity tuning: Convergent synthesis of the trisaccharides of the steroid glycoside sokodoside B isolated from marine sponge Erylus placenta
    • Dasgupta S, Pramanik K, Mukhopadhyay B (2007) Oligosaccarides through reactivity tuning: convergent synthesis of the trisaccharides of the steroid glycoside sokodoside B isolated from marine sponge Erylus placenta. Tetrahedron 63: 12310-12316
    • (2007) Tetrahedron , vol.63 , pp. 12310-12316
    • Dasgupta, S.1    Pramanik, K.2    Mukhopadhyay, B.3
  • 440
    • 0023493214 scopus 로고
    • Structures of sarasinosides A1, B1, and C1; new norlanostane-triterpenoid oligosaccharides from the Palauan marine sponge Asteropus sarasinosum
    • Kitagawa I, Kobayashi M, Okamoto Y, Yoshikawa M, Hamamoto Y (1987) Structures of sarasinosides A1, B1, and C1; new norlanostane-triterpenoid oligosaccharides from the Palauan marine sponge Asteropus sarasinosum. Chem Pharm Bull 35: 5036-5039
    • (1987) Chem Pharm Bull , vol.35 , pp. 5036-5039
    • Kitagawa, I.1    Kobayashi, M.2    Okamoto, Y.3    Yoshikawa, M.4    Hamamoto, Y.5
  • 441
    • 0001029266 scopus 로고
    • Sarasinoside A1: A saponin containing amino sugars isolated from a sponge
    • Schmitz FJ, Ksebati MB, Gunasekera SP, Agarwal S (1988) Sarasinoside A1: a saponin containing amino sugars isolated from a sponge. J Org Chem 53: 5941-5947
    • (1988) J Org Chem , vol.53 , pp. 5941-5947
    • Schmitz, F.J.1    Ksebati, M.B.2    Gunasekera, S.P.3    Agarwal, S.4
  • 442
    • 0026319235 scopus 로고
    • Marine natural products. XXVIII. The structures of sarasinosides A1, A2, A3, B1, B2, B3, C1, C2, and C3, nine new norlanostanetriterpenoidal oligosaccharides from the Palauan marine sponge Asteropus sarasinosum
    • Kobayashi M, Okamoto Y, Kitagawa I (1991) Marine natural products. XXVIII. The structures of sarasinosides A1, A2, A3, B1, B2, B3, C1, C2, and C3, nine new norlanostanetriterpenoidal oligosaccharides from the Palauan marine sponge Asteropus sarasinosum. Chem Pharm Bull 39: 2867-2877
    • (1991) Chem Pharm Bull , vol.39 , pp. 2867-2877
    • Kobayashi, M.1    Okamoto, Y.2    Kitagawa, I.3
  • 443
    • 0026657986 scopus 로고
    • Sarasinosides D-G: Four new triterpenoid saponins from the sponge Asteropus sarasinosum
    • Espada A, Jiménez C, Rodríguez J, Crews P, Riguera R (1992) Sarasinosides D-G: four new triterpenoid saponins from the sponge Asteropus sarasinosum. Tetrahedron 48: 8685-8696
    • (1992) Tetrahedron , vol.48 , pp. 8685-8696
    • Espada, A.1    Jiménez, C.2    Rodríguez, J.3    Crews, P.4    Riguera, R.5
  • 445
    • 24744447004 scopus 로고    scopus 로고
    • Norlanostane triterpenoidal saponins from the marine sponge Melophlus sarassinorum
    • Dai HF, Edrada RA, Ebel R, Nimtz M, Wray V, Proksch P (2005) Norlanostane triterpenoidal saponins from the marine sponge Melophlus sarassinorum. J Nat Prod 68: 1231-1237
    • (2005) J Nat Prod , vol.68 , pp. 1231-1237
    • Dai, H.F.1    Edrada, R.A.2    Ebel, R.3    Nimtz, M.4    Wray, V.5    Proksch, P.6
  • 449
    • 0032801194 scopus 로고    scopus 로고
    • Ectyoplasides A-B-unique triterpene oligoglycosides from the Caribbean sponge Ectyoplasia ferox
    • Cafieri F, Fattorusso E, Taglialatela-Scafati O (1999) Ectyoplasides A-B-unique triterpene oligoglycosides from the Caribbean sponge Ectyoplasia ferox. Eur J Org Chem 1999: 231-238
    • (1999) Eur J Org Chem , vol.1999 , pp. 231-238
    • Cafieri, F.1    Fattorusso, E.2    Taglialatela-Scafati, O.3
  • 450
    • 0035971722 scopus 로고    scopus 로고
    • Feroxosides A-B, two norlanostane tetraglycosides from the Caribbean sponge Ectyoplasia ferox
    • Campagnuolo C, Fattorusso E, Taglialatela-Scafati O (2001) Feroxosides A-B, two norlanostane tetraglycosides from the Caribbean sponge Ectyoplasia ferox. Tetrahedron 57: 4049-4055
    • (2001) Tetrahedron , vol.57 , pp. 4049-4055
    • Campagnuolo, C.1    Fattorusso, E.2    Taglialatela-Scafati, O.3
  • 451
    • 0032575150 scopus 로고    scopus 로고
    • Ulososide B, a new unusual norlanostanetriterpene glycoside and its genuine aglycone from the Madagascar sponge Ulosa sp
    • Antonov AS, Kalinovsky AI, Stonik VA (1998) Ulososide B, a new unusual norlanostanetriterpene glycoside and its genuine aglycone from the Madagascar sponge Ulosa sp. Tetrahedron Lett 39: 3807-3808
    • (1998) Tetrahedron Lett , vol.39 , pp. 3807-3808
    • Antonov, A.S.1    Kalinovsky, A.I.2    Stonik, V.A.3
  • 453
    • 0033550207 scopus 로고    scopus 로고
    • Wondosterols A-C, three steroidal glycosides from a Korean marine two-sponge association
    • Ryu G, Choi BW, Lee BH, Hwang KH, Lee UC, Jeong DS, Lee NH (1999) Wondosterols A-C, three steroidal glycosides from a Korean marine two-sponge association. Tetrahedron 55: 13171-13178
    • (1999) Tetrahedron , vol.55 , pp. 13171-13178
    • Ryu, G.1    Choi, B.W.2    Lee, B.H.3    Hwang, K.H.4    Lee, U.C.5    Jeong, D.S.6    Lee, N.H.7
  • 454
    • 0025316261 scopus 로고
    • Structure of a novel steroidal saponin, pachastrelloside A, obtained from a marine sponge of the genus Pachastrella
    • Hirota H, Takayama S, Miyashiro S, Ozaki Y, Ikegami S (1990) Structure of a novel steroidal saponin, pachastrelloside A, obtained from a marine sponge of the genus Pachastrella. Tetrahedron Lett 31: 3321-3324
    • (1990) Tetrahedron Lett , vol.31 , pp. 3321-3324
    • Hirota, H.1    Takayama, S.2    Miyashiro, S.3    Ozaki, Y.4    Ikegami, S.5
  • 455
    • 0002224261 scopus 로고    scopus 로고
    • o-Conotoxin MVIIA: From marine snail venom to analgesic drug
    • Fusetani N (ed), Basel, Switzerland
    • Olivera BM (2000) o-Conotoxin MVIIA: from marine snail venom to analgesic drug. In:Fusetani N (ed) Drugs from the sea. Basel, Switzerland
    • (2000) Drugs from the sea
    • Olivera, B.M.1
  • 456
    • 0002829177 scopus 로고    scopus 로고
    • Aquacultural production of bryostatin 1 and ecteinascidin 743
    • Fusetani N (ed), Basel, Switzerland
    • Mendola D (2000) Aquacultural production of bryostatin 1 and ecteinascidin 743. In:Fusetani N (ed) Drugs from the Sea. Basel, Switzerland
    • (2000) Drugs from the Sea
    • Mendola, D.1
  • 457
    • 0344759904 scopus 로고
    • Chemical studies of marine bacteria: Developing a new resource
    • Fenical W (1993) Chemical studies of marine bacteria: developing a new resource. Chem Rev 93: 1673-1683
    • (1993) Chem Rev , vol.93 , pp. 1673-1683
    • Fenical, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.