메뉴 건너뛰기




Volumn , Issue , 2010, Pages 613-643

Marine natural products and their synthetic derivatives for cancer therapy

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84885748506     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-1-4419-0020-3_24     Document Type: Chapter
Times cited : (2)

References (143)
  • 1
    • 33947104489 scopus 로고    scopus 로고
    • Bioactive natural products from marine cyanobacteria for drug discovery
    • DOI 10.1016/j.phytochem.2007.01.012, PII S0031942207000519
    • Tan LT. Bioactive natural products from marine cyanobacteria for drug discovery. Phytochemistry (Elsevier). 2007;68(7):954-79. (Pubitemid 46413338)
    • (2007) Phytochemistry , vol.68 , Issue.7 , pp. 954-979
    • Tan, L.T.1
  • 3
    • 14744287300 scopus 로고    scopus 로고
    • Novel antitumor agents: Marine sponge alkaloids, their synthetic analogs and derivatives
    • Dembitsky VM, Gloriozova TA, Vladimir VP Novel antitumor agents: marine sponge alkaloids, their synthetic analogues and derivatives. Mini Rev Med Chem. 2005;5:319-36. (Pubitemid 40331048)
    • (2005) Mini-Reviews in Medicinal Chemistry , vol.5 , Issue.3 , pp. 319-336
    • Dembitsky, V.M.1    Gloriozova, T.A.2    Poroikov, V.V.3
  • 4
    • 9644278102 scopus 로고    scopus 로고
    • Marine pharmacology in 2001-2: Antitumour and cytotoxic compounds
    • DOI 10.1016/j.ejca.2004.09.005, PII S0959804904007464
    • Mayer AMS, Gustafson KR Marine pharmacology in 2001-2: antitumour and cytotoxic compounds. Eur J Cancer 2004;40:2676-704. (Pubitemid 39574721)
    • (2004) European Journal of Cancer , vol.40 , Issue.18 , pp. 2676-2704
    • Mayer, A.M.S.1    Gustafson, K.R.2
  • 5
    • 33748125863 scopus 로고    scopus 로고
    • Marine pharmacology in 2003-2004: Anti-tumour and cytotoxic compounds
    • DOI 10.1016/j.ejca.2006.05.019, PII S0959804906005193
    • Mayer AMS, Gustafson KR Marine pharmacology in 2003-2004: anti-tumour and cytotoxic compounds. Eur J Cancer 2006;42:2241-70. (Pubitemid 44307627)
    • (2006) European Journal of Cancer , vol.42 , Issue.14 , pp. 2241-2270
    • Mayer, A.M.S.1    Gustafson, K.R.2
  • 7
    • 0023409608 scopus 로고
    • Grossularine-1 and grossularine-2, carbolines from dendrodoa grossularia as possible interca-lative agents
    • Helbecque N, Moquin C, Bernier J.L., Morel E., et al Grossularine-1 and grossularine-2, carbolines from Dendrodoa grossularia as possible interca-lative agents. Cancer Biochem Biophys. 1987;9(3):271-9.
    • (1987) Cancer Biochem Biophys. , vol.9 , Issue.3 , pp. 271-279
    • Helbecque, N.1    Moquin, C.2    Bernier, J.L.3    Morel, E.4
  • 8
    • 0024394766 scopus 로고
    • Cytotoxic α-carbolines from the tunicate: Dendrodoa grossularia
    • Moquin-Pattey C., Guyot M. Cytotoxic α-carbolines from the tunicate: Dendrodoa grossularia. Tetrahedron 1989; 45 (11):3445-50.
    • (1989) Tetrahedron , vol.45 , Issue.11 , pp. 3445-3450
    • Moquin-Pattey, C.1    Guyot, M.2
  • 9
    • 27844463013 scopus 로고    scopus 로고
    • Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases
    • DOI 10.1016/j.lfs.2005.09.007, PII S0024320505008854
    • Gul W, Hamann MT Indole alkaloid marine natural products: an established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases. Life Sci. 2005;78:442-53. (Pubitemid 41653494)
    • (2005) Life Sciences , vol.78 , Issue.5 , pp. 442-453
    • Gul, W.1    Hamann, M.T.2
  • 11
    • 0029670813 scopus 로고    scopus 로고
    • Effects of beta-and gamma-carboline derivatives of DNA topoisomerase activities
    • Funayama Y, Nishio K, Wakabayashi K., Nagao M, et al Effects of beta-and gamma-carboline derivatives of DNA topoisomerase activities. Mutat Res. 1996;349:183-91.
    • (1996) Mutat Res. , vol.349 , pp. 183-191
    • Funayama, Y.1    Nishio, K.2    Wakabayashi, K.3    Nagao, M.4
  • 15
    • 0020043031 scopus 로고
    • Selective inhibition of in vitro synthesis of cancer DNA by alkaloids of β-carboline class
    • Beljanski M, Beljanski MS Selective inhibition of in vitro synthesis of cancer DNA by alkaloids of beta-carboline class. Exp Cell Biol. 1982;50:79-87. (Pubitemid 12185281)
    • (1982) Experimental Cell Biology , vol.50 , Issue.2 , pp. 79-87
    • Beljanski, M.1    Beljanski, M.S.2
  • 16
    • 0035952254 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of DNA targeting flexible side-chain substituted β-carboline derivatives
    • DOI 10.1016/S0960-894X(00)00679-X, PII S0960894X0000679X
    • Xiao S, Lin W, Wang C., Yang M. Synthesis and biological evaluation of DNA targeting flexible side-chain substituted β-carboline derivatives. Bioorg Med Chem Lett. 2001;11:437-41. (Pubitemid 32165203)
    • (2001) Bioorganic and Medicinal Chemistry Letters , vol.11 , Issue.4 , pp. 437-441
    • Xiao, S.1    Lin, W.2    Wang, C.3    Yang, M.4
  • 17
    • 0000853969 scopus 로고
    • Ascidians: Producers of amino acid-derived metabolites
    • Davidson BS. Ascidians: producers of amino acid-derived metabolites. Chem Rev. 1993;93:1771-91.
    • (1993) Chem Rev. , vol.93 , pp. 1771-1791
    • Davidson, B.S.1
  • 18
    • 33845282524 scopus 로고
    • Eudistomins A-Q, β-carbolines from the antiviral caribbean tunicate eudistoma oliva-ceum
    • Rinehart KL J.r., Kobayashi J, Harbour G.C., Gilmore J., et al Eudistomins A-Q, β-carbolines from the antiviral Caribbean tunicate Eudistoma oliva-ceum. J Am Chem Soc. 1987;109:3378-87.
    • (1987) J Am Chem Soc. , vol.109 , pp. 3378-3387
    • Rinehart Jr., K.L.1    Kobayashi, J.2    Harbour, G.C.3    Gilmore, J.4
  • 19
    • 0000602866 scopus 로고    scopus 로고
    • Structures and biogenesis of manzamines and related alkaloids
    • Tsuda M, Kobayashi J. Structures and biogenesis of manzamines and related alkaloids. Heterocycles 1997;46:765-94. (Pubitemid 127740650)
    • (1997) Heterocycles , vol.46 , Issue.1 , pp. 765-794
    • Tsuda, M.1    Kobayashi, J.2
  • 20
    • 0025744352 scopus 로고
    • Novel sponge-derived amino acids 12: Tryptophan-derived pigments and accompanying sesterterpenes from fascaplysinopsis reticulata
    • (a) Jimenez C, Quinoa E, Adamczeski M, Hunter LM, et al. Novel sponge-derived amino acids 12: tryptophan-derived pigments and accompanying sesterterpenes from Fascaplysinopsis reticulata. J Org Chem. 1991;56:3403-10.
    • (1991) J Org Chem. , vol.56 , pp. 3403-3410
    • Jimenez, C.1    Quinoa, E.2    Adamczeski, M.3    Hunter, L.M.4
  • 21
    • 0029885174 scopus 로고    scopus 로고
    • A new β-carboline alkaloid isolated from the marine sponge Hyrtios erecta
    • DOI 10.1016/0040-4039(96)00573-4
    • (b) Bourguet-Kondracki ML, Martin MT, Guyot M. A new-carboline alkaloid isolated from the marine sponge Hyrtios erecta. Tetrahedron Lett. 1996;37:3457-60. (Pubitemid 26164725)
    • (1996) Tetrahedron Letters , vol.37 , Issue.20 , pp. 3457-3460
    • Bourguet-Kondracki, M.L.1    Martin, M.T.2    Guyot, M.3
  • 22
    • 0036741295 scopus 로고    scopus 로고
    • Cytotoxic β-carboline and cyclic peroxides from the Palauan sponge plakortis nigra
    • Sandler JS, Colin PL, Hooper JNA, Faulkner DJ Cytotoxic β-carboline and cyclic peroxides from the Palauan sponge Plakortis nigra. J Nat Prod. 2002;65:1258-61.
    • (2002) J Nat Prod. , vol.65 , pp. 1258-1261
    • Sandler, J.S.1    Colin, P.L.2    Hooper, J.N.A.3    Faulkner, D.J.4
  • 25
    • 0032891198 scopus 로고    scopus 로고
    • New lamellarin alkaloids from the Australian ascidian, Didemnum chartaceum
    • DOI 10.1021/np9803530
    • Davis RH, Carroll AR, Pierens G.K., Quinn RJ New lamellarin alkaloids from the Australian ascidian, Didemnum chartaceum. J Nat Prod. 1999;62:419-24. (Pubitemid 29165215)
    • (1999) Journal of Natural Products , vol.62 , Issue.3 , pp. 419-424
    • Davis, R.A.1    Carroll, A.R.2    Pierens, G.K.3    Quinn, R.J.4
  • 26
    • 3142764930 scopus 로고    scopus 로고
    • A family of anticancer marine pyrrole alkaloids
    • Bailly C. A family of anticancer marine pyrrole alkaloids. Curr Med Chem Anti-Cancer Agents 2004;4:363-87.
    • (2004) Curr Med Chem Anti-Cancer Agents , vol.4 , pp. 363-387
    • Bailly, C.1
  • 27
    • 0242526064 scopus 로고    scopus 로고
    • Lamellarin D: A novel inhibitor of topoisomerase I
    • Facompre M, Tardy C, Bal-Mahieu C, Colson P., et al Lamellarin D: a novel inhibitor of topoisomerase I. Cancer Res. 2003;63:7392-99.
    • (2003) Cancer Res. , vol.63 , pp. 7392-7399
    • Facompre, M.1    Tardy, C.2    Bal-Mahieu, C.3    Colson, P.4
  • 28
    • 16244384633 scopus 로고    scopus 로고
    • Lamellarin D: A novel pro-apoptotic agent from marine origin insensitive to P-glycoprotein-mediated drug efflux
    • DOI 10.1016/j.canlet.2004.09.022
    • Vanhuyse M, Kluza J, Tardy C., Otero G, et al Lamellarin D: a novel pro-apoptotic agent from marine origin insensitive to P-glycoprotein-mediated drug efflux. Cancer Lett. 2005;221:165-75. (Pubitemid 40460403)
    • (2005) Cancer Letters , vol.221 , Issue.2 , pp. 165-175
    • Vanhuyse, M.1    Kluza, J.2    Tardy, C.3    Otero, G.4    Cuevas, C.5    Bailly, C.6    Lansiaux, A.7
  • 29
    • 0029761248 scopus 로고    scopus 로고
    • Polyaromatic alkaloids from marine invertebrates as cytotoxic compounds and inhibitors of multidrug resistance caused by P-glycoprotein
    • Quesada AR, Garcia Gravalos MD, Fernandez Puentes JL. Polyaromatic alkaloids from marine invertebrates as cytotoxic compounds and inhibitors of multidrug resistance caused by P-glycoprotein. Br J Cancer 1996;74:677-82. (Pubitemid 26300756)
    • (1996) British Journal of Cancer , vol.74 , Issue.5 , pp. 677-682
    • Quesada, A.R.1    Garcia Gravalos, M.D.2    Fernandez Puentes, J.L.3
  • 30
    • 1542524871 scopus 로고    scopus 로고
    • Ningalins A-D: Novel aromatic alkaloids from a western Australian ascidian of the genus didemnum
    • Kang H, Fenical W. Ningalins A-D: novel aromatic alkaloids from a Western Australian ascidian of the genus Didemnum. J Org Chem. 1997;62:3254.
    • (1997) J Org Chem. , vol.62 , pp. 3254
    • Kang, H.1    Fenical, W.2
  • 31
    • 0000907439 scopus 로고
    • New alkaloids of the lamellarin class from the marine ascidian didemnum chartaceum (Sluiter, 1909)
    • (a) Lindquist N, Fenical W, Van Duyne GD, Clady J. New alkaloids of the lamellarin class from the marine ascidian Didemnum chartaceum (Sluiter, 1909). J Org Chem. 1988;53:4570.
    • (1988) J Org Chem. , vol.53 , pp. 4570
    • Lindquist, N.1    Fenical, W.2    Van Duyne, G.D.3    Clady, J.4
  • 32
    • 84970609784 scopus 로고
    • Studies of Australian ascidians I. Six new lamellarin-class alkaloids from a colonial ascidian, Didemnum sp
    • (b) Carrol AR, Bowden BF, Coll JC. Studies of Australian ascidians I. Six new lamellarin-class alkaloids from a colonial ascidian, Didemnum sp. Aust J Chem. 1993;46:489.
    • (1993) Aust J Chem. , vol.46 , pp. 489
    • Carrol, A.R.1    Bowden, B.F.2    Coll, J.C.3
  • 33
    • 0342307108 scopus 로고    scopus 로고
    • Lamellarin-S: A new aromatic metabolite from an Australian tunicate, didemnum sp
    • (c) Urban S, Hobbs L, Hooper JNA, Capon RJ. Lamellarin-S: a new aromatic metabolite from an Australian tunicate, Didemnum sp. Aust J Chem. 1996;49:711.
    • (1996) Aust J Chem. , vol.49 , pp. 711
    • Urban, S.1    Hobbs, L.2    Hooper, J.N.A.3    Capon, R.J.4
  • 34
    • 0342742143 scopus 로고
    • Lamellarins Q and R: New aromatic metabolites from an Australian marine sponge, dendrilla cactos
    • (d) Urban S, Capon RJ. Lamellarins Q and R: new aromatic metabolites from an Australian marine sponge, Dendrilla cactos. Aust J Chem. 1995;48:1491.
    • (1995) Aust J Chem. , vol.48 , pp. 1491
    • Urban, S.1    Capon, R.J.2
  • 35
    • 0034697265 scopus 로고    scopus 로고
    • Total synthesis of Ningalin B utilizing a heterocyclic azadiene Diels-Alder reaction and discovery of a new class of potent multidrug resistant (MDR) reversal agents
    • DOI 10.1021/jo9916535
    • Boger DL, Soenen DR, Boyce C.W., Hedrick MP, et al Total synthesis of ningalin B utilizing a heterocyclic azadiene Diels-Alder reaction and discovery of a new class of potent multidrug resistant (MDR) reversal agents. J Org Chem. 2000;65:2479-83. (Pubitemid 30235817)
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.8 , pp. 2479-2483
    • Boger, D.L.1    Soenen, D.R.2    Boyce, C.W.3    Hedrick, M.P.4    Jin, Q.5
  • 36
    • 8844241601 scopus 로고    scopus 로고
    • Multidrug resistance reversal activity of permethyl ningalin B amide derivatives
    • DOI 10.1016/j.bmcl.2004.10.002, PII S0960894X04012259
    • Tao HC, Hwang I, Boger DL Multidrug resistance reversal activity of permethyl ningalin B amide derivatives. Bioorg Med Chem Lett. 2004;14:5979-81. (Pubitemid 39531255)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.24 , pp. 5979-5981
    • Tao, H.1    Hwang, I.2    Boger, D.L.3
  • 37
    • 0033550480 scopus 로고    scopus 로고
    • Total syntheses of ningalin A, lamellarin O, lukianol A, and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions
    • DOI 10.1021/ja982078+
    • Boger DL, Boyce CW, Labroli M.A., Sehon CA, et al Total syntheses of ningalin A, lamellarin O, lukianol A, and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions. J Am Chem Soc. 1999;121:54-62. (Pubitemid 29047122)
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.1 , pp. 54-62
    • Boger, D.L.1    Boyce, C.W.2    Labroli, M.A.3    Sehon, C.A.4    Jin, Q.5
  • 38
    • 0343058970 scopus 로고    scopus 로고
    • Storniamides A-D: Alkaloids from a patagonian sponge cliona sp
    • Palermo JA, Brasco MFR, Seldes AM Storniamides A-D: alkaloids from a Patagonian sponge Cliona sp. Tetrahedron 1996;52:2727.
    • (1996) Tetrahedron , vol.52 , pp. 2727
    • Palermo, J.A.1    Brasco, M.F.R.2    Seldes, A.M.3
  • 39
    • 0141432025 scopus 로고    scopus 로고
    • Efficient synthesis of enantiomerically pure 2-acylaziridines: Facile syntheses of N-Boc-safingol, N-Boc-D-erythro-sphinganine, and N-Boc-spisulosine from a common intermediate
    • DOI 10.1021/jo034755a
    • Yun JM, Sim TB, Hahm H.S., Lee WK, et al Efficient synthesis of enantio-merically pure 2-acylaziridines: facile syntheses of N-Boc-safingol, N-Boc-D-erythrosphinganine, and N-Boc-spisulosine from a common intermediate. J Org Chem. 2003;68:7675-80. (Pubitemid 37186117)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.20 , pp. 7675-7680
    • Yun, J.M.1    Sim, T.B.2    Hahm, H.S.3    Lee, W.K.4    Ha, H.-J.5
  • 40
    • 0034725101 scopus 로고    scopus 로고
    • The marine compound spisulosine, an inhibitor of cell proliferation, promotes the disassembly of actin stress fibers
    • DOI 10.1016/S0304-3835(99)00428-0, PII S0304383599004280
    • Cuadros R, Montejo de Garcini E, Wandosel F, Faircloth G, et al. The marine compound spisulosine, an inhibitor of cell proliferation, promotes the disassembly of actin stress fibers. Cancer Lett. 2000;152:23-9. (Pubitemid 30169014)
    • (2000) Cancer Letters , vol.152 , Issue.1 , pp. 23-29
    • Cuadros, R.1    Montejo De Garcini, E.2    Wandosell, F.3    Faircloth, G.4    Fernandez-Sousa, J.M.5    Avila, J.6
  • 41
    • 4344650390 scopus 로고    scopus 로고
    • Marine natural products and related compounds in clinical and advanced preclinical trials
    • DOI 10.1021/np040031y
    • Newman DJ, Cragg GM Marine natural products and related compounds in clinical and advanced preclinical trial. J Nat Prod. 2004;67:1216-38. (Pubitemid 39145623)
    • (2004) Journal of Natural Products , vol.67 , Issue.8 , pp. 1216-1238
    • Newman, D.J.1    Cragg, G.M.2
  • 45
    • 0141953928 scopus 로고    scopus 로고
    • The discovery of NVP-LAQ824: From concept to clinic
    • DOI 10.2174/0929867033456675
    • Remiszewski SW. The discovery of NVP-LAQ824: from concept to clinic. Curt Med Chem. 2003;10:2393-402. (Pubitemid 37236395)
    • (2003) Current Medicinal Chemistry , vol.10 , Issue.22 , pp. 2393-2402
    • Remiszewski, S.W.1
  • 46
    • 11144316651 scopus 로고    scopus 로고
    • The novel histone deacetylase inhibitor NVP-LAQ824: An addition to the therapeutic armamentarium in leukemia?
    • DOI 10.1038/sj.leu.2403522
    • Grant S. The novel histone deacetylase inhibitor NVP-LAQ824: an addition to the therapeutic armamentarium in leukemia. Leukemia 2004;18(12):1931-3. (Pubitemid 40028417)
    • (2004) Leukemia , vol.18 , Issue.12 , pp. 1931-1933
    • Grant, S.1
  • 49
    • 0036270039 scopus 로고    scopus 로고
    • ET-743: More than an innovative mechanism of action
    • Seotto KW. ET-743: more than an innovative mechanism of action. Anticancer Drugs 2002;13:S3-S6.
    • (2002) Anticancer Drugs , vol.13
    • Seotto, K.W.1
  • 50
    • 0034786774 scopus 로고    scopus 로고
    • Sequence-dependent enhancement of cytotoxicity produced by ecteinascidin 743 (ET-743) with doxorubicin or paclitaxel in soft tissue sarcoma cells
    • Takahashi N, Li WW, Banerjee D, et al Sequence-dependent enhancement of cytotoxicity produced by ecteinascidin 743 (ET-743) with doxorubicin or paclitaxel in soft tissue sarcoma cells. Clin Cancer Res. 2001;7:3251-7. (Pubitemid 32963850)
    • (2001) Clinical Cancer Research , vol.7 , Issue.10 , pp. 3251-3257
    • Takahashi, N.1    Li, W.W.2    Banerjee, D.3    Scotto, K.W.4    Bertino, J.R.5
  • 51
    • 0036277072 scopus 로고    scopus 로고
    • Safety and efficacy of ET-743: The french experience
    • Brain EG. Safety and efficacy of ET-743: the French experience. Anticancer Drugs 2002;13:Sll-S14.
    • (2002) Anticancer Drugs , vol.13
    • Brain, E.G.1
  • 53
    • 0036314931 scopus 로고    scopus 로고
    • Drugs from the seas: Current status and microbiological implications
    • Proksch P, Edrada RA, Ebel R. Drugs from the seas: current status and microbiological implications. Appl Microb Biotech. 2002;59(2):l25-34.
    • (2002) Appl Microb Biotech. , vol.59 , Issue.2
    • Proksch, P.1    Edrada, R.A.2    Ebel, R.3
  • 55
    • 0028356202 scopus 로고
    • The synthesis of branched steroidal prodrugs of nitrogen mustard for antitumor targeting via reconstituted LDL
    • DOI 10.1016/S0040-4039(00)60717-7
    • Dubowchik GM, Firesone RA The synthesis of branched steroidal pro-drugs of nitrogen mustard for antitumor targeting via reconstituted LDL. Tetrahedron Lett. 1994;35:4523-6. (Pubitemid 24203115)
    • (1994) Tetrahedron Letters , vol.35 , Issue.26 , pp. 4523-4526
    • Dubowchik, G.M.1    Firestone, R.A.2
  • 56
    • 0021884581 scopus 로고
    • Ellipticine derivatives with an affinity to the estrogen receptor, an approach to develop intercalating drugs with a specific effect on the hormone-dependent breast cancer
    • DOI 10.1021/jm00383a011
    • Delbarre A, Oberlin R, Roques B. Ellipticine derivatives with an affinity to the estrogen receptor, an approach to develop intercalating drugs with a specific effect on the hormone-dependent breast cancer. J Med Chem. 1985;28:752-61. (Pubitemid 15026116)
    • (1985) Journal of Medicinal Chemistry , vol.28 , Issue.6 , pp. 752-761
    • Delbarre, A.1    Oberlin, R.2    Roques, B.P.3
  • 57
    • 0033644299 scopus 로고    scopus 로고
    • Outer-ring stereochemical modulation of cytotoxicity in cephalostatin
    • Thmas GL, Guo C, Boyd M.R., Fuchs PL Outer-ring stereochemical modulation of cytotoxicity in cephalostatin. Org Lett. 2000;2(1):33-6.
    • (2000) Org Lett. , vol.2 , Issue.1 , pp. 33-36
    • Thmas, G.L.1    Guo, C.2    Boyd, M.R.3    Fuchs, P.L.4
  • 58
    • 0035137292 scopus 로고    scopus 로고
    • Marine natural products
    • DOI 10.1039/b006897g
    • Faulkner DJ. Marine natural products. Nat Prod Rep. 2001;18:1-49. (Pubitemid 32160982)
    • (2001) Natural Product Reports , vol.18 , Issue.1 , pp. 1-49
    • Faulkner, D.J.1
  • 59
    • 0001229636 scopus 로고
    • Polyoxygenated steroids of marine origin
    • D'Auria M.V., Minale L, Riccio R. Polyoxygenated steroids of marine origin. Chem Rev. 1993;93:1839-95.
    • (1993) Chem Rev. , vol.93 , pp. 1839-1895
    • D'Auria, M.V.1    Minale, L.2    Riccio, R.3
  • 62
    • 0035907721 scopus 로고    scopus 로고
    • Total synthesis of agosterol A: An MDR-modulator from a marine sponge
    • Nobutoshi M, Masanori S, Mari M., Motomasa K. Total synthesis of agosterol A: an MDR-modulator from a marine sponge. Chemistry-A Eur J. 2001; 7 (12):2663-70.
    • (2001) Chemistry-A Eur J. , vol.7 , Issue.12 , pp. 2663-2670
    • Nobutoshi, M.1    Masanori, S.2    Mari, M.3    Motomasa, K.4
  • 64
    • 0033520950 scopus 로고    scopus 로고
    • Reversal of multidrug resistance in human carcinoma cell line by agosterols, marine spongean sterols
    • Aoki S, Setiawan A, Yoshioka Y., Higuchi K, et al Reversal of multidrug resistance in human carcinoma cell line by agosterols, marine spongean sterols. Tetrahedron 1999;55:13965-72.
    • (1999) Tetrahedron , vol.55 , pp. 13965-13972
    • Aoki, S.1    Setiawan, A.2    Yoshioka, Y.3    Higuchi, K.4
  • 69
    • 33745418150 scopus 로고    scopus 로고
    • Expression of basic fibroblast growth factor correlates with resistance to paclitaxel in human patient tumors
    • DOI 10.1007/s11095-006-0136-6
    • Gan Y, Wientjes MG, Au JL-S. Expression of basic fibroblast growth factor correlates with resistance to paclitaxel in human patient tumors. Pharm Res. 2006;23(6):1324-31. (Pubitemid 43946154)
    • (2006) Pharmaceutical Research , vol.23 , Issue.6 , pp. 1324-1331
    • Gan, Y.1    Wientjes, M.G.2    Au, J.L.-S.3
  • 70
    • 22644439708 scopus 로고    scopus 로고
    • Chemistry and biology of bile acids
    • Mukhopadhyay S, Maitra U. Chemistry and biology of bile acids. Curr Sci. 2004;87(12):1666-83. (Pubitemid 41024553)
    • (2004) Current Science , vol.87 , Issue.12 , pp. 1666-1683
    • Mukhopadhyay, S.1    Maitra, U.2
  • 71
    • 0029999237 scopus 로고    scopus 로고
    • Structural studies by exciton coupled circular dichroism over a large distance: Porphyrin derivatives of steroids, dimeric steroids, and brevetoxin B
    • DOI 10.1021/ja960126p
    • Matile J, Beroua N, Nakanishi K., Wood R. Structural studies by exciton coupled circular dichroism over a large distance: porphyrin derivatives of steroids, dimeric steroids, and brevetoxin B. J Am Chem Soc. 1996;118:5198-206. (Pubitemid 26201540)
    • (1996) Journal of the American Chemical Society , vol.118 , Issue.22 , pp. 5198-5206
    • Matile, S.1    Berova, N.2    Nakanishi, K.3    Fleischhauer, J.4    Woody, R.W.5
  • 72
    • 0000591172 scopus 로고
    • A water soluble dimeric steroid with catalytic properties, rate enhancements from hydrophobic binding
    • Guthre JP, Cossa J, Darson BA A water soluble dimeric steroid with catalytic properties, rate enhancements from hydrophobic binding. Can J Chem. 1986;64:2456-69.
    • (1986) Can J Chem. , vol.64 , pp. 2456-2469
    • Guthre, J.P.1    Cossa, J.2    Darson, B.A.3
  • 73
    • 0026735902 scopus 로고
    • Simple procedure for reductive coupling of steroids with a cross-conjugated dienone system
    • Schmidt A, Beckert A, Weiss RD Simple procedure for reductive coupling of steroids with a cross-conjugated dienone system. Tetrahedron Lett. 1992;33:4299-300.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4299-4300
    • Schmidt, A.1    Beckert, A.2    Weiss, R.D.3
  • 75
    • 0029085998 scopus 로고
    • Isolation and structure of the exceptional pterobranchia human cancer inhibitors cephalostatins 16 and 1
    • Pettit JM, Xu JP, Schmidt JM Isolation and structure of the exceptional Pterobranchia human cancer inhibitors cephalostatins 16 and 1. Bioorg Med Chem Lett. 1995;5:2027-30.
    • (1995) Bioorg Med Chem Lett. , vol.5 , pp. 2027-2030
    • Pettit, J.M.1    Xu, J.P.2    Schmidt, J.M.3
  • 76
    • 0037129408 scopus 로고    scopus 로고
    • A convenient synthesis of C-22 and sterioisomers of cephalostatin north 1 side chain from spirostan sapogenin
    • Camen B, Raimunda F, Perez-Martin I, Tierry P., et al A convenient synthesis of C-22 and sterioisomers of cephalostatin north 1 side chain from spirostan sapogenin. Org Lett. 2002;4(8):1295-8.
    • (2002) Org Lett. , vol.4 , Issue.8 , pp. 1295-1298
    • Camen, B.1    Raimunda, F.2    Perez-Martin, I.3    Tierry, P.4
  • 77
    • 0000097162 scopus 로고    scopus 로고
    • Dimeric and oligomeric steroids
    • Yuexian L, Dias JR Dimeric and oligomeric steroids. Chem Rev. 1997;97:283-304. (Pubitemid 127662447)
    • (1997) Chemical Reviews , vol.97 , Issue.1 , pp. 283-304
    • Li, Y.1    Dias, J.R.2
  • 78
    • 41549141298 scopus 로고    scopus 로고
    • Synthesis of bis-diosgenin pyrazine dimers: New cephalostatin analogs
    • Shawakfeh KQ, Al-Said NH, Al-Zoubi RM. Synthesis of bis-diosgenin pyrazine dimers: new cephalostatin analogs. Steroids 2008;73(6):579-84.
    • (2008) Steroids , vol.73 , Issue.6 , pp. 579-584
    • Shawakfeh, K.Q.1    Al-Said, N.H.2    Al-Zoubi, R.M.3
  • 79
    • 0000137196 scopus 로고
    • Marine biotechnology. Antitumor and cytotoxic compounds from marine organisms
    • Schmitz FJ, Bowden FJ, Toth SI Marine biotechnology. Antitumor and cytotoxic compounds from marine organisms. Mar Biotechnol. 1993;1:197-308.
    • (1993) Mar Biotechnol. , vol.1 , pp. 197-308
    • Schmitz, F.J.1    Bowden, F.J.2    Toth, S.I.3
  • 80
    • 0019470678 scopus 로고
    • Structures of the didemnins, antiviral and cytotoxic depsipeptides from a Caribbean tunicate
    • DOI 10.1021/ja00397a055
    • Rinehart KL, Gloer JB, Cook J.C., Mizsak SA, et al Structures of the didemnins, antiviral and cytotoxic depsipeptides from a Caribbean tunicate. J Am Chem Soc. 1981;103:1857-9. (Pubitemid 11075621)
    • (1981) Journal of the American Chemical Society , vol.103 , Issue.7 , pp. 1857-1859
    • Rinehart Jr., K.L.1    Gloer, J.B.2    Cook Jr., J.C.3
  • 83
    • 0028139458 scopus 로고
    • Ritterazine A, a highly cytotoxic dimeric steroidal alkaloid, from the tunicate Ritterella tokioka
    • DOI 10.1021/jo00100a014
    • Fukuzawa S, Matsunaga S, Fusetani N. A highly cytotoxic dimeric steroi-dal alkaloid, from the tunicate Ritterella tokioka. J Org Chem. 1994; 59 (21):6164-6. (Pubitemid 24351134)
    • (1994) Journal of Organic Chemistry , vol.59 , Issue.21 , pp. 6164-6166
    • Fukuzawa, S.1    Matsunaga, S.2    Fusetani, N.3
  • 84
    • 33748242750 scopus 로고    scopus 로고
    • The dimeric steroid-pyrazine marine alkaloids: Challenges for isolation, synthesis, and biological studies
    • Ganesan A. The dimeric steroid-pyrazine marine alkaloids: challenges for isolation, synthesis, and biological studies. Angew Chem Int Ed Engl. 1996;35(6):611-15. (Pubitemid 126665365)
    • (1996) Angewandte Chemie (International Edition in English) , vol.35 , Issue.6 , pp. 611-615
    • Ganesan, A.1
  • 89
    • 0036383653 scopus 로고    scopus 로고
    • The cyanobacterial origin of potent anticancer agents originally isolated from sea hares
    • Luesch H, Harrigan GG, Goetz G, Horgen FD. The cyanobacterial origin of potent anticancer agents originally isolated from sea hares. Curr Med Chem. 2002;9:1791-806.
    • (2002) Curr Med Chem. , vol.9 , pp. 1791-1806
    • Luesch, H.1    Harrigan, G.G.2    Goetz, G.3    Horgen, F.D.4
  • 90
    • 0041692511 scopus 로고    scopus 로고
    • Natural products from marine invertebrates: The Harbor Branch Oceanographic Institution experience
    • (c) Sennett SH, McCarthy PJ, Wright AE, Pomponi SA. Natural products from marine invertebrates: the harbor branch oceanographic institution experience. Pharm News 2002;9:483-8. (Pubitemid 37107980)
    • (2002) Pharmaceutical News , vol.9 , Issue.6 , pp. 483-488
    • Sennett, S.H.1    McCarthy, P.J.2    Wright, A.E.3    Pomponi, S.A.4
  • 91
    • 0042193219 scopus 로고    scopus 로고
    • Current marine pharmacology contributions to new drug development in the biopharmaceutical industry
    • (d) Mayer AMS. Current marine pharmacology contributions to new drug development in the biopharmaceutical industry. Pharm News 2002;9:479-82.
    • (2002) Pharm News , vol.9 , pp. 479-482
    • Mayer, A.M.S.1
  • 92
    • 0038219974 scopus 로고    scopus 로고
    • Marine pharmacology in 2000: Antitumor and cytotoxic compounds
    • DOI 10.1002/ijc.11080
    • (e) Mayer AMS, Gustafson KR. Marine pharmacology in 2000: antitumor and cytotoxic compounds. Int J Cancer 2003;105:291-9. (Pubitemid 36570039)
    • (2003) International Journal of Cancer , vol.105 , Issue.3 , pp. 291-299
    • Mayer, A.M.S.1    Gustafson, K.R.2
  • 94
    • 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 D.L., Cerny RL, et al Antineoplastic agents 277, isolation and structure of phakellistatin 3 and isophakellistatin 3 from a Republic of Comoros marine sponge. J Org Chem. 1994;59:1593.
    • (1994) J Org Chem. , vol.59 , pp. 1593
    • Pettit, G.R.1    Tan, R.2    Herald, D.L.3    Cerny, R.L.4
  • 95
    • 0001240801 scopus 로고
    • Antineoplastic agents 303, isolation and structure of the human cell growth inhibitory phakellistatin 4 from the western pacific sponge phakellia costata
    • Pettit GR, Xu JP, Cichacz Z, Schmidt J.M., et al Antineoplastic agents 303, isolation and structure of the human cell growth inhibitory phakellistatin 4 from the western Pacific sponge Phakellia costata. Heterocycles 1994;40:501.
    • (1994) Heterocycles , vol.40 , pp. 501
    • Pettit, G.R.1    Xu, J.P.2    Cichacz, Z.3    Schmidt, J.M.4
  • 96
    • 0019470678 scopus 로고
    • Structures of the didemnins, antiviral and cytotoxic depsipeptides from a Caribbean tunicate
    • DOI 10.1021/ja00397a055
    • Rinehart KL, Gloer JB, Cook J.C., Mizsak SA, et al Structures of the didemnins, antiviral and cytotoxic depsipeptides from a Caribbean tunicate. J Am Chem Soc. 1981;103:1857-9. (Pubitemid 11075621)
    • (1981) Journal of the American Chemical Society , vol.103 , Issue.7 , pp. 1857-1859
    • Rinehart Jr., K.L.1    Gloer, J.B.2    Cook Jr., J.C.3
  • 97
    • 0019469697 scopus 로고
    • Didemnins: Antiviral and antitumor depsipeptides from a Caribbean tunicate
    • Rinehart KL, Gloer JB, Hughes R.G., Renis HE, et al Didemnins: antiviral and antitumor depsipeptides from a Caribbean tunicate. Science 1981;212:933-5. (Pubitemid 11120478)
    • (1981) Science , vol.212 , Issue.4497 , pp. 933-935
    • Rinehart Jr., K.L.1    Gloer, J.B.2    Hughes Jr., R.G.3
  • 98
    • 0033981511 scopus 로고    scopus 로고
    • Antitumor compounds from tunicates
    • DOI 10.1002/(SICI)1098-1128(200001)20:1<1::AID-MED1>3.0.CO;2-A
    • Rinehart KL. Antitumor compounds from tunicates. Med Res Rev. 2000;20:1-27. (Pubitemid 30027559)
    • (2000) Medicinal Research Reviews , vol.20 , Issue.1 , pp. 1-27
    • Rinehart, K.L.1
  • 99
    • 0036178591 scopus 로고    scopus 로고
    • Natural products as probes of cell biology: 20 Years of didemnin research
    • DOI 10.1002/med.10003
    • Vera MD, Joullie MM Natural products as probes of cell biology: 20 years of didemnin research. Med Res Rev. 2002;22:102-45. (Pubitemid 34160582)
    • (2002) Medicinal Research Reviews , vol.22 , Issue.2 , pp. 102-145
    • Vera, M.D.1    Joullie, M.M.2
  • 101
    • 84885786699 scopus 로고    scopus 로고
    • Rinehart KL, Lithgow-Bertelloni AM, Dehydrodidemnin B. WO 9104985; 1991
    • Rinehart KL, Lithgow-Bertelloni AM, Dehydrodidemnin B. WO 9104985; 1991.
  • 102
    • 2542500409 scopus 로고    scopus 로고
    • Phase I trials with aplidine, a new marine derived anticancer compound
    • Raymond E, Paz-Ares L, Izquierdo M., Belanger K, et al Phase I trials with aplidine, a new marine derived anticancer compound. Eur J Can. 2001;37 Suppl 6:S32.
    • (2001) Eur J Can. , vol.37 , Issue.SUPPL. 6
    • Raymond, E.1    Paz-Ares, L.2    Izquierdo, M.3    Belanger, K.4
  • 103
    • 0040573218 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of aplidine, a marine derived compound, given as a 24 h infusion every 2 weeks in patients (pts) with advanced solid tumors and non-hodgkin lymphoma (NHL)
    • Raymond E, Ady-Vago N, Ribrag V., Faivre S, et al Phase I and pharmacokinetic study of aplidine, a marine derived compound, given as a 24 h infusion every 2 weeks in patients (pts) with advanced solid tumors and non-Hodgkin lymphoma (NHL). Ann Oncol. 2000;11 Suppl 4:134.
    • (2000) Ann Oncol. , vol.11 , Issue.SUPPL. 4 , pp. 134
    • Raymond, E.1    Ady-Vago, N.2    Ribrag, V.3    Faivre, S.4
  • 104
    • 0039980349 scopus 로고    scopus 로고
    • A phase I study of aplidine (APL), a marine derived compound, given as an infusion weekly x 3 in advanced solid tumors and non-hodgkin lymphoma patients (pts)
    • Izquierdo MA, Bowman A, Martínez M, Cicchella B., et al A phase I study of aplidine (APL), a marine derived compound, given as an infusion weekly x 3 in advanced solid tumors and non-Hodgkin lymphoma patients (pts). Ann Oncol. 2000;11 Suppl 4:134.
    • (2000) Ann Oncol. , vol.11 , Issue.SUPPL. 4 , pp. 134
    • Izquierdo, M.A.1    Bowman, A.2    Martínez, M.3    Cicchella, B.4
  • 105
    • 0142234465 scopus 로고    scopus 로고
    • Phase I study of aplidine (APL) in a 1 hour daily infusion x 5 q 3 weeks in patients (pts) with solid tumors and low intermediate grade non hodgkins lymphomas: A national cancer institute of Canada-clinical trials group (NCIC-CTG) study
    • Maroun J, Belanger K, Seymour L., Soulieres D, et al Phase I study of aplidine (APL) in a 1 hour daily infusion x 5 q 3 weeks in patients (pts) with solid tumors and low intermediate grade non Hodgkins lymphomas: a National Cancer Institute of Canada-Clinical Trials Group (NCIC-CTG) study. Ann Oncol. 2000;11 Suppl 4:134.
    • (2000) Ann Oncol. , vol.11 , Issue.SUPPL. 4 , pp. 134
    • Maroun, J.1    Belanger, K.2    Seymour, L.3    Soulieres, D.4
  • 106
    • 0037513401 scopus 로고    scopus 로고
    • Tasipeptins A and B: New cytotoxic depsipeptides from the marine cyanobacterium Symploca sp
    • DOI 10.1021/np020582t
    • Williams PG, Yoshida WY, Moore R.E., Paul VJ Tasipeptins A and B: new cytotoxic depsipeptides from the marine cyanobacterium Symploca sp. J Nat Prod. 2003;66:620-4. (Pubitemid 36617883)
    • (2003) Journal of Natural Products , vol.66 , Issue.5 , pp. 620-624
    • Williams, P.G.1    Yoshida, W.Y.2    Moore, R.E.3    Paul, V.J.4
  • 107
    • 0035225541 scopus 로고    scopus 로고
    • Nitrogen-containing metabolites from marine cyanobacteria
    • PII S0099959801570030
    • Gerwick WH, Tan LT, Sitachitta N, Cordell GA Nitrogen-containing metabolites from marine cyanobacteria. In: Cordell GA, editor. The Alkaloids. San Diego: Academic Press; 2001. Vol. 57, pp. 75-184. (Pubitemid 33805341)
    • (2001) Alkaloids: Chemistry and Biology , vol.57 , pp. 75-184
    • Gerwick, W.H.1    Tong Tan, L.2    Sitachitta, N.3
  • 108
    • 1642546939 scopus 로고    scopus 로고
    • Scleritodermin A, a cytotoxic cyclic peptide from the lithistid sponge scleritoderma nodosum
    • Schmidt EW, Raventos SC, Bifano M, Menendez A.T., et al Scleritodermin A, a cytotoxic cyclic peptide from the lithistid sponge Scleritoderma nodosum. J Nat Prod. 2004;67:475.
    • (2004) J Nat Prod. , vol.67 , pp. 475
    • Schmidt, E.W.1    Raventos, S.C.2    Bifano, M.3    Menendez, A.T.4
  • 109
    • 0028826185 scopus 로고
    • Macro-cyclic peptide inhibitors of serine proteases, convergent total synthesis of cyclotheonamides A and B via a late-stage primary amine intermediate. Study of thrombin inhibition under diverse conditions
    • Maryanoff BE, Greco MN, Zhang H.C., Andrade-Gordon P, et al Macro-cyclic peptide inhibitors of serine proteases, convergent total synthesis of cyclotheonamides A and B via a late-stage primary amine intermediate. Study of thrombin inhibition under diverse conditions. J Am Chem Soc. 1995;117:1225.
    • (1995) J Am Chem Soc. , vol.117 , pp. 1225
    • Maryanoff, B.E.1    Greco, M.N.2    Zhang, H.C.3    Andrade-Gordon, P.4
  • 110
    • 0027167091 scopus 로고
    • Inhibition of thrombin and other trypsin-like serine proteinases by cyclotheonamide A
    • Lewis SD, Ng AS, Baldwin J.J., Fusetani N., et al Inhibition of thrombin and other trypsin-like serine proteinases by cyclotheonamide A. Thromb Res. 1993;70:173.
    • (1993) Thromb Res. , vol.70 , pp. 173
    • Lewis, S.D.1    Ng, A.S.2    Baldwin, J.J.3    Fusetani, N.4
  • 111
    • 0026575932 scopus 로고
    • The mechanism of action of cyclosporin A and FK506
    • Schreiber SL, Crabtree GR The mechanism of action of cyclosporin A and FK506. Immunol Today 1992;13:136.
    • (1992) Immunol Today , vol.13 , pp. 136
    • Schreiber, S.L.1    Crabtree, G.R.2
  • 112
    • 0025997529 scopus 로고
    • Mechanisms ofresistance to etoposide and teniposide in acquired resistant human colon and lung carcinoma cell lines
    • Long BH, Wang L, Lorico A, Wang RR, et al. Mechanisms ofresistance to etoposide and teniposide in acquired resistant human colon and lung carcinoma cell lines. Cancer Res. 1991;51:5275-84.
    • (1991) Cancer Res. , vol.51 , pp. 5275-5284
    • Long, B.H.1    Wang, L.2    Lorico, A.3    Wang, R.R.4
  • 113
    • 0028305511 scopus 로고
    • Hemiasterlin and geodiamolide TA; two new cytotoxic peptides from the marine sponge hemiasterella minor (Kirkpatrick)
    • DOI 10.1016/S0040-4039(00)73382-X
    • Talpir R, Benayahu Y, Kashman Y., Pannell L, et al Hemiasterlin and geodiamolide TA; two new cytotoxic peptides from the marine sponge Hemiasterella minor (Kirkpatrick). Tetrahedron Lett. 1994;35:4453-6. (Pubitemid 24195061)
    • (1994) Tetrahedron Letters , vol.35 , Issue.25 , pp. 4453-4456
    • Talpir, R.1    Benayahu, Y.2    Kashman, Y.3    Pannell, L.4    Schleyer, M.5
  • 114
    • 0029090211 scopus 로고
    • Cytotoxic peptides from the marine sponge cymbastela sp
    • Coleman JE, de Silva ED, Kong FM, Andersen RJ, et al Cytotoxic peptides from the marine sponge Cymbastela sp. Tetrahedron 1995; 51 (39):10653-62.
    • (1995) Tetrahedron , vol.51 , Issue.39 , pp. 10653-10662
    • Coleman, J.E.1    De Silva, E.D.2    Kong, F.M.3    Andersen, R.J.4
  • 115
    • 0031060389 scopus 로고    scopus 로고
    • Cytotoxic peptides hemiasterlin, hemiasterlin A and hemiasterlin B induce mitotic arrest and abnormal spindle formation
    • DOI 10.1007/s002800050564
    • Anderson HJ, Coleman JE, Andersen R.J., Roberge M. Cytotoxic peptides hemiasterlin, hemiasterlin A, and hemiasterlin B include mitotic arrest and abnormal spindle formation. Cancer Chemother Pharmacol. 1997; 39 (3):223-6. (Pubitemid 26414259)
    • (1997) Cancer Chemotherapy and Pharmacology , vol.39 , Issue.3 , pp. 223-226
    • Anderson, H.J.1    Coleman, J.E.2    Andersen, R.J.3    Roberge, M.4
  • 118
    • 0346396114 scopus 로고    scopus 로고
    • The structure of Palau'amide, a potent cytotoxin from a species of the marine cyanobacter-ium lyngbya
    • Williams PG, Yoshida WY, Quon M.K., Moore RE, et al The structure of palau'amide, a potent cytotoxin from a species of the marine cyanobacter-ium Lyngbya. J Nat Prod. 2003;66:1545.
    • (2003) J Nat Prod. , vol.66 , pp. 1545
    • Williams, P.G.1    Yoshida, W.Y.2    Quon, M.K.3    Moore, R.E.4
  • 119
    • 12244287902 scopus 로고    scopus 로고
    • Isolation and structure of the cytotoxic cycloheptapeptide phakellistatin 13
    • Li WL, Yi YH, Wu H.M., Xu QZ, et al Isolation and structure of the cytotoxic cycloheptapeptide phakellistatin 13. J Nat Prod. 2003;66:146-8.
    • (2003) J Nat Prod. , vol.66 , pp. 146-148
    • Li, W.L.1    Yi, Y.H.2    Wu, H.M.3    Xu, Q.Z.4
  • 120
    • 12944265406 scopus 로고    scopus 로고
    • Isolation and structure of phakellistatin 14 from the western pacific marine sponge Phakellia sp
    • DOI 10.1021/np040092w
    • Pettit GR, Tan R. Isolation and structure of phakellistatin 14 from the western Pacific marine sponge Phakellia sp. J Nat Prod. 2005;68:60-3. (Pubitemid 40175930)
    • (2005) Journal of Natural Products , vol.68 , Issue.1 , pp. 60-63
    • Pettit, G.R.1    Tan, R.2
  • 121
    • 0029134951 scopus 로고
    • Isolation and structure of the human cancer cell growth inhibitory cyclic octapeptides phakellis-tatin 10 and 11 from phakellia sp
    • Pettit GR, Tan R, Ichihara Y., Williams MD, et al Isolation and structure of the human cancer cell growth inhibitory cyclic octapeptides phakellis-tatin 10 and 11 from Phakellia sp. J Nat Prod. 1995;58(6):961-5.
    • (1995) J Nat Prod. , vol.58 , Issue.6 , pp. 961-965
    • Pettit, G.R.1    Tan, R.2    Ichihara, Y.3    Williams, M.D.4
  • 124
    • 0026356420 scopus 로고
    • Antineoplastic agents. 219. Isolation and structure of the cell growth inhibitory constituents from the western pacific marine sponge axinella sp
    • Pettit GR, Herald CL, Boyd M.R., Leet JE, et al Antineoplastic agents. 219. Isolation and structure of the cell growth inhibitory constituents from the Western Pacific marine sponge Axinella sp. J Med Chem. 1991;34:3339-40.
    • (1991) J Med Chem. , vol.34 , pp. 3339-3340
    • Pettit, G.R.1    Herald, C.L.2    Boyd, M.R.3    Leet, J.E.4
  • 125
    • 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.I., Mikami Y., et al Hymenamides A and B, new proline-rich cyclic heptapeptides from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 1993;49:2391-402.
    • (1993) Tetrahedron , vol.49 , pp. 2391-2402
    • Kobayashi, J.1    Tsuda, M.2    Nakamura, T.I.3    Mikami, Y.4
  • 126
    • 0027182909 scopus 로고
    • New cyclic heptapeptides with two proline residues from the okinawan marine sponge hymeniacidon sp
    • Tsuda M, Shigemori H, Mikami Y., Kobayashi J. Hymenamides CE. New cyclic heptapeptides with two proline residues from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 1993;49:6785-96.
    • (1993) Tetrahedron , vol.49 , pp. 6785-6796
    • Tsuda, M.1    Shigemori, H.2    Mikami, Y.3    Kobayashi, J.4    Hymenamides, C.E.5
  • 127
    • 0028222655 scopus 로고
    • Hymenamides G, H, J, and K, four new cyclic octapeptides from the Okinawan marine sponge Hymeniacidon sp.
    • DOI 10.1016/S0040-4020(01)85006-7
    • Tsuda M, Sasaki T, Kobayashi J. Hymenamides G, H, J, and K, four new cyclic octapeptides from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron 1994;49:4667-80. (Pubitemid 24152189)
    • (1994) Tetrahedron , vol.50 , Issue.16 , pp. 4667-4680
    • Tsuda, M.1    Sasaki, T.2    Kobayashi, J.3
  • 128
    • 0029967644 scopus 로고    scopus 로고
    • Hymenamide F, new cyclic heptapeptide from marine sponge Hymeniacidon sp.
    • DOI 10.1016/0040-4020(96)00281-5
    • Kobayashi J, Nakamura T, Tsuda M. Hymenamide F, new cyclic hepta-peptide from marine sponge Hymeniacidon sp. Tetrahedron 1996;52:6355-60. (Pubitemid 26127806)
    • (1996) Tetrahedron , vol.52 , Issue.18 , pp. 6355-6360
    • Kobayashi, J.1    Nakamura, T.2    Tsuda, M.3
  • 129
    • 0028277872 scopus 로고
    • Pseudostellarin G, a new tyrosinase inhibitory cyclic octapeptide from Pseudostellaria heterophylla
    • DOI 10.1016/S0040-4039(00)73238-2
    • Morita H, Kobata H, Takeya K., Itokawa H. Cyclic peptides from higher plants. V. Pseudostellarin G, a new tyrosinase inhibitory cyclic octapeptide from Pseudostellaria heterophylla. Tetrahedron Lett. 1994;35:3563-4. (Pubitemid 24176483)
    • (1994) Tetrahedron Letters , vol.35 , Issue.21 , pp. 3563-3564
    • Morita, H.1    Kobata, H.2    Takeya, K.3    Itokawa, H.4
  • 130
    • 0027998785 scopus 로고
    • Pseudostellarins A-C, new tyrosinase inhibitory cyclic peptides from Pseudostellaria heterophylla
    • DOI 10.1016/S0040-4020(01)81333-8
    • Morita H, Kayashita T, Kobata H., Gonda A, et al Cyclic peptides from higher plants. VI. Pseudostellarins A-C, new tyrosinase inhibitory cyclic peptides from Pseudostellaria heterophylla. Tetrahedron 1994;50:6797-804. (Pubitemid 24293175)
    • (1994) Tetrahedron , vol.50 , Issue.23 , pp. 6797-6804
    • Morita, H.1    Kayashita, T.2    Kobata, H.3    Gonda, A.4    Takeya, K.5    Itokawa, H.6
  • 131
    • 0029874164 scopus 로고    scopus 로고
    • Cyclic peptides from higher plants. 29. Cycloleonuripeptides from leonurus heterophyllus
    • Morita H, Gonda A, Takeya K., Itokawa H. Cyclic peptides from higher plants. 29. Cycloleonuripeptides from Leonurus heterophyllus. Bioorg Med Chem Lett. 1996;6:767-70.
    • (1996) Bioorg Med Chem Lett. , vol.6 , pp. 767-770
    • Morita, H.1    Gonda, A.2    Takeya, K.3    Itokawa, H.4
  • 132
    • 0030054259 scopus 로고    scopus 로고
    • Cyclic peptides from higher plants. 26. Dichotomins A-E, new cyclic peptides from stellaria dichotoma L. Var. Lanceolata bge
    • Morita H, Kayashita T, Shishido A., Takeya K, et al Cyclic peptides from higher plants. 26. Dichotomins A-E, new cyclic peptides from Stellaria dichotoma L. var. lanceolata Bge. Tetrahedron 1996;52:1165-76.
    • (1996) Tetrahedron , vol.52 , pp. 1165-1176
    • Morita, H.1    Kayashita, T.2    Shishido, A.3    Takeya, K.4
  • 135
    • 0030842197 scopus 로고    scopus 로고
    • Three cyclopeptides from stellaria delavayi
    • DOI 10.1016/S0031-9422(96)00581-X, PII S003194229600581X
    • Zhao YR, Zhou J, Wang X.K., Wu HM, et al Three cyclopeptides from Stellaria delavayi. Phytochemistry 1997;46:709-14. (Pubitemid 27483833)
    • (1997) Phytochemistry , vol.46 , Issue.4 , pp. 709-714
    • Zhao, Y.-R.1    Zhou, J.2    Wang, X.-K.3    Wu, H.M.4    Huang, X.-L.5    Zou, C.6
  • 136
    • 20444477224 scopus 로고    scopus 로고
    • Synthesis, structure, and biological aspects of cyclopeptides related to marine phakellistatins 7-9
    • DOI 10.1016/j.tet.2005.04.067, PII S0040402005007623
    • Napolitano A, Bruno I, Riccio R., Gomez-Paloma L. Synthesis, structure, and biological aspects of cyclopeptides related to marine phakellistatins 7-9. Tetrahedron 2005;61:6808-15. (Pubitemid 40823019)
    • (2005) Tetrahedron , vol.61 , Issue.28 , pp. 6808-6815
    • Napolitano, A.1    Bruno, I.2    Riccio, R.3    Gomez-Paloma, L.4
  • 137
    • 0037351833 scopus 로고    scopus 로고
    • Trichodermamides A and B, cytotoxic modified dipeptides from the marine-derived fungus Trichoderma virens
    • DOI 10.1021/np0204390
    • Garo E, Starks CM, Jensen P.R., Fenical W., et al Trichodermamides A and B, cytotoxic modified dipeptides from the marine-derived fungus Tricho-derma virens. J Nat Prod. 2003;66:423-6. (Pubitemid 36384025)
    • (2003) Journal of Natural Products , vol.66 , Issue.3 , pp. 423-426
    • Garo, E.1    Starks, C.M.2    Jensen, P.R.3    Fenical, W.4    Lobkovsky, E.5    Clardy, J.6
  • 138
    • 0034541340 scopus 로고    scopus 로고
    • Penicillazine, a unique quinolone derivative with 4H-5,6-dihydro-1,2- oxazine ring system from the marine fungus penicillium sp. (Strain 386) from the south China sea
    • Lin Y, Shao Z, Jiang G., Zhou S, et al Penicillazine, a unique quinolone derivative with 4H-5,6-dihydro-1,2-oxazine ring system from the marine fungus Penicillium sp. (Strain 386) from the South China Sea. Tetrahedron 2000;56:9607-9.
    • (2000) Tetrahedron , vol.56 , pp. 9607-9609
    • Lin, Y.1    Shao, Z.2    Jiang, G.3    Zhou, S.4
  • 139
    • 33947572492 scopus 로고    scopus 로고
    • Progress towards the total synthesis of trichodermamides A and B: Construction of the oxazine ring moiety
    • Wan XB, Doridot G, Joullie MM Progress towards the total synthesis of trichodermamides A and B: construction of the oxazine ring moiety. Org Lett. 2007;9(6):977-86.
    • (2007) Org Lett. , vol.9 , Issue.6 , pp. 977-986
    • Wan, X.B.1    Doridot, G.2    Joullie, M.M.3
  • 141
    • 0015155001 scopus 로고
    • Modification, permethylation, and mass spectrometry of arginine-containing oligopeptides at the 100 nanomolar level
    • Leclercq PA, Smith LC, Desiderio DM Jr. Modification, permethylation, and mass spectrometry of arginine-containing oligopeptides at the 100 nanomolar level. Biochem Biophys Res Commun. 1971;45:937-44.
    • (1971) Biochem Biophys Res Commun. , vol.45 , pp. 937-944
    • Leclercq, P.A.1    Smith, L.C.2    Desiderio Jr., D.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.