메뉴 건너뛰기




Volumn 8, Issue 12, 2010, Pages 2906-2935

Bioactive dehydrotyrosyl and dehydrodopyl compounds of marine origin

Author keywords

Bioactive peptides; Dehydrodopa; dehydrotopa; Dehydrotyrosine; Marine alkaloids

Indexed keywords

1,2 DEHYDRO N ACETYLDOPAMINE; BOTRYLLAMIDE; CLIONAMIDE; ERBSTATIN; HALITULIN; HYDROXYAMINO ACID; LEUCETTAMINE A; MORULIN PM; PLICATAMIDE; POLYANDROCARPAMINE A; RIGIDIN A; STORNIAMIDE A; TRIDENTATOL A; TRIDENTATOL B; TRIDENTATOL C; TRIDENTATOL D; TUBASTRINE; TUBERINE; TUNICHROME AN 1; TUNICHROME AN 2; TUNICHROME AN 3; TUNICHROME MM 1; TUNICHROME MM 2; TUNICHROME PM 1; TUNICHROME PM 2; TUNICHROME PM 3; TYROSINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; WONDONIN A; WONDONIN B;

EID: 78650673521     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md8122906     Document Type: Review
Times cited : (39)

References (115)
  • 2
    • 45949112254 scopus 로고    scopus 로고
    • Gram-negative antibiotic resistance: There is a price to pay
    • Slama, T.G. Gram-negative antibiotic resistance: There is a price to pay. Crit. Care 2008, 12, 1-7.
    • (2008) Crit. Care , vol.12 , pp. 1-7
    • Slama, T.G.1
  • 3
    • 65249146929 scopus 로고    scopus 로고
    • Multidrug resistance in bacteria
    • Nikaido, H. Multidrug resistance in bacteria. Annu. Rev. Biochem. 2009, 78, 119-146.
    • (2009) Annu. Rev. Biochem. , vol.78 , pp. 119-146
    • Nikaido, H.1
  • 6
    • 33645419340 scopus 로고    scopus 로고
    • René dubos: Unearthing antibiotics
    • Van Epps, H.L. René Dubos: Unearthing antibiotics. J. Exp. Med. 2006, 203, 259.
    • (2006) J. Exp. Med. , vol.203 , pp. 259
    • Van Epps, H.L.1
  • 7
    • 21344453544 scopus 로고    scopus 로고
    • Molecular phylogeny of the protochordates: Chordate evolution
    • Zeng, L.; Swalla, B.J. Molecular phylogeny of the protochordates: Chordate evolution. Can. J. Zool. 2005, 83, 24-33.
    • (2005) Can. J. Zool. , vol.83 , pp. 24-33
    • Zeng, L.1    Swalla, B.J.2
  • 8
    • 0034623953 scopus 로고    scopus 로고
    • Styelin D, an extensively modified antimicrobial peptide from ascidian hemocytes
    • Taylor, S.W.; Craig, A.F.; Fischer, W.H.; Park, M.; Lehrer, R.I. Styelin D, an extensively modified antimicrobial peptide from ascidian hemocytes. J. Biol. Chem. 2000, 275, 38417-38426.
    • (2000) J. Biol. Chem. , vol.275 , pp. 38417-38426
    • Taylor, S.W.1    Craig, A.F.2    Fischer, W.H.3    Park, M.4    Lehrer, R.I.5
  • 9
    • 0034643280 scopus 로고    scopus 로고
    • Plicatamide: A lead to the biosynthetic origins of the tunichromes
    • Tincu, J.A.; Craig, A.G.; Taylor, S.W. Plicatamide: A lead to the biosynthetic origins of the tunichromes. Biochem. Biophys. Res. Commun. 2000, 270, 421-424.
    • (2000) Biochem. Biophys. Res. Commun. , vol.270 , pp. 421-424
    • Tincu, J.A.1    Craig, A.G.2    Taylor, S.W.3
  • 10
    • 0025097969 scopus 로고
    • Halocyamines: Novel antibacterial tetrapeptide-like structures isolated from the hemocytes of the solitary ascidian halocynthia roretzi
    • Azumi, K.; Yokosawa, H.; Ishii, S. Halocyamines: Novel antibacterial tetrapeptide-like structures isolated from the hemocytes of the solitary ascidian halocynthia roretzi. Biochemistry 1990, 29, 159-165.
    • (1990) Biochemistry , vol.29 , pp. 159-165
    • Azumi, K.1    Yokosawa, H.2    Ishii, S.3
  • 11
    • 38749120651 scopus 로고    scopus 로고
    • Lamellarins and related pyrrole derived alkaloids from marine organisms
    • Fan, H.; Peng, J.; Hamann, M.T.; Hu, J.F. Lamellarins and related pyrrole derived alkaloids from marine organisms. Chem. Rev. 2008, 108, 264-287.
    • (2008) Chem. Rev. , vol.108 , pp. 264-287
    • Fan, H.1    Peng, J.2    Hamann, M.T.3    Hu, J.F.4
  • 12
    • 0000444745 scopus 로고
    • Ferreascidin: A highly aromatic protein containing 3,4- dihydroxypphenylalanine from the blood cells of a stolidobranch ascidian
    • Dorsett, L.C.; Hawkins, C.J.; Grice, J.A.; Lavin, M.F.; Merefield, P.M.; Parry, D.L.; Ross, I.L. Ferreascidin: A highly aromatic protein containing 3,4-dihydroxypphenylalanine from the blood cells of a stolidobranch ascidian. Biochemistry 1987, 26, 8078-8082.
    • (1987) Biochemistry , vol.26 , pp. 8078-8082
    • Dorsett, L.C.1    Hawkins, C.J.2    Grice, J.A.3    Lavin, M.F.4    Merefield, P.M.5    Parry, D.L.6    Ross, I.L.7
  • 13
    • 0018508886 scopus 로고
    • Isolation properties and structural studies on a compound from tunicate blood cells that may be involved in vanadium accumulation
    • Macara, I.G.; McLeod, G.C.; Kustin, K. Isolation, properties and structural studies on a compound from tunicate blood cells that may be involved in vanadium accumulation. Biochem. J. 1979, 181, 457-465.
    • (1979) Biochem. J. , vol.181 , pp. 457-465
    • MacAra, I.G.1    McLeod, G.C.2    Kustin, K.3
  • 14
    • 0000641503 scopus 로고
    • Isolation and structure of tunichrome B-1, a reducing blood pigment from the tunicate Ascidia nigra L
    • Bruening, R.C.; Oltz, E.M.; Furukawa, J.; Nakanishi, K. Isolation and structure of tunichrome B-1, a reducing blood pigment from the tunicate Ascidia nigra L. J. Am. Chem. Soc. 1985, 107, 5298-5300.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 5298-5300
    • Bruening, R.C.1    Oltz, E.M.2    Furukawa, J.3    Nakanishi, K.4
  • 15
    • 0022675662 scopus 로고
    • Isolation of tunichrome B-1, a reducing blood pigment of the sea squirt, Ascidia nigra
    • Bruening, R.C.; Oltz, E.M.; Furukawa, J.; Nakanishi, K.; Kustin, K. Isolation of tunichrome B-1, a reducing blood pigment of the sea squirt, Ascidia nigra. J. Nat. Prod. 1986, 49, 193-204.
    • (1986) J. Nat. Prod. , vol.49 , pp. 193-204
    • Bruening, R.C.1    Oltz, E.M.2    Furukawa, J.3    Nakanishi, K.4    Kustin, K.5
  • 16
    • 33845278462 scopus 로고
    • The tunichromes. A class of reducing blood pigments from sea squirts: Isolation, structures and vanadium chemistry
    • Oltz, E.M.; Bruening, R.C.; Smith, M.J.; Kustin, K.; Nakanishi, K. The tunichromes. A class of reducing blood pigments from sea squirts: Isolation, structures and vanadium chemistry. J. Am. Chem. Soc. 1988, 110, 6162-6172.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 6162-6172
    • Oltz, E.M.1    Bruening, R.C.2    Smith, M.J.3    Kustin, K.4    Nakanishi, K.5
  • 18
    • 0000170376 scopus 로고
    • Distribution of tunichromes in the Ascidiacea
    • Parry, D.L.; Brand, S.G.; Kustin, K. Distribution of tunichromes in the Ascidiacea. Bull. Mar. Sci. 1992, 50, 302-306.
    • (1992) Bull. Mar. Sci. , vol.50 , pp. 302-306
    • Parry, D.L.1    Brand, S.G.2    Kustin, K.3
  • 19
    • 0036201034 scopus 로고    scopus 로고
    • Tunichrome Sp-1: New pentapeptide tunichrome from the hemocytes of Styela plicata
    • Tincu, J.A.; Taylor, S.W. Tunichrome Sp-1: New pentapeptide tunichrome from the hemocytes of Styela plicata. J. Nat. Prod. 2002, 65, 377-378.
    • (2002) J. Nat. Prod. , vol.65 , pp. 377-378
    • Tincu, J.A.1    Taylor, S.W.2
  • 20
    • 78650660004 scopus 로고
    • A new antibiotic, tuberine, V: Biological activities of tuberine analogs
    • Okuma, K.; Anzai, S.; Suzuki, S. A new antibiotic, tuberine, V: Biological activities of tuberine analogs. J. Antibiot. 1962, 15, 202-209.
    • (1962) J. Antibiot. , vol.15 , pp. 202-209
    • Okuma, K.1    Anzai, S.2    Suzuki, S.3
  • 21
    • 0022630086 scopus 로고
    • Studies on a new epidermal growth factor-receptor kinase inhibitor, erbstatin, produced by MH435-hF3
    • Umezawa, H.; Imoto, M.; Sawa, T.; Isshiki, K.; Matsuda, N.; Uchida, T.; Iinuma, H.; Hamada, M.; Takeuchi, T. Studies on a new epidermal growth factor-receptor kinase inhibitor, erbstatin, produced by MH435-hF3. J. Antibiot. 1986, 39, 170-173. (Pubitemid 16174654)
    • (1986) Journal of Antibiotics , vol.39 , Issue.1 , pp. 170-173
    • Umezawa, H.1    Imoto, M.2    Sawa, T.3
  • 22
    • 0032946285 scopus 로고    scopus 로고
    • Isolation of p-hydroxycinnamaldehyde as an antibacterial substance from the saw fly, Acantholyda parki S
    • Leem, J.Y.; Jeong, I.M.; Park, K.T.; Park, H.Y. Isolation of p-hydroxycinnamaldehyde as an antibacterial substance from the saw fly, Acantholyda parki S. FEBS Lett. 1999, 442, 53-56.
    • (1999) FEBS Lett. , vol.442 , pp. 53-56
    • Leem, J.Y.1    Jeong, I.M.2    Park, K.T.3    Park, H.Y.4
  • 23
    • 0014486789 scopus 로고
    • Alcaloides peptidiques-VII. les lasiodines A et B alcoloides du Lasidiscus marmoratus. C.H. Wright (Rhamnacees)
    • Marchand, J.; Pais, M.; Monseur, X.; Jarreau, F.X. Alcaloides peptidiques-VII. Les lasiodines A et B, alcoloides du Lasidiscus marmoratus. C.H. Wright (Rhamnacees). Tetrahedron 1969, 25, 937-954.
    • (1969) Tetrahedron , vol.25 , pp. 937-954
    • Marchand, J.1    Pais, M.2    Monseur, X.3    Jarreau, F.X.4
  • 26
    • 75449084213 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of botryllamides that block the ABCG2 multidrug transporter
    • Takada, K.; Imamura, N.; Gustafson, K.R.; Henrich, C.J. Synthesis and structure-activity relationship of botryllamides that block the ABCG2 multidrug transporter. Bioorg. Med. Chem. Lett. 2010, 20, 1330-1333.
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 1330-1333
    • Takada, K.1    Imamura, N.2    Gustafson, K.R.3    Henrich, C.J.4
  • 27
    • 33645802552 scopus 로고    scopus 로고
    • New alkaloids from the Mediterranean sponge, Hamigera hamigera
    • Hassan, W.; Edrada, R.; Ebel, R.; Wray, V.; Proksch, P. New alkaloids from the Mediterranean sponge, Hamigera hamigera. Mar. Drugs 2004, 2, 88-100.
    • (2004) Mar. Drugs , vol.2 , pp. 88-100
    • Hassan, W.1    Edrada, R.2    Ebel, R.3    Wray, V.4    Proksch, P.5
  • 28
    • 0030590968 scopus 로고    scopus 로고
    • Tridentatols A-C novel natural products of the marine hydroid Tridentata marginata
    • Lindquist, N.; Lobkovsky, E.; Clardy, J. Tridentatols A-C, novel natural products of the marine hydroid Tridentata marginata. Tetrahedron Lett. 1996, 37, 9131-9134.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 9131-9134
    • Lindquist, N.1    Lobkovsky, E.2    Clardy, J.3
  • 29
    • 0032839675 scopus 로고    scopus 로고
    • Potent antioxidant activity of a dithiocarbamate related compound from a marine hydroid
    • Johnson, M.K.; Alexander, K.E.; Lindquist, N.; Loo, G. Potent antioxidant activity of a dithiocarbamate related compound from a marine hydroid. Biochem. Pharmacol. 1999, 58, 1313-1319.
    • (1999) Biochem. Pharmacol. , vol.58 , pp. 1313-1319
    • Johnson, M.K.1    Alexander, K.E.2    Lindquist, N.3    Loo, G.4
  • 30
    • 0030931909 scopus 로고    scopus 로고
    • Chemical defense among hydroids on pelagic Sargassum: Predator deterrence and absorption of solar UV radiation by secondary metabolites
    • Stachowicz, J.J.; Lindquist, N. Chemical defense among hydroids on pelagic Sargassum: Predator deterrence and absorption of solar UV radiation by secondary metabolites. Mar. Ecol. Prog. Ser. 1997, 155, 115-126.
    • (1997) Mar. Ecol. Prog. Ser. , vol.155 , pp. 115-126
    • Stachowicz, J.J.1    Lindquist, N.2
  • 31
    • 0036112487 scopus 로고    scopus 로고
    • Tridentatols D-H nematocyst metabolites and precursors of the activated chemical defense in the marine hydroid Tridentata marginata (Kirchenpauer 1864)
    • Lindquist, N. Tridentatols D-H, nematocyst metabolites and precursors of the activated chemical defense in the marine hydroid Tridentata marginata (Kirchenpauer 1864). J. Nat. Prod. 2002, 65, 681-684.
    • (2002) J. Nat. Prod. , vol.65 , pp. 681-684
    • Lindquist, N.1
  • 32
    • 0029079505 scopus 로고
    • Pipecolate derivates, anthosamines A and B inducers of larval metamorphosis in ascidians, from a marine sponge, Anthosigmella aff. raromicrosclera
    • Tsukamoto, S.; Kato, H.; Hirota, H.; Fusetani, N. Pipecolate derivates, anthosamines A and B inducers of larval metamorphosis in ascidians, from a marine sponge, Anthosigmella aff. raromicrosclera. Tetrahedron 1995, 51, 6687-6694.
    • (1995) Tetrahedron , vol.51 , pp. 6687-6694
    • Tsukamoto, S.1    Kato, H.2    Hirota, H.3    Fusetani, N.4
  • 33
    • 0025345419 scopus 로고
    • Rigidin a novel alkaloid with calmodulin antagonistic activity from the okinawan marine tunicate Eudistoma cf rigida
    • Kobayashi, J.; Cheng, J.F.; Kikuchi, Y.; Ishibashi, M.; Yamamura, S.; Ohizumi, Y.; Ohta, T.; Nozoe, S. Rigidin, a novel alkaloid with calmodulin antagonistic activity from the okinawan marine tunicate Eudistoma cf. rigida. Tetrahedron Lett. 1990, 31, 4617-4620.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 4617-4620
    • Kobayashi, J.1    Cheng, J.F.2    Kikuchi, Y.3    Ishibashi, M.4    Yamamura, S.5    Ohizumi, Y.6    Ohta, T.7    Nozoe, S.8
  • 34
    • 0037332091 scopus 로고    scopus 로고
    • Rigidins B-D New pyrrolopyrimidine alkaloids from a tunicate Cystodytes species
    • Tsuda, M.; Nozawa, K.; Shimbo, K.; Kobayashi, J. Rigidins B-D, New pyrrolopyrimidine alkaloids from a tunicate Cystodytes species. J. Nat. Prod. 2003, 66, 292-294.
    • (2003) J. Nat. Prod. , vol.66 , pp. 292-294
    • Tsuda, M.1    Nozawa, K.2    Shimbo, K.3    Kobayashi, J.4
  • 35
    • 0002240694 scopus 로고
    • Sclerotization of insect cuticle-II Isolation and identification of phenolic dimers from sclerotized insect cuticle
    • Andersen, S.O.; Roepstorff, P. Sclerotization of insect cuticle-II Isolation and identification of phenolic dimers from sclerotized insect cuticle. Insect Biochem. 1981, 11, 25-31.
    • (1981) Insect Biochem. , vol.11 , pp. 25-31
    • Andersen, S.O.1    Roepstorff, P.2
  • 36
    • 0019164987 scopus 로고
    • Studies of the sclerotization of insect cuticle-The structure of dimeric products formed by incubation of N-acetyldopamine with locust cuticle
    • Andersen, S.O.; Jacobsen, J.P.; Roepstorff, P. Studies of the sclerotization of insect cuticle-The structure of dimeric products formed by incubation of N-acetyldopamine with locust cuticle. Tetrahedron 1980, 36, 3249-3252.
    • (1980) Tetrahedron , vol.36 , pp. 3249-3252
    • Andersen, S.O.1    Jacobsen, J.P.2    Roepstorff, P.3
  • 37
    • 49049136604 scopus 로고
    • Sclerotization of insect cuticle-III. An unsaturated derivative of N-acetyldopamine and its role in sclerotization
    • Andersen, S.O.; Roepstorff, P. Sclerotization of insect cuticle-III. An unsaturated derivative of N-acetyldopamine and its role in sclerotization. Insect Biochem. 1982, 12, 269-276.
    • (1982) Insect Biochem. , vol.12 , pp. 269-276
    • Andersen, S.O.1    Roepstorff, P.2
  • 38
    • 0023645278 scopus 로고
    • Tyrosinase catalyzed unusual oxidative dimerization of 1,2-dehydro-N-acetyldopamine
    • Sugumaran, M.; Dali, H.; Semensi, V.; Hennigan, B. Tyrosinase catalyzed unusual oxidative dimerization of 1,2-dehydro-N-acetyldopamine. J. Biol. Chem. 1987, 262, 10546-10549.
    • (1987) J. Biol. Chem. , vol.262 , pp. 10546-10549
    • Sugumaran, M.1    Dali, H.2    Semensi, V.3    Hennigan, B.4
  • 39
    • 84990485091 scopus 로고
    • On the nature of nonenzymatic and enzymatic oxidation of the putative sclerotizing precursor, 1,2-dehydro-N-acetyldopamine
    • Sugumaran, M.; Hennigan, B.; Semensi, V.; Dali, H. On the nature of nonenzymatic and enzymatic oxidation of the putative sclerotizing precursor, 1,2-dehydro-N-acetyldopamine. Arch. Insect Biochem. Physiol. 1988, 8, 89-100.
    • (1988) Arch. Insect Biochem. Physiol. , vol.8 , pp. 89-100
    • Sugumaran, M.1    Hennigan, B.2    Semensi, V.3    Dali, H.4
  • 41
    • 0026727777 scopus 로고
    • Evidence for the formation of a quinone methide during the oxidation of the insect cuticular sclerotizing precursor, 1,2-dehydro-N-acetyldopamine
    • Sugumaran, M.; Semensi, V.; Kalyanaraman, B.; Bruce, J.M.; Land, E.J. Evidence for the formation of a quinone methide during the oxidation of the insect cuticular sclerotizing precursor, 1,2-dehydro-N-acetyldopamine. J. Biol. Chem. 1992, 267, 10355-10361.
    • (1992) J. Biol. Chem. , vol.267 , pp. 10355-10361
    • Sugumaran, M.1    Semensi, V.2    Kalyanaraman, B.3    Bruce, J.M.4    Land, E.J.5
  • 42
    • 0034660346 scopus 로고    scopus 로고
    • Oxidation chemistry of 1,2-dehydro-N-acetyldopamines: Direct evidence for the formation of 1,2-dehydro-N-acetyldopamine quinone
    • Sugumaran, M. Oxidation chemistry of 1,2-dehydro-N-acetyldopamines: Direct evidence for the formation of 1,2-dehydro-N-acetyldopamine quinone. Arch. Biochem. Biophys. 2000, 378, 404-410.
    • (2000) Arch. Biochem. Biophys. , vol.378 , pp. 404-410
    • Sugumaran, M.1
  • 43
    • 77956182067 scopus 로고    scopus 로고
    • Reexamination of the mechanisms of oxidative transformations of the insect cuticular sclerotization precursor, 1,2-dehydro-N-acetyldopamine
    • Abebe, A.; Zheng, D.; Evans, J.; Sugumaran, M. Reexamination of the mechanisms of oxidative transformations of the insect cuticular sclerotization precursor, 1,2-dehydro-N-acetyldopamine. Insect Biochem. Mol. Biol. 2010, 40, 650-659.
    • (2010) Insect Biochem. Mol. Biol. , vol.40 , pp. 650-659
    • Abebe, A.1    Zheng, D.2    Evans, J.3    Sugumaran, M.4
  • 44
    • 77956736927 scopus 로고    scopus 로고
    • Unified mechanism for sclerotization of insect cuticle
    • Sugumaran, M. Unified mechanism for sclerotization of insect cuticle. Adv. Insect Physiol. 1998, 27, 229-334.
    • (1998) Adv. Insect Physiol. , vol.27 , pp. 229-334
    • Sugumaran, M.1
  • 45
    • 77957963448 scopus 로고    scopus 로고
    • Chemistry of cuticular sclerotization
    • Sugumaran, M. Chemistry of cuticular sclerotization. Adv. Insect Physiol. 2010, 39, 151-209.
    • (2010) Adv. Insect Physiol. , vol.39 , pp. 151-209
    • Sugumaran, M.1
  • 46
    • 0033672526 scopus 로고    scopus 로고
    • Optically active N-acetyldopamine dimer of the crude drug ?Zentai?, the cast-off shell of the Cicada Cryptotympana sp
    • Noda, N.; Kubota, S.; Miyata, Y.; Miyahara, K. Optically active N-acetyldopamine dimer of the crude drug ?Zentai?, the cast-off shell of the Cicada Cryptotympana sp. Chem. Pharm. Bull. 2000, 48, 1749-1752.
    • (2000) Chem. Pharm. Bull. , vol.48 , pp. 1749-1752
    • Noda, N.1    Kubota, S.2    Miyata, Y.3    Miyahara, K.4
  • 47
    • 77956191420 scopus 로고    scopus 로고
    • Potential cosmetic whitening agents from insect cuticle: Tyrosinase inhibitory activity of N-acetyldopamine dimers from the exuviae of Cicada, Cryptotympana tuslulata FABR
    • Tada, T.; Ohnishi, K.; Suzuki, K.; Tomita, H.; Okamori, M.; Katuzaki, H.; Komiya, T.; Imai, K. Potential cosmetic whitening agents from insect cuticle: Tyrosinase inhibitory activity of N-acetyldopamine dimers from the exuviae of Cicada, Cryptotympana tuslulata FABR. J. Oleo Sci. 2002, 51, 355-358.
    • (2002) J. Oleo Sci. , vol.51 , pp. 355-358
    • Tada, T.1    Ohnishi, K.2    Suzuki, K.3    Tomita, H.4    Okamori, M.5    Katuzaki, H.6    Komiya, T.7    Imai, K.8
  • 48
    • 33750064866 scopus 로고    scopus 로고
    • Antioxidant and anti-inflammatory activities of N-acetyldopamine dimers from periostracum Cicadae
    • Xu, M.Z.; Lee, W.S.; Han, J.M.; Oh, H.W.; Park, D.S.; Tian, G.R.; Jeong, T.S.; Park, H.Y. Antioxidant and anti-inflammatory activities of N-acetyldopamine dimers from periostracum Cicadae. Bioorg. Med. Chem. 2006, 14, 7826-7834.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 7826-7834
    • Xu, M.Z.1    Lee, W.S.2    Han, J.M.3    Oh, H.W.4    Park, D.S.5    Tian, G.R.6    Jeong, T.S.7    Park, H.Y.8
  • 49
    • 0003140821 scopus 로고
    • Tubastrine a new guanidinostyrene from the coral Tubastrea aurea
    • Sakai, R.; Higa, T. Tubastrine, a new guanidinostyrene from the coral Tubastrea aurea. Chem. Lett. 1987, 127-128.
    • (1987) Chem. Lett. , pp. 127-128
    • Sakai, R.1    Higa, T.2
  • 50
    • 0031818218 scopus 로고    scopus 로고
    • Dihydrotubastrines: Phenethylguanidine analogues from the Indo-Pacific marine sponge, Petrosia cf contignata
    • Sperry, S.; Crews, P. Dihydrotubastrines: phenethylguanidine analogues from the Indo-Pacific marine sponge, Petrosia cf. contignata. J. Nat. Prod. 1998, 61, 859-861.
    • (1998) J. Nat. Prod. , vol.61 , pp. 859-861
    • Sperry, S.1    Crews, P.2
  • 51
    • 18144415094 scopus 로고    scopus 로고
    • Screening enzyme-inhibitory activity in several ascidian species from Orkney Islands using protein tyrosine kinase (PTK) bioassay-guided fractionation
    • Barenbrock, J.S.; Kock, M. Screening enzyme-inhibitory activity in several ascidian species from Orkney Islands using protein tyrosine kinase (PTK) bioassay-guided fractionation. J. Biotechnol. 2005, 117, 225-232.
    • (2005) J. Biotechnol. , vol.117 , pp. 225-232
    • Barenbrock, J.S.1    Kock, M.2
  • 52
    • 43449099138 scopus 로고    scopus 로고
    • Orthidines A-E tubastrine, 3,4-dimethoxyphenylethyl-b-guanidine, and 1,14-sperminedihomovanillamide: Potential anti-inflammatory alkaloids isolated from the New Zealand ascidian Aplidium orthium that act as inhibitors of neutrophil respiratory burst
    • Pearce, A.N.; Chia, E.W.; Berridge, M.V.; Maas, E.W.; Page, M.J.; Harper, J.L.; Webb, V.L.; Copp, B.R. Orthidines A-E, tubastrine, 3,4- dimethoxyphenylethyl-b-guanidine, and 1,14-sperminedihomovanillamide: Potential anti-inflammatory alkaloids isolated from the New Zealand ascidian Aplidium orthium that act as inhibitors of neutrophil respiratory burst. Tetrahedron 2008, 64, 5748-5755.
    • (2008) Tetrahedron , vol.64 , pp. 5748-5755
    • Pearce, A.N.1    Chia, E.W.2    Berridge, M.V.3    Maas, E.W.4    Page, M.J.5    Harper, J.L.6    Webb, V.L.7    Copp, B.R.8
  • 53
    • 0000293038 scopus 로고
    • Jaspisin a novel styryl sulfate from the marine sponge, Jaspis species
    • Ohta, S.; Kobayashi, H.; Ikegami, S. Jaspisin, a novel styryl sulfate from the marine sponge, Jaspis species. Biosci. Biotechnol. Biochem. 1994, 58, 1752-1753.
    • (1994) Biosci. Biotechnol. Biochem. , vol.58 , pp. 1752-1753
    • Ohta, S.1    Kobayashi, H.2    Ikegami, S.3
  • 54
    • 0028272318 scopus 로고
    • Isojaspisin a novel styryl sulfate from a marine sponge, Jaspis sp., that inhibits hatching of sea urchin embryos
    • Ohta, S.; Kobayashi, H.; Ikegami, S. Isojaspisin, a novel styryl sulfate from a marine sponge, Jaspis sp., that inhibits hatching of sea urchin embryos. Tetrahedron Lett. 1994, 35, 4579-4580.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4579-4580
    • Ohta, S.1    Kobayashi, H.2    Ikegami, S.3
  • 55
    • 0028021743 scopus 로고
    • Selective inhibition of exoplasmic membrane fusion in echinoderm gametes with jaspisin, a novel antihatching substance isolated from a marine sponge
    • Ikegami, S.; Kobayashi, H.; Myotoishi, Y.; Ohta, S.; Kato, K.H. Selective inhibition of exoplasmic membrane fusion in echinoderm gametes with jaspisin, a novel antihatching substance isolated from a marine sponge. J. Biol. Chem. 1994, 269, 23262-23267.
    • (1994) J. Biol. Chem. , vol.269 , pp. 23262-23267
    • Ikegami, S.1    Kobayashi, H.2    Myotoishi, Y.3    Ohta, S.4    Kato, K.H.5
  • 56
    • 0028064418 scopus 로고
    • Narains: N, N-dimethylguanidinium styryl sulfates, metamorphosis inducers of ascidian larvae from a marine sponge, Jaspis sp
    • Tsukamoto, B.; Kato, H.; Hirota, H.; Fusetani, N. Narains: N,N-dimethylguanidinium styryl sulfates, metamorphosis inducers of ascidian larvae from a marine sponge, Jaspis sp. Tetrahedron Lett. 1994, 35, 5874-5874.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 5874-5874
    • Tsukamoto, B.1    Kato, H.2    Hirota, H.3    Fusetani, N.4
  • 57
    • 0028149744 scopus 로고
    • 3,4-Dihydroxystyrene dimers, inducers of larval metamorphosis in ascidians, from a marine sponge Jaspis sp.
    • DOI 10.1016/S0040-4020(01)85673-8
    • Tsukamoto, B.; Kato, H.; Hirota, H.; Fusetani, N. 3,4-Dihydroxystyrene dimers, inducers of larval metamorphosis in ascidians, from a marine sponge, Jaspis sp. Tetrahedron 1994, 48, 13583-13592. (Pubitemid 24355269)
    • (1994) Tetrahedron , vol.50 , Issue.48 , pp. 13583-13592
    • Tsukamoto, S.1    Kato, H.2    Hirota, H.3    Fusetani, N.4
  • 58
    • 0035804481 scopus 로고    scopus 로고
    • Wondonins A and B, new bis(dihydroxystyryl)imidazoles from a two sponge association
    • Shin, J.; Rho, J.R.; Seo, Y.; Lee, H.S.; Cho, K.W.; Kwon, H.J.; Sim, C.J. Wondonins A and B, new bis(dihydroxystyryl)imidazoles from a two sponge association. Tetrahedron Lett. 2001, 42, 1965-1968.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 1965-1968
    • Shin, J.1    Rho, J.R.2    Seo, Y.3    Lee, H.S.4    Cho, K.W.5    Kwon, H.J.6    Sim, C.J.7
  • 59
    • 0027348616 scopus 로고
    • New leukotriene B4 receptor antagonist: Leucettamine A and related imidazoles alkaloids from the marine sponge, Leucetta microraphis
    • Chan, G.W.; Mong, S.; Hemling, M.E.; Freyer, A.J.; Offen, P.H.; DeBrosse, C.W., Sarau, H.M.; Westley, J.W. New leukotriene B4 receptor antagonist: Leucettamine A and related imidazoles alkaloids from the marine sponge, Leucetta microraphis. J. Nat. Prod. 1993, 56, 116-121.
    • (1993) J. Nat. Prod. , vol.56 , pp. 116-121
    • Chan, G.W.1    Mong, S.2    Hemling, M.E.3    Freyer, A.J.4    Offen, P.H.5    Debrosse, C.W.6    Sarau, H.M.7    Westley, J.W.8
  • 60
    • 0037332293 scopus 로고    scopus 로고
    • Variation in the alkaloids among Indo-Pacific Leucetta sponges
    • Crews, P.; Clark, D.P.; Tenney, K. Variation in the alkaloids among Indo-Pacific Leucetta sponges. J. Nat. Prod. 2003, 66, 177-182.
    • (2003) J. Nat. Prod. , vol.66 , pp. 177-182
    • Crews, P.1    Clark, D.P.2    Tenney, K.3
  • 61
    • 73849133993 scopus 로고    scopus 로고
    • Synthesis and preliminary biological evaluation of new derivatives of the marine alkaloid leucettamine B as kinase inhibitors
    • Debdab, M.; Renault, S.; Lozach, O.; Meijer, L.; Paquin, L.; Carreaux, F.; Bazuraeu, J.P. Synthesis and preliminary biological evaluation of new derivatives of the marine alkaloid leucettamine B as kinase inhibitors. Eur. J. Med. Chem. 2010, 45, 805-810.
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 805-810
    • Debdab, M.1    Renault, S.2    Lozach, O.3    Meijer, L.4    Paquin, L.5    Carreaux, F.6    Bazuraeu, J.P.7
  • 62
    • 0037090557 scopus 로고    scopus 로고
    • The isolation and synthesis of polyandrocarpamines A and B. Two new 2-aminoimidazolone compounds from the Fijian ascidian, Polyandrocarpa sp
    • Davis, R.A.; Aalbersberg, W.; Meo, S.; Moreira da Rocha, R.; Ireland, C.M. The isolation and synthesis of polyandrocarpamines A and B. Two new 2-aminoimidazolone compounds from the Fijian ascidian, Polyandrocarpa sp. Tetrahedron 2002, 58, 3263-3269.
    • (2002) Tetrahedron , vol.58 , pp. 3263-3269
    • Davis, R.A.1    Aalbersberg, W.2    Meo, S.3    Moreira Da Rocha, R.4    Ireland, C.M.5
  • 63
    • 58149354129 scopus 로고    scopus 로고
    • A microwave-assisted stereoselective synthesis of polyandrocarpamines A and B
    • Davis, R.A.; Baron, P.S.; Neve, J.E.; Cullinane, C. A microwave-assisted stereoselective synthesis of polyandrocarpamines A and B. Tetrahedron Lett. 2009, 50, 880-882.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 880-882
    • Davis, R.A.1    Baron, P.S.2    Neve, J.E.3    Cullinane, C.4
  • 64
    • 0018711065 scopus 로고
    • Clionamide a major metabolite of the sponge Cliona celata Grant
    • Andersen, R.J.; Stonard, R.J. Clionamide, a major metabolite of the sponge Cliona celata Grant. Can. J. Chem. 1979, 57, 2325-2328.
    • (1979) Can. J. Chem. , vol.57 , pp. 2325-2328
    • Andersen, R.J.1    Stonard, R.J.2
  • 65
  • 67
    • 4644311383 scopus 로고    scopus 로고
    • Antimicrobial peptides from marine invertebrates
    • Tincu, J.A.; Taylor, S.W. Antimicrobial peptides from marine invertebrates. Antimicrob. Agents Chemother. 2004, 48, 3645-3654.
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 3645-3654
    • Tincu, J.A.1    Taylor, S.W.2
  • 68
    • 0025135257 scopus 로고
    • Inhibitory effect of halocyamine, an antimicrobial substance from ascidian hemocytes, on the growth of fish viruses and marine bacteria
    • Azumi, K.; Yoshimizu, M.; Suzuki, S.; Ezura, Y.; Yokosawa, H. Inhibitory effect of halocyamine, an antimicrobial substance from ascidian hemocytes, on the growth of fish viruses and marine bacteria. Experientia 1990, 46, 1066-1068.
    • (1990) Experientia , vol.46 , pp. 1066-1068
    • Azumi, K.1    Yoshimizu, M.2    Suzuki, S.3    Ezura, Y.4    Yokosawa, H.5
  • 69
    • 33847085333 scopus 로고
    • Celenamides A and B linear peptide alkaloids from the sponge Cliona celala
    • Stonard, R.J.; Andersen, R.J. Celenamides A and B linear peptide alkaloids from the sponge Cliona celala. J. Org. Chem. 1980, 45, 3687-3691.
    • (1980) J. Org. Chem. , vol.45 , pp. 3687-3691
    • Stonard, R.J.1    Andersen, R.J.2
  • 70
    • 0001255796 scopus 로고
    • Linear peptide alkaloids from the sponge Cliona celata (Grant). Celenamides C and D
    • Stonard, R.J.; Andersen, R.J. Linear peptide alkaloids from the sponge Cliona celata (Grant). Celenamides C and D. Can. J. Chem. 1980, 58, 2121-2126.
    • (1980) Can. J. Chem. , vol.58 , pp. 2121-2126
    • Stonard, R.J.1    Andersen, R.J.2
  • 71
    • 0031968496 scopus 로고    scopus 로고
    • Celenamide e a tripeptide alkaloid from the Patagonian sponge Cliona chilensis
    • Palermo, J.A.; Brasco, M.F.R.; Cabezas, E.; Balzaretti, V.; Seldes, A.M. Celenamide E, a tripeptide alkaloid from the Patagonian sponge Cliona chilensis. J. Nat. Prod. 1998, 61, 488-490.
    • (1998) J. Nat. Prod. , vol.61 , pp. 488-490
    • Palermo, J.A.1    Brasco, M.F.R.2    Cabezas, E.3    Balzaretti, V.4    Seldes, A.M.5
  • 72
    • 1842373858 scopus 로고    scopus 로고
    • Effects of pH and salinity on the antimicrobial properties of clavanins
    • Lee, I.H.; Cho, Y.; Lehrer, R.I. Effects of pH and salinity on the antimicrobial properties of clavanins. Infect. Immun. 1997, 65, 2898-2903.
    • (1997) Infect. Immun. , vol.65 , pp. 2898-2903
    • Lee, I.H.1    Cho, Y.2    Lehrer, R.I.3
  • 74
    • 0037968647 scopus 로고    scopus 로고
    • Plicatamide an antimicrobial octapeptide from Styela plicata hemocytes
    • Lehrer, R.I. Plicatamide, an antimicrobial octapeptide from Styela plicata hemocytes. J. Biol. Chem. 2003, 278, 13546-13553.
    • (2003) J. Biol. Chem. , vol.278 , pp. 13546-13553
    • Lehrer, R.I.1
  • 75
    • 0035057952 scopus 로고    scopus 로고
    • Clavanins and styelins, alpha-helical antimicrobial peptides from the hemocytes of Styela clava
    • Lehrer, R.I.; Lee, I.H.; Menzel, L.; Waring, A.; Zhao, C. Clavanins and styelins, alpha-helical antimicrobial peptides from the hemocytes of Styela clava. Adv. Exp. Med. Biol. 2001, 484, 71-76.
    • (2001) Adv. Exp. Med. Biol. , vol.484 , pp. 71-76
    • Lehrer, R.I.1    Lee, I.H.2    Menzel, L.3    Waring, A.4    Zhao, C.5
  • 76
    • 0042203502 scopus 로고    scopus 로고
    • Natural peptide antibiotics from tunicates: Structures, functions and potential uses
    • Lehrer, R.I.; Tincu, J.A.; Taylor, S.W.; Menzel, L.P.; Waring, A.J. Natural peptide antibiotics from tunicates: Structures, functions and potential uses. Integr. Comp. Biol. 2003, 43, 313-322.
    • (2003) Integr. Comp. Biol. , vol.43 , pp. 313-322
    • Lehrer, R.I.1    Tincu, J.A.2    Taylor, S.W.3    Menzel, L.P.4    Waring, A.J.5
  • 77
    • 0029560564 scopus 로고
    • Novel 34-di- and 345-trihydroxyphenylalanine containing polypeptides from the blood cells of the ascidians Ascidia ceratodes and Molgula manhattensis
    • Taylor, S.W.; Ross, M.M.; Waite, H.J. Novel 3,4-di- and 3,4,5-trihydroxyphenylalanine containing polypeptides from the blood cells of the ascidians Ascidia ceratodes and Molgula manhattensis. Arch. Biochem. Biophys. 1995, 324, 228-240.
    • (1995) Arch. Biochem. Biophys. , vol.324 , pp. 228-240
    • Taylor, S.W.1    Ross, M.M.2    Waite, H.J.3
  • 81
    • 0001246667 scopus 로고    scopus 로고
    • New perspectives in the chemistry and biochemistry of the tunichromes and related compounds
    • Taylor, S.W.; Kammerer, B.; Bayer, E. New perspectives in the chemistry and biochemistry of the tunichromes and related compounds. Chem. Rev. 1997, 97, 333-346.
    • (1997) Chem. Rev. , vol.97 , pp. 333-346
    • Taylor, S.W.1    Kammerer, B.2    Bayer, E.3
  • 82
    • 0000029691 scopus 로고
    • The accumulation and distribution of vanadium, iron, and manganese in some solitary ascidians
    • Michibata, H.; Terada, T.; Anada, N.; Yamakawa, K.; Numakunai, T. The accumulation and distribution of vanadium, iron, and manganese in some solitary ascidians. Biol. Bull. 1986, 171, 672-681.
    • (1986) Biol. Bull. , vol.171 , pp. 672-681
    • Michibata, H.1    Terada, T.2    Anada, N.3    Yamakawa, K.4    Numakunai, T.5
  • 83
    • 0000342247 scopus 로고
    • Tunichromes vanadium, and vacuolated blood cells in tunicates
    • Kustin K.; Robinson W.E.; Smith, M.J. Tunichromes, vanadium, and vacuolated blood cells in tunicates. Invert. Reprod. Develop. 1990, 17, 129-139.
    • (1990) Invert. Reprod. Develop. , vol.17 , pp. 129-139
    • Kustin, K.1    Robinson, W.E.2    Smith, M.J.3
  • 84
    • 0021099316 scopus 로고
    • Evidence for a repeating 3,4-dihydroxyphenylalanine- and hydroxyproline-containing decapeptide in the adhesive protein of the mussel, Mytilus edulis L
    • Waite, H.J. Evidence for a repeating 3,4-dihydroxyphenylalanine- and hydroxyproline-containing decapeptide in the adhesive protein of the mussel, Mytilus edulis L. J. Biol. Chem. 1983, 258, 2911-2915.
    • (1983) J. Biol. Chem. , vol.258 , pp. 2911-2915
    • Waite, H.J.1
  • 85
    • 0023139072 scopus 로고
    • Nature's underwater adhesive specialist
    • Waite, H.J. Nature's underwater adhesive specialist. Int. J. Adhes. Adhes. 1987, 7, 9-14.
    • (1987) Int. J. Adhes. Adhes. , vol.7 , pp. 9-14
    • Waite, H.J.1
  • 86
    • 0025160176 scopus 로고
    • The phylogeny and chemical diversity of quinone tanned glues and varnishes
    • Waite, H.J. The phylogeny and chemical diversity of quinone tanned glues and varnishes. Comp. Biochem. Physiol. B 1990, 97, 19-29.
    • (1990) Comp. Biochem. Physiol. B , vol.97 , pp. 19-29
    • Waite, H.J.1
  • 87
    • 0033613698 scopus 로고    scopus 로고
    • Halitulin a new cytotoxic alkaloid from the marine sponge, Haliclona tulearensis
    • Kashman, Y.; Koren-Goldshlager, G.; Gravalos, M.D.G.; Schleyer, M. Halitulin, a new cytotoxic alkaloid from the marine sponge, Haliclona tulearensis. Tetrahedron Lett. 1999, 40, 997-1000.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 997-1000
    • Kashman, Y.1    Koren-Goldshlager, G.2    Gravalos, M.D.G.3    Schleyer, M.4
  • 88
    • 0343058970 scopus 로고    scopus 로고
    • Storniamides A-D: Alkaloids from a Patagonian Sponge Cliona sp
    • Palermo, J.A.; Brasco, M.F.R.; Seldes, A.M. Storniamides A-D: Alkaloids from a Patagonian Sponge Cliona sp. Tetrahedron 1996, 52, 2727-2734.
    • (1996) Tetrahedron , vol.52 , pp. 2727-2734
    • Palermo, J.A.1    Brasco, M.F.R.2    Seldes, A.M.3
  • 89
    • 0033550480 scopus 로고    scopus 로고
    • Total syntheses of ningalin a, lamellarin o, lukianol a, and permethyl storniamide a utilizing heterocyclic azadiene diels-alder reactions
    • Boger, D.; Boyce, C.; Labroli, M.; Sehon, C.; Jin, Q. 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.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 54-62
    • Boger, D.1    Boyce, C.2    Labroli, M.3    Sehon, C.4    Jin, Q.5
  • 90
    • 0037025916 scopus 로고    scopus 로고
    • Efficient relay syntheses and assessment of the DNA-cleaving properties of the pyrrole alkaloid derivatives permethyl storniamide A, lycogalic acid A dimethyl ester, and the halitulin core
    • Furstner, A.; Krause, H.; Thiel, O. Efficient relay syntheses and assessment of the DNA-cleaving properties of the pyrrole alkaloid derivatives permethyl storniamide A, lycogalic acid A dimethyl ester, and the halitulin core. Tetrahedron 2002, 58, 6373-6380.
    • (2002) Tetrahedron , vol.58 , pp. 6373-6380
    • Furstner, A.1    Krause, H.2    Thiel, O.3
  • 92
    • 56249133515 scopus 로고    scopus 로고
    • Antioxidant alkaloid from the South China sea marine sponge, Iotrochota sp
    • Liu, Y.; Ji, H.; Dong, J.; Zhang, S.; Lee, K.J.; Mathew, S. Antioxidant alkaloid from the South China sea marine sponge, Iotrochota sp. Z. Naturforsch. C 2008, 63, 636-638.
    • (2008) Z. Naturforsch. C , vol.63 , pp. 636-638
    • Liu, Y.1    Ji, H.2    Dong, J.3    Zhang, S.4    Lee, K.J.5    Mathew, S.6
  • 93
    • 0030906198 scopus 로고    scopus 로고
    • Ningalins A-D: Novel aromatic alkaloids from a Western Australian ascidian of the genus Didemnum
    • DOI 10.1021/jo962132+
    • Kang, H.; Fenical, W. Ningalins A-D: Novel aromatic alkaloids from a western Australian ascidian of the genus Didemnum. J. Org. Chem. 1997, 62, 3254-3262. (Pubitemid 27273267)
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.10 , pp. 3254-3262
    • Kang, H.1    Fenical, W.2
  • 94
    • 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
    • Boger, D.L.; Soenen, D.R.; Boyce, C.W.; Hedrick, M.P.; Jin, Q. 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, 2479-2483.
    • (2000) J. Org. Chem. , vol.65 , pp. 2479-2483
    • Boger, D.L.1    Soenen, D.R.2    Boyce, C.W.3    Hedrick, M.P.4    Jin, Q.5
  • 95
    • 8844241601 scopus 로고    scopus 로고
    • Multidrug resistance reversal activity of permethyl ningalin B amide derivatives
    • Tao, H.; Hwang, I.; Boger, D.L. Multidrug resistance reversal activity of permethyl ningalin B amide derivatives. Bioorg. Med. Chem. Lett. 2004, 14, 5979-5981.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 5979-5981
    • Tao, H.1    Hwang, I.2    Boger, D.L.3
  • 96
    • 77955418722 scopus 로고    scopus 로고
    • Baculiferins A-O, O-sulfated pyrrole alkaloids with anti-HIV-1 activity, from the Chinese marine sponge, Iotrochota Baculifera
    • Fan, H.; Li, Z.; Shen, S.; Zeng, Y.; Yang, Y.; Xu, M.; Bruhn, T.; Nhrun, H.; Morschhauser, J.; Bringmann, G.; Lin, W. Baculiferins A-O, O-sulfated pyrrole alkaloids with anti-HIV-1 activity, from the Chinese marine sponge, Iotrochota Baculifera. Bioorg. Med. Chem. 2010, 18, 5466-5474.
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 5466-5474
    • Fan, H.1    Li, Z.2    Shen, S.3    Zeng, Y.4    Yang, Y.5    Xu, M.6    Bruhn, T.7    Nhrun, H.8    Morschhauser, J.9    Bringmann, G.10    Lin, W.11
  • 98
    • 0000907439 scopus 로고
    • Clardy New alkaloids of the lamellarin class from the marine ascidian, Didemnum chartaceum (Sluiter, 1909)
    • Lindquist, N.; Fenical, W.; Van Duyne, G.D. Clardy, New alkaloids of the lamellarin class from the marine ascidian, Didemnum chartaceum (Sluiter, 1909). J. Org. Chem. 1988, 53, 4570-4574.
    • (1988) J. Org. Chem. , vol.53 , pp. 4570-4574
    • Lindquist, N.1    Fenical, W.2    Van Duyne, G.D.3
  • 99
    • 0037419451 scopus 로고    scopus 로고
    • Dictyodendrins A-E the first telomerase inhibitory marine natural products from the sponge, Dictyodendrilla verongiformis
    • Warabi, K.; Matsunaga, S.; van Soest, R.W.M.; Fusetani, N. Dictyodendrins A-E, the first telomerase inhibitory marine natural products from the sponge, Dictyodendrilla verongiformis. J. Org. Chem. 2003, 68, 2735-2770.
    • (2003) J. Org. Chem. , vol.68 , pp. 2735-2770
    • Warabi, K.1    Matsunaga, S.2    Van Soest, R.W.M.3    Fusetani, N.4
  • 101
    • 0028268353 scopus 로고
    • Polycitone A and polycitrins A and B: New alkaloids from the marine ascidian, Polycitor sp
    • Rudi, A.; Goldberg, I.; Stein, Z.; Frolow, F.; Benayahu, Y.; Schleyer, M.; Kashman, Y. Polycitone A and polycitrins A and B: New alkaloids from the marine ascidian, Polycitor sp. J. Org. Chem. 1994, 59, 999-1003.
    • (1994) J. Org. Chem. , vol.59 , pp. 999-1003
    • Rudi, A.1    Goldberg, I.2    Stein, Z.3    Frolow, F.4    Benayahu, Y.5    Schleyer, M.6    Kashman, Y.7
  • 102
    • 0033571010 scopus 로고    scopus 로고
    • Polycitone A a novel and potent general inhibitor of retroviral reverse transcriptases and cellular DNA polymerases
    • Loya, S.; Rudi, A.; Kashman, Y.; Hizi, A. Polycitone A, a novel and potent general inhibitor of retroviral reverse transcriptases and cellular DNA polymerases. Biochem. J. 1999, 344, 85-92.
    • (1999) Biochem. J. , vol.344 , pp. 85-92
    • Loya, S.1    Rudi, A.2    Kashman, Y.3    Hizi, A.4
  • 103
    • 0033935999 scopus 로고    scopus 로고
    • Polycitone B and prepolycitrin A: Two novel alkaloids from the marine ascidian, Polycitor africanus
    • Rudi, A.; Evan, T.; Akin, M.; Kashman, Y. Polycitone B and prepolycitrin A: Two novel alkaloids from the marine ascidian, Polycitor africanus. J. Nat. Prod. 2000, 63, 832-833.
    • (2000) J. Nat. Prod. , vol.63 , pp. 832-833
    • Rudi, A.1    Evan, T.2    Akin, M.3    Kashman, Y.4
  • 104
    • 0343612084 scopus 로고
    • A complex pyrrolo-oxazinone and its derivate isolated from tunicates
    • Yoshida, W.; Lee, K.; Carroll, A.; Scheuer, P. A complex pyrrolo-oxazinone and its derivate isolated from tunicates. Helv. Chim. Acta 1992, 75, 1721-1725.
    • (1992) Helv. Chim. Acta , vol.75 , pp. 1721-1725
    • Yoshida, W.1    Lee, K.2    Carroll, A.3    Scheuer, P.4
  • 105
    • 0033579656 scopus 로고    scopus 로고
    • The application of vinylogous iminium salt derivatives to a regiocontrolled and efficient relay synthesis of lukianol A and related marine natural products
    • Gupton, J.; Krumpe, K.; Burnham, B.; Webb, T.; Shuford, J.; Siberoski, J. The application of vinylogous iminium salt derivatives to a regiocontrolled and efficient relay synthesis of lukianol A and related marine natural products. Tetrahedron 1999, 55, 14515-14522.
    • (1999) Tetrahedron , vol.55 , pp. 14515-14522
    • Gupton, J.1    Krumpe, K.2    Burnham, B.3    Webb, T.4    Shuford, J.5    Siberoski, J.6
  • 106
    • 33845530046 scopus 로고    scopus 로고
    • Pyrrole natural products with antitumor properties
    • Gupton, J.T. Pyrrole natural products with antitumor properties. Top. Heterocycl. Chem. 2006, 2, 53-92.
    • (2006) Top. Heterocycl. Chem. , vol.2 , pp. 53-92
    • Gupton, J.T.1
  • 107
    • 77951243863 scopus 로고    scopus 로고
    • Characterization of a novel type of oxidative decarboxylase involved in the biosynthesis of the styryl moiety of chondrochloren from an acylated tyrosine
    • Rachid, S.; Revemann, O.; Dauth, C.; Kazmaier, U.; Muller, R. Characterization of a novel type of oxidative decarboxylase involved in the biosynthesis of the styryl moiety of chondrochloren from an acylated tyrosine. J. Biol. Chem. 2010, 285, 12482-12489.
    • (2010) J. Biol. Chem. , vol.285 , pp. 12482-12489
    • Rachid, S.1    Revemann, O.2    Dauth, C.3    Kazmaier, U.4    Muller, R.5
  • 108
    • 0035999729 scopus 로고    scopus 로고
    • Comparative biochemistry of eumelanogenesis and the protective roles of phenoloxidase and melanin in insects
    • Sugumaran, M. Comparative biochemistry of eumelanogenesis and the protective roles of phenoloxidase and melanin in insects. Pigment Cell Res. 2002, 15, 2-9.
    • (2002) Pigment Cell Res. , vol.15 , pp. 2-9
    • Sugumaran, M.1
  • 109
    • 0024806426 scopus 로고
    • Unusual intramolecular cyclization and side chain desaturation of carboxyethyl-o-benzoquinone derivatives
    • Sugumaran, M.; Dali, H.; Kundzicz, H.; Semensi, V. Unusual intramolecular cyclization and side chain desaturation of carboxyethyl-o-benzoquinone derivatives. Bioorg. Chem. 1989, 17, 443-453.
    • (1989) Bioorg. Chem. , vol.17 , pp. 443-453
    • Sugumaran, M.1    Dali, H.2    Kundzicz, H.3    Semensi, V.4
  • 110
    • 0024978514 scopus 로고
    • Nonenzymatic transformations of enzymatically generated N-acetyl dopamine quinone and isomeric dihydrocaffeiyl methylamide quinone
    • Sugumaran, M.; Semensi, V.; Dali, H.; Saul, S.J. Nonenzymatic transformations of enzymatically generated N-acetyl dopamine quinone and isomeric dihydrocaffeiyl methylamide quinone. FEBS Lett. 1989, 255, 345-349.
    • (1989) FEBS Lett. , vol.255 , pp. 345-349
    • Sugumaran, M.1    Semensi, V.2    Dali, H.3    Saul, S.J.4
  • 111
    • 0026029533 scopus 로고
    • Ab-dehydro-3,4-dihydroxyphenylalanine derivatives: Rate and mechanism of formation
    • Rzepecki, L.M.; Waite, J.H. a,b-dehydro-3,4-dihydroxyphenylalanine derivatives: Rate and mechanism of formation. Arch. Biochem. Biophys. 1991, 285, 27-36.
    • (1991) Arch. Biochem. Biophys. , vol.285 , pp. 27-36
    • Rzepecki, L.M.1    Waite, J.H.2
  • 112
    • 0029206656 scopus 로고
    • Model sclerotization studies. 3. Cuticular enzyme catalyzed oxidation of peptidyl model tyrosine and dopa derivatives
    • Sugumaran, M.; Ricketts, D. Model sclerotization studies. 3. Cuticular enzyme catalyzed oxidation of peptidyl model tyrosine and dopa derivatives. Arch. Insect Biochem. Physiol. 1995, 28, 17-32.
    • (1995) Arch. Insect Biochem. Physiol. , vol.28 , pp. 17-32
    • Sugumaran, M.1    Ricketts, D.2
  • 113
    • 0024285098 scopus 로고
    • A novel quinone: Quinone methide isomerase generates quinone methides in insect cuticle
    • Saul, S.J.; Sugumaran, M. A novel quinone: Quinone methide isomerase generates quinone methides in insect cuticle. FEBS Lett. 1988, 237, 155-158.
    • (1988) FEBS Lett. , vol.237 , pp. 155-158
    • Saul, S.J.1    Sugumaran, M.2
  • 114
    • 0025036539 scopus 로고
    • 4-Alkyl-o-quinone/2-hydroxy-p-quinone methide isomerase from the larval hemolymph of Sarcophaga bullata. I. Purification and characterization of enzyme-catalyzed reaction
    • Saul, S.J.; Sugumaran, M. 4-Alkyl-o-quinone/2-hydroxy-p-quinone methide isomerase from the larval hemolymph of Sarcophaga bullata. I. Purification and characterization of enzyme-catalyzed reaction. J. Biol. Chem. 1990, 265, 16992-16999.
    • (1990) J. Biol. Chem. , vol.265 , pp. 16992-16999
    • Saul, S.J.1    Sugumaran, M.2
  • 115
    • 0024978566 scopus 로고
    • N-acetyldopamine quinone methide/12-dehydro-N-acetyldopamine tautomerase. A new enzyme involved in sclerotization of insect cuticle
    • Saul, S.J.; Sugumaran, M. N-acetyldopamine quinone methide/1,2-dehydro-N- acetyldopamine tautomerase. A new enzyme involved in sclerotization of insect cuticle. FEBS Lett. 1989, 255, 340-344.
    • (1989) FEBS Lett. , vol.255 , pp. 340-344
    • Saul, S.J.1    Sugumaran, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.