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Volumn 46, Issue 20, 2003, Pages 4342-4350

Structures and cytotoxic properties of trichoverroids and their macrolide analogues produced by saltwater culture of Myrothecium verrucaria

Author keywords

[No Author keywords available]

Indexed keywords

13' ACETYLTRICHOVERRIN B; 3 HYDROXYRORIDIN E; EPIRORIDIN E; ISORORIDINE A; MACROLIDE; MIOPHYTOCEN C; RORIDIN A; RORIDIN L; RORIDIN M; TRICHOTHECENE DERIVATIVE; TRICHOVERRIN A; TRICHOVERRIN B; TRICHOVERROID DERIVATIVE; UNCLASSIFIED DRUG; VERRUCARIN A; VERRUCARIN M;

EID: 0141792688     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm030090t     Document Type: Article
Times cited : (78)

References (58)
  • 1
    • 0027365170 scopus 로고
    • Trichoharzin, a new polyketide produced by the imperfect fungus Trichoderma harzianum separated from the marine sponge Micale cecilia
    • Kobayashi, M.; Uehara, H.; Matsunami, K.; Aoki, S.; Kitagawa, I. Trichoharzin, a New Polyketide Produced by the Imperfect Fungus Trichoderma harzianum Separated from the Marine Sponge Micale cecilia. Tetrahedron Lett. 1993, 34, 7925-7928.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 7925-7928
    • Kobayashi, M.1    Uehara, H.2    Matsunami, K.3    Aoki, S.4    Kitagawa, I.5
  • 2
    • 0028117973 scopus 로고
    • Chloriolines A-C, chlorinated sesquiterpenes produced by fungal cultures separated from a Jaspis marine sponge
    • Cheng, X. C.; Varoglu, M.; Abrell, L. M.; Crews P.; Lobkovsky E.; Clardy J. Chloriolines A-C, Chlorinated Sesquiterpenes Produced by Fungal Cultures Separated from a Jaspis Marine Sponge. J. Org. Chem. 1994, 59, 6344-6348.
    • (1994) J. Org. Chem. , vol.59 , pp. 6344-6348
    • Cheng, X.C.1    Varoglu, M.2    Abrell, L.M.3    Crews, P.4    Lobkovsky, E.5    Clardy, J.6
  • 3
    • 0030577497 scopus 로고    scopus 로고
    • A new polyketide secocurvularin, from the salt water culture of a sponge derived fungus
    • Abrell, L. M.; Borgeson, B.; Crews, P. A New Polyketide, Secocurvularin, from the Salt Water Culture of a Sponge Derived Fungus. Tetrahedron Lett. 1996, 37, 8983-8984.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8983-8984
    • Abrell, L.M.1    Borgeson, B.2    Crews, P.3
  • 4
    • 0000260530 scopus 로고    scopus 로고
    • Asperazine, a selective cytotoxic alkaloid from a sponge-derived culture of Aspergillus niger
    • Isolation: Varoglu, M.; Corbett, T. H.; Valariote, F. A.; Crews, P. Asperazine, a Selective Cytotoxic Alkaloid from a Sponge-Derived Culture of Aspergillus niger. J. Org. Chem. 1997, 62, 7078-7079.
    • (1997) J. Org. Chem. , vol.62 , pp. 7078-7079
    • Varoglu, M.1    Corbett, T.H.2    Valariote, F.A.3    Crews, P.4
  • 5
    • 0035955155 scopus 로고    scopus 로고
    • Total synthesis of asperazine
    • (b) Synthesis: Govek, S. P.; Overman, L. E. Total Synthesis of Asperazine. J. Am. Chem. Soc. 2001, 123, 9468-9469.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9468-9469
    • Govek, S.P.1    Overman, L.E.2
  • 6
    • 0032567410 scopus 로고    scopus 로고
    • Vertinoid polyketides from the saltwater culture of the fungus Trichoderma longibrachiatum separated from a Haliclona marine sponge
    • Isolation: Sperry, S.; Samuels, G. J.; Crews, P. Vertinoid Polyketides from the Saltwater Culture of the Fungus Trichoderma longibrachiatum Separated from a Haliclona Marine Sponge. J. Org. Chem. 1998, 63, 10011-10014.
    • (1998) J. Org. Chem. , vol.63 , pp. 10011-10014
    • Sperry, S.1    Samuels, G.J.2    Crews, P.3
  • 8
    • 33750276979 scopus 로고    scopus 로고
    • Absolute stereostructures of novel cytotoxic metabolites, gymnastatins A-E, from a Gymnascella species separated from a Halichondria sponge
    • Isolation: Amagata, T.; Doi, M.; Ohta, T.; Minoura, K.; Numata, A. Absolute Stereostructures of Novel Cytotoxic Metabolites, Gymnastatins A-E, from a Gymnascella Species Separated from a Halichondria Sponge. J. Chem. Soc., Perkin Trans. 1 1998, 21, 3585-3599.
    • (1998) J. Chem. Soc., Perkin Trans. 1 , vol.21 , pp. 3585-3599
    • Amagata, T.1    Doi, M.2    Ohta, T.3    Minoura, K.4    Numata, A.5
  • 9
    • 0033950538 scopus 로고    scopus 로고
    • Total synthesis of a novel metabolite gymnastatin A
    • (b) Synthesis: Gurjar, M. K.; Bhaket, P. Total Synthesis of a Novel Metabolite Gymnastatin A. Heterocycles 2000, 53, 143-149.
    • (2000) Heterocycles , vol.53 , pp. 143-149
    • Gurjar, M.K.1    Bhaket, P.2
  • 10
    • 0141669387 scopus 로고    scopus 로고
    • HPLC-UV -MS, -NMR and -CD as useful tools in the search for new metabolites from sponge derived fungi
    • 3rd European Conference on Marine Natural Products, Elmau Castle, Bavaria, Sept 15-20, 2002; Munich, Abstract
    • Lang, G.; Steffens, S.; Schaumann, K.; Bringmann, G. HPLC-UV, -MS, -NMR and -CD as Useful Tools in the Search for New Metabolites from Sponge Derived Fungi. Scientific Programme, Book of Abstracts, List of Participants; 3rd European Conference on Marine Natural Products, Elmau Castle, Bavaria, Sept 15-20, 2002; Munich, 2002, Abstract p 67.
    • (2002) Scientific Programme, Book of Abstracts, List of Participants , pp. 67
    • Lang, G.1    Steffens, S.2    Schaumann, K.3    Bringmann, G.4
  • 11
    • 0141781326 scopus 로고    scopus 로고
    • Biogenetically diverse secondary metabolites from sponge-associated fungi
    • 3rd European Conference on Marine Natural Proudcts, Elmau Castle, Bavaria, September 15-20, 2002; Munich, Abstract
    • Ebel, R.; Lin, W. H.; Edrada, R. A.; Proksch, P. Biogenetically Diverse Secondary Metabolites from Sponge-Associated Fungi. Scientific Programme, Book of Abstracts, List of Participants; 3rd European Conference on Marine Natural Proudcts, Elmau Castle, Bavaria, September 15-20, 2002; Munich, 2002, Abstract, p 67.
    • (2002) Scientific Programme, Book of Abstracts, List of Participants , pp. 67
    • Ebel, R.1    Lin, W.H.2    Edrada, R.A.3    Proksch, P.4
  • 15
    • 0035142057 scopus 로고    scopus 로고
    • Laboratory culture of the myxomycetes: Formation of fruiting bodies of didymium bahiense and its plasmodial production of makaluvamine A
    • Ishibashi, M.; Iwasaki, T.; Imai, S.; Sakamoto, S.; Yamaguchi, K.; Ito, A. Laboratory Culture of the Myxomycetes: Formation of Fruiting Bodies of Didymium bahiense and Its Plasmodial Production of Makaluvamine A. J. Nat. Prod. 2001, 64, 108-110.
    • (2001) J. Nat. Prod. , vol.64 , pp. 108-110
    • Ishibashi, M.1    Iwasaki, T.2    Imai, S.3    Sakamoto, S.4    Yamaguchi, K.5    Ito, A.6
  • 16
    • 0031881662 scopus 로고    scopus 로고
    • Isolation and cytotoxic evaluation of marine sponge-derived norterpene peroxides
    • Sperry, S.; Valeriote, F. A.; Corbett, T. H.; Crews, P. Isolation and Cytotoxic Evaluation of Marine Sponge-Derived Norterpene Peroxides. J. Nat. Prod. 1998, 61, 241-247.
    • (1998) J. Nat. Prod. , vol.61 , pp. 241-247
    • Sperry, S.1    Valeriote, F.A.2    Corbett, T.H.3    Crews, P.4
  • 21
    • 0032864079 scopus 로고    scopus 로고
    • Stereochemistry of the roridins. Diasteromers of roridin E
    • Jarvis, B. B.; Wang, S. Stereochemistry of the Roridins. Diasteromers of Roridin E. J. Nat. Prod. 1999, 62, 1284-1289.
    • (1999) J. Nat. Prod. , vol.62 , pp. 1284-1289
    • Jarvis, B.B.1    Wang, S.2
  • 23
    • 0343339950 scopus 로고    scopus 로고
    • Effects of four trichothecen mycotoxins on activation marker expression and cell proliferation of human lymphocytes in culture
    • Johannisson, A.; Björkhag, B.; Hansson, W.; Gadhasson, I.-L.; Thuvander, A. Effects of Four Trichothecen Mycotoxins on Activation Marker Expression and Cell Proliferation of Human Lymphocytes in Culture. Cell Biol. Toxicol. 1999, 15, 203-215.
    • (1999) Cell Biol. Toxicol. , vol.15 , pp. 203-215
    • Johannisson, A.1    Björkhag, B.2    Hansson, W.3    Gadhasson, I.-L.4    Thuvander, A.5
  • 24
    • 0033952517 scopus 로고    scopus 로고
    • Lipopolysaccharide and the trichothecene vomitoxin (deoxynivalenol) synergistically induce apoptosis in murine lymphoid organs
    • Zhou, H. R.; Harkema, J. R.; Hotchkiss, J. A.; Yan, D.; Roth, R. A.; Pestka, J. J. Lipopolysaccharide and the Trichothecene Vomitoxin (Deoxynivalenol) Synergistically Induce Apoptosis in Murine Lymphoid Organs. Toxicol. Sci. 2000, 53, 253-263.
    • (2000) Toxicol. Sci. , vol.53 , pp. 253-263
    • Zhou, H.R.1    Harkema, J.R.2    Hotchkiss, J.A.3    Yan, D.4    Roth, R.A.5    Pestka, J.J.6
  • 25
    • 0033026397 scopus 로고    scopus 로고
    • Antimalarial activity of macrocyclic trichothecenes isolated from the fungus Myrothecium verrucaria
    • Isaka, M.; Punya, J.; Lertwerawat, Y.; Tanticharoen, M.; Thebtaranonth, Y. Antimalarial Activity of Macrocyclic Trichothecenes Isolated from the Fungus Myrothecium verrucaria. J. Nat. Prod. 1999, 62, 329-331.
    • (1999) J. Nat. Prod. , vol.62 , pp. 329-331
    • Isaka, M.1    Punya, J.2    Lertwerawat, Y.3    Tanticharoen, M.4    Thebtaranonth, Y.5
  • 26
    • 0036216228 scopus 로고    scopus 로고
    • Evaluation of the antiviral activity against Junin virus of macrocyclic trichothecenes produced by the hypocrealean epibiont of Baccharis cordifolia
    • Garcia, C. C.; Rosso, M. L.; Bertoni, M. D.; Maier, M. S.; Damonte, E. B. Evaluation of the Antiviral Activity Against Junin Virus of Macrocyclic Trichothecenes Produced by the Hypocrealean Epibiont of Baccharis cordifolia. Planta Med. 2002, 68, 209-212.
    • (2002) Planta Med. , vol.68 , pp. 209-212
    • Garcia, C.C.1    Rosso, M.L.2    Bertoni, M.D.3    Maier, M.S.4    Damonte, E.B.5
  • 27
    • 0017389695 scopus 로고
    • Verrucarins roridins. 34th communication. Verrucarin K, the first natural trichothecene derivative lacking the 12, 13-epoxy group
    • Breitenstein, W.; Tamm, C. Verrucarins Roridins. 34th Communication. Verrucarin K, the First Natural Trichothecene Derivative Lacking the 12, 13-Epoxy Group. Helv. Chim. Acta 1977, 60, 1522-1527.
    • (1977) Helv. Chim. Acta , vol.60 , pp. 1522-1527
    • Breitenstein, W.1    Tamm, C.2
  • 28
    • 0008953251 scopus 로고
    • New trichoverroids from myrothecium verrucaria: Verrol and 12,13-deoxytrichodermadiene
    • (b) Jarvis, B. B.; Vrudhula, V. M.; Midiwo, J. O.; Mazzola, E. P. New Trichoverroids from Myrothecium verrucaria: Verrol and 12,13-Deoxytrichodermadiene. J. Org. Chem. 1983, 48, 2576-2578.
    • (1983) J. Org. Chem. , vol.48 , pp. 2576-2578
    • Jarvis, B.B.1    Vrudhula, V.M.2    Midiwo, J.O.3    Mazzola, E.P.4
  • 29
    • 0024661550 scopus 로고
    • 12, 13-deoxytrichoverrins from Myrothecium verrucaria
    • (c) Jarvis, B. B.; Midiwo, J. O.; Guo, M.-D. 12, 13-Deoxytrichoverrins from Myrothecium verrucaria. J. Nat. Prod, 1989, 52, 663-665.
    • (1989) J. Nat. Prod. , vol.52 , pp. 663-665
    • Jarvis, B.B.1    Midiwo, J.O.2    Guo, M.-D.3
  • 30
    • 0022244804 scopus 로고
    • Macrocyclic trichothecenes: Cause of livestock poisoning by the Brazilian plant Baccharis coridifolia
    • (d) Habermehl, G. G.; Busam, L.; Heydel, P.; Mebs, D.; Tokarnia, C. H.; Doebereiner, J.; Spraul, M. Macrocyclic Trichothecenes: Cause of Livestock Poisoning by the Brazilian Plant Baccharis coridifolia. Toxicon 1985, 23, 731-745.
    • (1985) Toxicon , vol.23 , pp. 731-745
    • Habermehl, G.G.1    Busam, L.2    Heydel, P.3    Mebs, D.4    Tokarnia, C.H.5    Doebereiner, J.6    Spraul, M.7
  • 31
    • 0035089039 scopus 로고    scopus 로고
    • A new macrocytotoxic trichothecene 12, 13-deoxyroridin E, produced by the marine-derived fungus Myrothecium verrucaria
    • (e) Namikoshi, M.; Akano, K.; Meguro, S.; Kasuga, I.; Mine, Y.; Takahashi, T.; Kobayashi, H. A New Macrocytotoxic Trichothecene, 12, 13-Deoxyroridin E, Produced by the Marine-Derived Fungus Myrothecium verrucaria. J. Nat. Prod. 2001, 64, 396-398.
    • (2001) J. Nat. Prod. , vol.64 , pp. 396-398
    • Namikoshi, M.1    Akano, K.2    Meguro, S.3    Kasuga, I.4    Mine, Y.5    Takahashi, T.6    Kobayashi, H.7
  • 32
    • 0021339117 scopus 로고
    • Antileukemic compounds derived by chemical modification of macrocyclic trichothecenes. 2. Derivatives of roridin A and H and verrucarin A and J
    • Jarvis, B. B.; Midiwo, J. O.; Mazzola, E. P. Antileukemic Compounds Derived by Chemical Modification of Macrocyclic Trichothecenes. 2. Derivatives of Roridin A and H and Verrucarin A and J. J. Med. Chem. 1984, 27, 239-244.
    • (1984) J. Med. Chem. , vol.27 , pp. 239-244
    • Jarvis, B.B.1    Midiwo, J.O.2    Mazzola, E.P.3
  • 34
    • 0021062301 scopus 로고
    • Total synthesis of the trichothecene mycotoxin anguidine
    • (b) Brooks, D. W.; Grothaus, P. G.; Mazdiyasni, H. Total Synthesis of the Trichothecene Mycotoxin Anguidine. J. Am. Chem. Soc. 1983,105, 4472-4473.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 4472-4473
    • Brooks, D.W.1    Grothaus, P.G.2    Mazdiyasni, H.3
  • 36
    • 0031910079 scopus 로고    scopus 로고
    • Characterization of the gene cluster for biosynthesis of macrocyclic trichothecenes in Myrothecium roridum
    • Trapp, S. C.; Hohn, T. M.; McCormic, S.; Jarvis, B. B. Characterization of the Gene Cluster for Biosynthesis of Macrocyclic Trichothecenes in Myrothecium roridum. Mol. Gen. Genet. 1998, 257, 421-432.
    • (1998) Mol. Gen. Genet. , vol.257 , pp. 421-432
    • Trapp, S.C.1    Hohn, T.M.2    McCormic, S.3    Jarvis, B.B.4
  • 37
    • 0035206971 scopus 로고    scopus 로고
    • New macrocyclic trichothecene group antitumor antibiotics, from Myrothecium verrucaria
    • Murakami, Y.; Okuda, T.; Shindo, K. Roridin L, M and Verrucarin M, New Macrocyclic Trichothecene Group Antitumor Antibiotics, from Myrothecium verrucaria. J. Antibiot. 2001, 54, 980-983.
    • (2001) J. Antibiot. , vol.54 , pp. 980-983
    • Murakami, Y.1    Okuda, T.2    Shindo, K.3    Roridin, L.M.4    Verrucarin, M.5
  • 38
    • 0016591292 scopus 로고
    • 13C NMR-spectroscopy of the trichothecane derivatives verrucarol, verrucarins A and B and roridins A, D and H
    • 13C NMR-Spectroscopy of the Trichothecane Derivatives Verrucarol, Verrucarins A and B and Roridins A, D and H. Helv. Chim. Acta 1975, 58, 1172-1180.
    • (1975) Helv. Chim. Acta , vol.58 , pp. 1172-1180
    • Breitenstein, W.1    Tamm, C.2
  • 39
    • 0020385771 scopus 로고
    • Stereochemistry of roridins
    • Jarvis, B. B.; Midiwo, J. O. Stereochemistry of Roridins, J. Nat. Prod. 1982, 45, 440-448.
    • (1982) J. Nat. Prod. , vol.45 , pp. 440-448
    • Jarvis, B.B.1    Midiwo, J.O.2
  • 41
    • 0002201621 scopus 로고    scopus 로고
    • Cytotoxins, mycotoxins and drugs from a new deuteriomycete, acremonium neo-caledoniae, from the Southwestern Lagoon of New Caledonia
    • Laurent, D.; Guella, G.; Roquebert, M.-F.; Farinole, F.; Mancini, I.; Pietra, F. Cytotoxins, Mycotoxins and Drugs from a New Deuteriomycete, Acremonium neo-caledoniae, from the Southwestern Lagoon of New Caledonia. Planta Med. 2000, 66, 63-66.
    • (2000) Planta Med. , vol.66 , pp. 63-66
    • Laurent, D.1    Guella, G.2    Roquebert, M.-F.3    Farinole, F.4    Mancini, I.5    Pietra, F.6
  • 42
    • 0036691319 scopus 로고    scopus 로고
    • Employing dereplication and gradient 1D NMR methods to rapidly characterize sponge-derived sesterterpenes
    • Stessman, C. C.; Ebel, R.; Corvino, A. J.; Crews, P. Employing Dereplication and Gradient 1D NMR Methods to Rapidly Characterize Sponge-Derived Sesterterpenes. J. Nat. Prod. 2002, 65, 1183-1186.
    • (2002) J. Nat. Prod. , vol.65 , pp. 1183-1186
    • Stessman, C.C.1    Ebel, R.2    Corvino, A.J.3    Crews, P.4
  • 43
    • 0030590990 scopus 로고    scopus 로고
    • Trichothecinol A B and C, potent anti-tumor promoting sesquiterpenoids from the fungus Trichothecium roseum
    • Iida, A.; Konishi, K.; Kubo, H.; Tomioka, K.; Tokuda, H.; Nishino, H. Trichothecinol A, B and C, Potent Anti-tumor Promoting Sesquiterpenoids from the Fungus Trichothecium roseum. Tetrahedron Lett. 1996, 37, 9219-9220.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 9219-9220
    • Iida, A.1    Konishi, K.2    Kubo, H.3    Tomioka, K.4    Tokuda, H.5    Nishino, H.6
  • 44
    • 0034939644 scopus 로고    scopus 로고
    • Two new roridins isolated from Myrothecium sp
    • Wagenaar, M. M.; Clardy, J. Two New Roridins Isolated from Myrothecium sp. J. Antibiot. 2001, 54, 517-520.
    • (2001) J. Antibiot. , vol.54 , pp. 517-520
    • Wagenaar, M.M.1    Clardy, J.2
  • 46
    • 0017707533 scopus 로고
    • Evaluation of single agents and combinations of chemotherapeutic agents in mouse colon carcinomas
    • Corbett, T. H.; Griswold, D. P., Jr.; Roberts, B. J.; Peckham, J. C.; Schabel, F. M., Jr. Evaluation of single agents and combinations of chemotherapeutic agents in mouse colon carcinomas. Cancer 1977, 40, 2660-2680.
    • (1977) Cancer , vol.40 , pp. 2660-2680
    • Corbett, T.H.1    Griswold D.P., Jr.2    Roberts, B.J.3    Peckham, J.C.4    Schabel F.M., Jr.5
  • 47
  • 48
    • 0020611745 scopus 로고
    • Phase II evaluation of anguidine in central nervous system tumors; a Southwest Oncology Group Study
    • (b) Goodwin, J. W.; Bottomley, R. H.; Vaughn, C. B.; Frank, J.; Pugh, R. H. Phase II Evaluation of Anguidine in Central Nervous System Tumors; A Southwest Oncology Group Study. Cancer Treat. Rep. 1983, 67, 285-286.
    • (1983) Cancer Treat. Rep. , vol.67 , pp. 285-286
    • Goodwin, J.W.1    Bottomley, R.H.2    Vaughn, C.B.3    Frank, J.4    Pugh, R.H.5
  • 49
    • 0020046066 scopus 로고
    • Phase II study of anguidine in gastrointestinal malignancies: A Southwest Oncology Group Study
    • (c) Bukowski, R.; Vaughn, C.; Bottomley, R.; Chen, T. Phase II Study of Anguidine in Gastrointestinal Malignancies: A Southwest Oncology Group Study. Cancer Treat. Rep. 1982, 66, 381-383.
    • (1982) Cancer Treat. Rep. , vol.66 , pp. 381-383
    • Bukowski, R.1    Vaughn, C.2    Bottomley, R.3    Chen, T.4
  • 50
    • 0019426435 scopus 로고
    • Phase II trial of anguidine in patients with sarcomas unresponsive to prior chemotherapy: A Southwest Oncology Group Study
    • (d) Thigpen, J. T.; Vaughn, C.; Stuckey, W. J. Phase II Trial of Anguidine in Patients with Sarcomas Unresponsive to Prior Chemotherapy: A Southwest Oncology Group Study. Cancer Treat. Rep. 1981, 65, 881-882.
    • (1981) Cancer Treat. Rep. , vol.65 , pp. 881-882
    • Thigpen, J.T.1    Vaughn, C.2    Stuckey, W.J.3
  • 53
    • 0037138273 scopus 로고    scopus 로고
    • Phytotoxicity and mammalian cytotoxicity of macrocyclic trichothecene mycotoxins from Myrothecium verrucaria
    • Abbas, H. K.; Johnson, B. B.; Shier, W. T.; Tak, H.; Jarvis, B. B.; Boyette, C. D. Phytotoxicity and Mammalian Cytotoxicity of Macrocyclic Trichothecene Mycotoxins from Myrothecium verrucaria. Phytochemistry 2002, 59, 309-313.
    • (2002) Phytochemistry , vol.59 , pp. 309-313
    • Abbas, H.K.1    Johnson, B.B.2    Shier, W.T.3    Tak, H.4    Jarvis, B.B.5    Boyette, C.D.6
  • 55
    • 0028906786 scopus 로고
    • Some practical considerations and applications of the National-Cancer-Institute In-Vitro anticancer drug discovery screen
    • Boyd, M. R.; Pauli, K. D. Some Practical Considerations and Applications of the National-Cancer-Institute In-Vitro Anticancer Drug Discovery Screen. Drug Dev. Res, 1995, 34, 91-109.
    • (1995) Drug Dev. Res. , vol.34 , pp. 91-109
    • Boyd, M.R.1    Pauli, K.D.2
  • 56
    • 0033974253 scopus 로고    scopus 로고
    • Biosynthecally diverse compounds from a saltwater culture of sponge-derived Aspergillus niger
    • Varoglu, M.; Crews, P. Biosynthecally Diverse Compounds from a Saltwater Culture of Sponge-Derived Aspergillus niger. J. Nat. Prod. 2000, 63, 41-43.
    • (2000) J. Nat. Prod. , vol.63 , pp. 41-43
    • Varoglu, M.1    Crews, P.2
  • 57
    • 0000590748 scopus 로고
    • A revision of the supraspecific classification of the order dictyoceratida, dendroceratida, and verongida (class demospongia)
    • Bergquist, P. R. A Revision of the Supraspecific Classification of the Order Dictyoceratida, Dendroceratida, and Verongida (Class Demospongia). New Zeal. J. Zool. 1980, 7, 443-503.
    • (1980) New Zeal. J. Zool. , vol.7 , pp. 443-503
    • Bergquist, P.R.1
  • 58
    • 0000238570 scopus 로고
    • Dictyoceratida, dendroceratida and verongida from the new Caledonia Lagoon (Porifera: Demospongiae)
    • Bergquist, P. R. Dictyoceratida, Dendroceratida and Verongida from the New Caledonia Lagoon (Porifera: Demospongiae). Mem. Queens. Mus. 1995, 38, 1-51.
    • (1995) Mem. Queens. Mus. , vol.38 , pp. 1-51
    • Bergquist, P.R.1


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