메뉴 건너뛰기




Volumn 26, Issue 3, 2015, Pages 313-316

Prenylated indole alkaloids from the marine-derived fungus Paecilomyces variotii

Author keywords

Cytotoxicity; Indolediketopiperazine; Marine algal derived fungus; Natural products; Paecilomyces variotii

Indexed keywords


EID: 84939935454     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2014.11.020     Document Type: Article
Times cited : (42)

References (19)
  • 1
    • 79961087501 scopus 로고    scopus 로고
    • Biosynthetic studies of the notoamides: Isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide
    • J.M. Finefield, H. Kato, and T.J. Greshock Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide Org. Lett. 13 2011 3802 3805
    • (2011) Org. Lett. , vol.13 , pp. 3802-3805
    • Finefield, J.M.1    Kato, H.2    Greshock, T.J.3
  • 2
    • 84860326643 scopus 로고    scopus 로고
    • Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids
    • J.M. Finefield, J.C. Frisvad, D.H. Sherman, and R.M. Williams Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids J. Nat. Prod. 75 2012 812 833
    • (2012) J. Nat. Prod. , vol.75 , pp. 812-833
    • Finefield, J.M.1    Frisvad, J.C.2    Sherman, D.H.3    Williams, R.M.4
  • 3
    • 84863625035 scopus 로고    scopus 로고
    • Secondary metabolites from a marine-derived fungus Aspergillus carneus Blochwitz
    • O.I. Zhuravleva, S.S. Afiyatullov, and V.A. Denisenko Secondary metabolites from a marine-derived fungus Aspergillus carneus Blochwitz Phytochemistry 80 2012 123 131
    • (2012) Phytochemistry , vol.80 , pp. 123-131
    • Zhuravleva, O.I.1    Afiyatullov, S.S.2    Denisenko, V.A.3
  • 4
    • 84877109615 scopus 로고    scopus 로고
    • Isolation and photoinduced conversion of 6-epi-stephacidins from Aspergillus taichungensis
    • S.X. Cai, Y.P. Luan, and X.L. Kong Isolation and photoinduced conversion of 6-epi-stephacidins from Aspergillus taichungensis Org. Lett. 15 2013 2168 2171
    • (2013) Org. Lett. , vol.15 , pp. 2168-2171
    • Cai, S.X.1    Luan, Y.P.2    Kong, X.L.3
  • 6
    • 77956422779 scopus 로고    scopus 로고
    • Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp
    • Y. Ding, J.R. de Wet, and J. Cavalcoli Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp. J. Am. Chem. Soc. 132 2010 12733 12740
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12733-12740
    • Ding, Y.1    De Wet, J.R.2    Cavalcoli, J.3
  • 8
    • 34447628311 scopus 로고    scopus 로고
    • A new naphthoquinoneimine derivative from the marine algal-derived endophytic fungus Aspergillus niger EN-13
    • Y. Zhang, X.M. Li, C.Y. Wang, and B.G. Wang A new naphthoquinoneimine derivative from the marine algal-derived endophytic fungus Aspergillus niger EN-13 Chin. Chem. Lett. 18 2007 951 953
    • (2007) Chin. Chem. Lett. , vol.18 , pp. 951-953
    • Zhang, Y.1    Li, X.M.2    Wang, C.Y.3    Wang, B.G.4
  • 9
    • 84883826424 scopus 로고    scopus 로고
    • Cytotoxic anthranilic acid derivatives from deep sea sediment-derived fungus Penicillium paneum SD-44
    • C.S. Li, X.M. Li, S.S. Gao, Y.H. Lu, and B.G. Wang Cytotoxic anthranilic acid derivatives from deep sea sediment-derived fungus Penicillium paneum SD-44 Mar. Drugs 11 2013 3068 3076
    • (2013) Mar. Drugs , vol.11 , pp. 3068-3076
    • Li, C.S.1    Li, X.M.2    Gao, S.S.3    Lu, Y.H.4    Wang, B.G.5
  • 10
    • 84890283719 scopus 로고    scopus 로고
    • Antioxidant metabolites from marine alga-derived fungus Aspergillus wentii EN-48
    • X. Li, X.M. Li, G.M. Xu, C.S. Li, and B.G. Wang Antioxidant metabolites from marine alga-derived fungus Aspergillus wentii EN-48 Phytochem. Lett. 7 2014 120 123
    • (2014) Phytochem. Lett. , vol.7 , pp. 120-123
    • Li, X.1    Li, X.M.2    Xu, G.M.3    Li, C.S.4    Wang, B.G.5
  • 11
    • 84879492629 scopus 로고    scopus 로고
    • Secondary metabolites from Penicillium pinophilum SD-272, a marine sediment-derived fungus
    • M.H. Wang, X.M. Li, C.S. Li, N.Y. Ji, and B.G. Wang Secondary metabolites from Penicillium pinophilum SD-272, a marine sediment-derived fungus Mar. Drugs 11 2013 2230 2238
    • (2013) Mar. Drugs , vol.11 , pp. 2230-2238
    • Wang, M.H.1    Li, X.M.2    Li, C.S.3    Ji, N.Y.4    Wang, B.G.5
  • 12
    • 84910062017 scopus 로고    scopus 로고
    • Varioxepine A, a 3H-oxepine-containing alkaloid with a new oxa-cage from the marine algal-derived endophytic fungus Paecilomyces variotii
    • P. Zhang, A. Mándi, and X.M. Li Varioxepine A, a 3H-oxepine-containing alkaloid with a new oxa-cage from the marine algal-derived endophytic fungus Paecilomyces variotii Org. Lett. 16 2014 4834 4837
    • (2014) Org. Lett. , vol.16 , pp. 4834-4837
    • Zhang, P.1    Mándi, A.2    Li, X.M.3
  • 13
    • 33845923678 scopus 로고    scopus 로고
    • Chaetopyranin, a benzaldehyde derivative, and other related metabolites from Chaetomium globosum, an endophytic fungus derived from the marine red alga Polysiphonia urceolata
    • S. Wang, X.M. Li, and F. Teuscher Chaetopyranin, a benzaldehyde derivative, and other related metabolites from Chaetomium globosum, an endophytic fungus derived from the marine red alga Polysiphonia urceolata J. Nat. Prod. 69 2006 1622 1625
    • (2006) J. Nat. Prod. , vol.69 , pp. 1622-1625
    • Wang, S.1    Li, X.M.2    Teuscher, F.3
  • 14
    • 84888438231 scopus 로고    scopus 로고
    • A cytotoxic pyrrolidinoindoline diketopiperazine dimer from the algal fungus Eurotium herbariorum HT-2
    • Y. Li, K.L. Sun, and Y. Wang A cytotoxic pyrrolidinoindoline diketopiperazine dimer from the algal fungus Eurotium herbariorum HT-2 Chin. Chem. Lett. 24 2013 1049 1052
    • (2013) Chin. Chem. Lett. , vol.24 , pp. 1049-1052
    • Li, Y.1    Sun, K.L.2    Wang, Y.3
  • 15
    • 33744460793 scopus 로고    scopus 로고
    • Aurilides B and C, cancer cell toxins from a Papua New Guinea collection of the marine cyanobacterium Lyngbya majuscula
    • B.H. Han, H. Gross, D.E. Goeger, S.L. Mooberry, and W.G. Gerwick Aurilides B and C, cancer cell toxins from a Papua New Guinea collection of the marine cyanobacterium Lyngbya majuscula J. Nat. Prod. 69 2006 572 575
    • (2006) J. Nat. Prod. , vol.69 , pp. 572-575
    • Han, B.H.1    Gross, H.2    Goeger, D.E.3    Mooberry, S.L.4    Gerwick, W.G.5
  • 16
    • 34249104049 scopus 로고    scopus 로고
    • Notoamides A-D: Prenylated indole alkaloids isolated from a marine-derived fungus, Aspergillus sp
    • H. Kato, T. Yoshida, and T. Tokue Notoamides A-D: prenylated indole alkaloids isolated from a marine-derived fungus, Aspergillus sp. Angew. Chem. Int. Ed. 46 2007 2254 2256
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 2254-2256
    • Kato, H.1    Yoshida, T.2    Tokue, T.3
  • 17
    • 0029856862 scopus 로고    scopus 로고
    • Sclerotiamide: A new member of the paraherquamide class with potent antiinsectan activity from the sclerotia of Aspergillus sclerotiorum
    • A.C. Whyte, J.B. Gloer, D.T. Wicklow, and P.F. Dowd Sclerotiamide: a new member of the paraherquamide class with potent antiinsectan activity from the sclerotia of Aspergillus sclerotiorum J. Nat. Prod. 59 1996 1093 1095
    • (1996) J. Nat. Prod. , vol.59 , pp. 1093-1095
    • Whyte, A.C.1    Gloer, J.B.2    Wicklow, D.T.3    Dowd, P.F.4
  • 18
    • 44049099382 scopus 로고    scopus 로고
    • Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600
    • T.J. Greshock, A.W. Grubbs, and P. Jiao Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600 Angew. Chem. Int. Ed. 47 2008 3573 3577
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3573-3577
    • Greshock, T.J.1    Grubbs, A.W.2    Jiao, P.3
  • 19
    • 33845184957 scopus 로고
    • Remarkable, enantio-divergent biogenesis of brevianamide A and B
    • R.M. Williams, E. Kwast, H. Coffman, and T. Glinka Remarkable, enantio-divergent biogenesis of brevianamide A and B J. Am. Chem. Soc. 111 1989 3064 3065
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 3064-3065
    • Williams, R.M.1    Kwast, E.2    Coffman, H.3    Glinka, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.