메뉴 건너뛰기




Volumn 14, Issue , 2015, Pages 84-90

Aspernolides F and G, new butyrolactones from the endophytic fungus Aspergillus terreus

Author keywords

Anti leishmanial; Anti malarial; Anti microbial; Aspergillus terreus; Aspernolides; Butyrolactones; Meroterpenoids; Stigmasterol derivatives

Indexed keywords

AMPHOTERICIN B; ASPERNOLIDE F; ASPERNOLIDE G; BUTYROLACTONE; BUTYROLACTONE VI; CIPROFLOXACIN; STIGMAST 4 ENE 3 ONE; STIGMASTA 4,6,8(14), 22 TETRAEN 3 ONE; STIGMASTA 5,7,22 TRIEN 3 BETA OL; STIGMASTEROL; TERRETONIN; TERRETONIN A; UNCLASSIFIED DRUG;

EID: 84942765066     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2015.09.006     Document Type: Article
Times cited : (88)

References (38)
  • 1
    • 84896929629 scopus 로고    scopus 로고
    • New thiophene and flavonoid from Tagetes minuta leaves growing in Saudi Arabia
    • N.M. Al-Musayeib, G.A. Mohamed, S.R.M. Ibrahim, and S.A. Ross New thiophene and flavonoid from Tagetes minuta leaves growing in Saudi Arabia Molecules 19 2014 2819 2828
    • (2014) Molecules , vol.19 , pp. 2819-2828
    • Al-Musayeib, N.M.1    Mohamed, G.A.2    Ibrahim, S.R.M.3    Ross, S.A.4
  • 2
    • 84898869990 scopus 로고    scopus 로고
    • New phenyl derivatives from endophytic fungus Aspergillus flavipes AIL8 derived of mangrove plant Acanthus ilicifolius
    • Z. Bai, X. Lin, Y. Wang, J. Wang, X. Zhou, B. Yang, J. Liu, X. Yang, Y. Wang, and Y. Liu New phenyl derivatives from endophytic fungus Aspergillus flavipes AIL8 derived of mangrove plant Acanthus ilicifolius Fitoterapia 95 2014 194 202
    • (2014) Fitoterapia , vol.95 , pp. 194-202
    • Bai, Z.1    Lin, X.2    Wang, Y.3    Wang, J.4    Zhou, X.5    Yang, B.6    Liu, J.7    Yang, X.8    Wang, Y.9    Liu, Y.10
  • 3
    • 33746344302 scopus 로고    scopus 로고
    • Secondary metabolites from Euphorbia helioscopia and their vasodepressor activity
    • A. Barla, B.H. Hüsniye, S. Kültür, and S. Öksüz Secondary metabolites from Euphorbia helioscopia and their vasodepressor activity Turk. J. Chem. 30 2006 325 332
    • (2006) Turk. J. Chem. , vol.30 , pp. 325-332
    • Barla, A.1    Hüsniye, B.H.2    Kültür, S.3    Öksüz, S.4
  • 4
    • 0025685414 scopus 로고
    • Rapid chemosensitivity assay with human normal and tumor cells in vitro
    • E. Borenfreund, H. Babich, and N. Martin-Alguacil Rapid chemosensitivity assay with human normal and tumor cells in vitro In Vitro Cell Dev. Biol. 26 1990 1030 1034
    • (1990) In Vitro Cell Dev. Biol. , vol.26 , pp. 1030-1034
    • Borenfreund, E.1    Babich, H.2    Martin-Alguacil, N.3
  • 5
    • 27944454683 scopus 로고    scopus 로고
    • Antimicrobial butyrolactone i derivatives from the Ecuadorian soil fungus Aspergillus terreus Thorn. Var terreus
    • M.E. Cazar, G. Schmeda-Hirschmann, and L. Astudillo Antimicrobial butyrolactone I derivatives from the Ecuadorian soil fungus Aspergillus terreus Thorn. var terreus World J. Microbiol. Biotechnol. 21 2005 1067 1075
    • (2005) World J. Microbiol. Biotechnol. , vol.21 , pp. 1067-1075
    • Cazar, M.E.1    Schmeda-Hirschmann, G.2    Astudillo, L.3
  • 7
    • 0033760789 scopus 로고    scopus 로고
    • Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics
    • P.M. Fischer, and D.P. Lane Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics Curr. Med. Chem. 7 2000 1213 1245
    • (2000) Curr. Med. Chem. , vol.7 , pp. 1213-1245
    • Fischer, P.M.1    Lane, D.P.2
  • 8
    • 0141958932 scopus 로고    scopus 로고
    • Further meroterpenes produced by Penicillium sp., an endophyte obtained from Melia azedarach
    • R.M. Geris dos Santos, and E. Rodrigues-Fo Further meroterpenes produced by Penicillium sp., an endophyte obtained from Melia azedarach Z. Naturforsch. 58c 2003 663 669
    • (2003) Z. Naturforsch. , vol.58 C , pp. 663-669
    • Geris dos Santos, R.M.1    Rodrigues-Fo, E.2
  • 9
    • 33645978063 scopus 로고    scopus 로고
    • Natural products from plant-associated microorganisms: Distribution, diversity, bioactivity, and implications of their occurrence
    • A.A.L. Gunatilaka Natural products from plant-associated microorganisms: distribution, diversity, bioactivity, and implications of their occurrence J. Nat. Prod. 69 2006 509 526
    • (2006) J. Nat. Prod. , vol.69 , pp. 509-526
    • Gunatilaka, A.A.L.1
  • 10
    • 0020286754 scopus 로고
    • Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4α-methyl sterols from the tunicate ascidia nigra
    • T.B.T. Ha, W.C.M.C. Kokke, and C. Djerassl Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4α-methyl sterols from the tunicate ascidia nigra Steroids 40 1982 3041 3053
    • (1982) Steroids , vol.40 , pp. 3041-3053
    • Ha, T.B.T.1    Kokke, W.C.M.C.2    Djerassl, C.3
  • 12
    • 84924961894 scopus 로고    scopus 로고
    • Aegyptolidines A and B: New pyrrolidine alkaloids from the fungus Aspergillus aegyptiacus
    • S.R.M. Ibrahim, G.A. Mohamed, A.M. Moharram, and D.T.A. Youssef Aegyptolidines A and B: new pyrrolidine alkaloids from the fungus Aspergillus aegyptiacus Phytochem. Lett. 12 2015 90 93
    • (2015) Phytochem. Lett. , vol.12 , pp. 90-93
    • Ibrahim, S.R.M.1    Mohamed, G.A.2    Moharram, A.M.3    Youssef, D.T.A.4
  • 13
    • 84858987904 scopus 로고    scopus 로고
    • New constituents from the rhizomes of Egyptian Iris germanica L
    • S.R.M. Ibrahim, G.A. Mohamed, and N.M. Al-Musayeib New constituents from the rhizomes of Egyptian Iris germanica L Molecules 17 2012 2587 2598
    • (2012) Molecules , vol.17 , pp. 2587-2598
    • Ibrahim, S.R.M.1    Mohamed, G.A.2    Al-Musayeib, N.M.3
  • 15
    • 0026571156 scopus 로고
    • Marine sterols XXII. Occurrence of 3-oxo-4,6,8(14)-triunsaturated sterols in the sponge Dysidea herbacea
    • M. Kobayashi, M.M. Krishna, K. Ishida, and V. Anjaneyulu Marine sterols XXII. Occurrence of 3-oxo-4,6,8(14)-triunsaturated sterols in the sponge Dysidea herbacea Chem. Pharm. Bull. 40 1992 72 74
    • (1992) Chem. Pharm. Bull. , vol.40 , pp. 72-74
    • Kobayashi, M.1    Krishna, M.M.2    Ishida, K.3    Anjaneyulu, V.4
  • 16
    • 24744438666 scopus 로고    scopus 로고
    • Sesterterpenoids, terretonins A-D, and an alkaloid, asterrelenin, from Aspergillus terreus
    • G. Li, B. Li, T. Yang, J. Yin, H. Qi, G. Liu, and G. Zhang Sesterterpenoids, terretonins A-D, and an alkaloid, asterrelenin, from Aspergillus terreus J. Nat. Prod. 68 2005 1243 1246
    • (2005) J. Nat. Prod. , vol.68 , pp. 1243-1246
    • Li, G.1    Li, B.2    Yang, T.3    Yin, J.4    Qi, H.5    Liu, G.6    Zhang, G.7
  • 17
    • 84870869424 scopus 로고    scopus 로고
    • Terretonin, ophiobolin, and drimane terpenes with absolute configurations from an algicolous Aspergillus ustus
    • X. Liu, F. Miao, M. Qiao, R.H. Cichewicz, and N. Ji Terretonin, ophiobolin, and drimane terpenes with absolute configurations from an algicolous Aspergillus ustus RSC Adv. 3 2013 588 595
    • (2013) RSC Adv. , vol.3 , pp. 588-595
    • Liu, X.1    Miao, F.2    Qiao, M.3    Cichewicz, R.H.4    Ji, N.5
  • 18
    • 57249097123 scopus 로고    scopus 로고
    • Developing Aspergillus as a host for heterologous expression
    • D. Lubertozzi, and J.D. Keasling Developing Aspergillus as a host for heterologous expression Biotechnol. Adv. 27 2009 53 75
    • (2009) Biotechnol. Adv. , vol.27 , pp. 53-75
    • Lubertozzi, D.1    Keasling, J.D.2
  • 20
    • 0020580209 scopus 로고
    • Metabolic products of Aspergillus terreus. IX. Biosynthesis of butyrolactone derivatives isolated from strain IFO 8835 and 4100
    • K. Nitta, N. Fujita, T. Yoshimura, K. Arai, and Y. Yamamoto Metabolic products of Aspergillus terreus. IX. Biosynthesis of butyrolactone derivatives isolated from strain IFO 8835 and 4100 Chem. Pharm. Bull. 31 1983 1528 1533
    • (1983) Chem. Pharm. Bull. , vol.31 , pp. 1528-1533
    • Nitta, K.1    Fujita, N.2    Yoshimura, T.3    Arai, K.4    Yamamoto, Y.5
  • 22
    • 84919797555 scopus 로고    scopus 로고
    • Territrem and butyrolactone gerivatives from a marine-derived fungus Aspergillus terreus
    • X. Nong, Y. Wang, X. Zhang, M. Zhou, X. Xu, and S. Qi Territrem and butyrolactone gerivatives from a marine-derived fungus Aspergillus terreus Mar. Drugs 12 2014 6113 6124
    • (2014) Mar. Drugs , vol.12 , pp. 6113-6124
    • Nong, X.1    Wang, Y.2    Zhang, X.3    Zhou, M.4    Xu, X.5    Qi, S.6
  • 23
    • 77956329640 scopus 로고    scopus 로고
    • Butenolide and furandione from an endophytic Aspergillus terreus
    • P. Nuclear, D. Sommit, N. Boonyuen, and K. Pudhom Butenolide and furandione from an endophytic Aspergillus terreus Chem. Pharm. Bull. 58 2010 1221 1223
    • (2010) Chem. Pharm. Bull. , vol.58 , pp. 1221-1223
    • Nuclear, P.1    Sommit, D.2    Boonyuen, N.3    Pudhom, K.4
  • 24
    • 59049098123 scopus 로고    scopus 로고
    • Aspernolides A and B, butenolides from a marine-derived fungus Aspergillus terreus
    • R.R. Parvatkar, C. D′souza, A. Tripathi, and C.G. Naik Aspernolides A and B, butenolides from a marine-derived fungus Aspergillus terreus Phytochemistry 70 2009 128 132
    • (2009) Phytochemistry , vol.70 , pp. 128-132
    • Parvatkar, R.R.1    Dsouza, C.2    Tripathi, A.3    Naik, C.G.4
  • 26
    • 79251472417 scopus 로고    scopus 로고
    • Secondary metabolites of fungi from marine habitats
    • M.E. Rateb, and R. Ebel Secondary metabolites of fungi from marine habitats Nat. Prod. Rep. 28 2011 290 344
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 290-344
    • Rateb, M.E.1    Ebel, R.2
  • 28
    • 0031710279 scopus 로고    scopus 로고
    • Effect of butyrolactone i on the producing fungus, Aspergillus terreus
    • T.G. Schimmel, A.D. Coffman, and J. Parsons Effect of butyrolactone I on the producing fungus, Aspergillus terreus Appl. Environ. Microbiol. 64 1998 3707 3712
    • (1998) Appl. Environ. Microbiol. , vol.64 , pp. 3707-3712
    • Schimmel, T.G.1    Coffman, A.D.2    Parsons, J.3
  • 29
    • 0036753195 scopus 로고    scopus 로고
    • Endophytic fungi: A source of biologically active secondary metabolites
    • B. Schulz, C. Boyle, S. Draeger, A.K. Rommert, and K. Krohn Endophytic fungi: a source of biologically active secondary metabolites Mycol. Res. 106 2002 996 1004
    • (2002) Mycol. Res. , vol.106 , pp. 996-1004
    • Schulz, B.1    Boyle, C.2    Draeger, S.3    Rommert, A.K.4    Krohn, K.5
  • 30
    • 0000661423 scopus 로고
    • Terretonin, a toxic compound from Aspergillus terreus
    • J.P. Springer, J.W. Dorner, R.J. Cole, and R.H. Cox Terretonin, a toxic compound from Aspergillus terreus J. Org. Chem. 44 1979 4852 4854
    • (1979) J. Org. Chem. , vol.44 , pp. 4852-4854
    • Springer, J.P.1    Dorner, J.W.2    Cole, R.J.3    Cox, R.H.4
  • 31
  • 32
    • 0038367945 scopus 로고    scopus 로고
    • Endophytes as sources of bioactive products
    • G.A. Strobel Endophytes as sources of bioactive products Microbes Infect. 5 2003 535 544
    • (2003) Microbes Infect. , vol.5 , pp. 535-544
    • Strobel, G.A.1
  • 33
    • 77951610234 scopus 로고    scopus 로고
    • Soyabean lipooxygenase inhibitory and DPPH radical-scavenging activities of aspernolide A and butyrolactones i and II
    • Y. Sugiyama, K. Yoshida, N. Abe, and A. Hirota Soyabean lipooxygenase inhibitory and DPPH radical-scavenging activities of aspernolide A and butyrolactones I and II Biosci. Biotechnol. Biochem. 74 2010 881 883
    • (2010) Biosci. Biotechnol. Biochem. , vol.74 , pp. 881-883
    • Sugiyama, Y.1    Yoshida, K.2    Abe, N.3    Hirota, A.4
  • 34
    • 79960278230 scopus 로고
    • Sterols and other unsaponifiable substances in fats of shell fishes, Crustacea and Eshynodermata. X. Corbisterol
    • Y. Toyama, M. Kita, and T. Tanaka Sterols and other unsaponifiable substances in fats of shell fishes, Crustacea and Eshynodermata. X. Corbisterol J. Chem. Soc. Jpn. 25 1952 355 357
    • (1952) J. Chem. Soc. Jpn. , vol.25 , pp. 355-357
    • Toyama, Y.1    Kita, M.2    Tanaka, T.3
  • 35
    • 80052216478 scopus 로고    scopus 로고
    • Three new compounds from Aspergillus terreus PT06-2 grown in a high salt medium
    • Y. Wang, J. Zheng, P. Liu, and Zhu W. Wang W Three new compounds from Aspergillus terreus PT06-2 grown in a high salt medium Mar. Drugs 9 2011 1368 1378
    • (2011) Mar. Drugs , vol.9 , pp. 1368-1378
    • Wang, Y.1    Zheng, J.2    Liu, P.3    Wang, W.Z.W.4
  • 37
    • 33748991468 scopus 로고    scopus 로고
    • Biology and chemistry of endophytes
    • H.W. Zhang, Y.C. Song, and R.X. Tan Biology and chemistry of endophytes Nat. Prod. Rep. 23 2006 753 771
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 753-771
    • Zhang, H.W.1    Song, Y.C.2    Tan, R.X.3
  • 38
    • 84923918558 scopus 로고    scopus 로고
    • Butyrolactones from the endophytic fungus Aspergillus versicolor and their anti-tobacco mosaic virus activity
    • M. Zhou, J. Lou, Y. Li, Y. Wang, K. Zhou, B. Ji, W. Dong, X. Gao, G. Du, and Q. Hu Butyrolactones from the endophytic fungus Aspergillus versicolor and their anti-tobacco mosaic virus activity J. Braz. Chem. Soc. 26 2015 545 549
    • (2015) J. Braz. Chem. Soc. , vol.26 , pp. 545-549
    • Zhou, M.1    Lou, J.2    Li, Y.3    Wang, Y.4    Zhou, K.5    Ji, B.6    Dong, W.7    Gao, X.8    Du, G.9    Hu, Q.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.