메뉴 건너뛰기




Volumn 72, Issue 18, 2011, Pages 2406-2412

Isolation, structure elucidation and biological activity of metabolites from Sch-642305-producing endophytic fungus Phomopsis sp. CMU-LMA

Author keywords

Anticancer; Antimicrobial; Phomopsis; Polyketides; Secondary metabolites

Indexed keywords

MACROLIDE; POLYKETIDE; SCH 642305;

EID: 80054953379     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2011.08.010     Document Type: Article
Times cited : (32)

References (29)
  • 2
    • 0032101350 scopus 로고    scopus 로고
    • A hydroxytetradecatrienoic acid from Mycosphaerella rubella
    • DOI 10.1016/S0031-9422(98)00027-2, PII S0031942298000272
    • A. Arnone, G. Nasini, and O. Vajna de Pava A hydroxytetradecatrienoic acid from Mycosphaerella rubella Phytochemistry 48 1998 507 510 (Pubitemid 28285109)
    • (1998) Phytochemistry , vol.48 , Issue.3 , pp. 507-510
    • Arnone, A.1    Nasini, G.2    Vajna De Pava, O.3
  • 3
    • 0034018458 scopus 로고    scopus 로고
    • Structure and biosynthesis of mutolide, a novel macrolide from a UV mutant of the fungus F-249707
    • H.B. Bode, M. Walker, and A. Zeeck Structure and biosynthesis of mutolide, a novel macrolide from a UV mutant of the fungus F-249707 Eur. J. Org. Chem. 2000 2000 1451 1456
    • (2000) Eur. J. Org. Chem. , vol.2000 , pp. 1451-1456
    • Bode, H.B.1    Walker, M.2    Zeeck, A.3
  • 6
    • 67650661399 scopus 로고    scopus 로고
    • A radical mediated approach to the stereoselective formal total synthesis of (+)-Sch 642305
    • T.K. Chakraborty, R. Samanta, and P.K. Kumar A radical mediated approach to the stereoselective formal total synthesis of (+)-Sch 642305 Tetrahedron 65 2009 6925 6931
    • (2009) Tetrahedron , vol.65 , pp. 6925-6931
    • Chakraborty, T.K.1    Samanta, R.2    Kumar, P.K.3
  • 8
    • 38349089002 scopus 로고    scopus 로고
    • New perspective for natural products synthesis: Concise synthesis of (+)-sch 642305 by chiral auxiliary multiuse methodology
    • H. Fujioka, Y. Ohba, K. Nakahara, M. Takatsuji, K. Murai, M. Ito, and Y. Kita New perspective for natural products synthesis: concise synthesis of (+)-sch 642305 by chiral auxiliary multiuse methodology Org. Lett. 9 2007 5605 5608
    • (2007) Org. Lett. , vol.9 , pp. 5605-5608
    • Fujioka, H.1    Ohba, Y.2    Nakahara, K.3    Takatsuji, M.4    Murai, K.5    Ito, M.6    Kita, Y.7
  • 9
    • 35348948949 scopus 로고    scopus 로고
    • Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer
    • DOI 10.1016/j.tet.2007.09.080, PII S0040402007016705
    • J. García-Fortanet, M. Carda, and J.A. Marco Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer Tetrahedron 63 2007 12131 12137 (Pubitemid 47600291)
    • (2007) Tetrahedron , vol.63 , Issue.49 , pp. 12131-12137
    • Garcia-Fortanet, J.1    Carda, M.2    Alberto Marco, J.3
  • 10
    • 42049089524 scopus 로고    scopus 로고
    • Chemistry and weak antimicrobial activities of phomopsins produced by mangrove endophytic fungus Phomopsis sp. ZSU-H76
    • Z. Huang, X. Cai, C. Shao, Z. She, X. Xia, Y. Chen, J. Yang, S. Zhou, and Y. Lin Chemistry and weak antimicrobial activities of phomopsins produced by mangrove endophytic fungus Phomopsis sp. ZSU-H76 Phytochemistry 69 2008 1604 1608
    • (2008) Phytochemistry , vol.69 , pp. 1604-1608
    • Huang, Z.1    Cai, X.2    Shao, C.3    She, Z.4    Xia, X.5    Chen, Y.6    Yang, J.7    Zhou, S.8    Lin, Y.9
  • 11
    • 32444438179 scopus 로고    scopus 로고
    • Stereoselective synthesis of Sch 642305, an inhibitor of bacterial DNA primase
    • DOI 10.1016/j.tet.2005.12.009, PII S0040402005021563
    • K. Ishigami, and R. Katsuta Stereoselective synthesis of Sch 642305, an inhibitor of bacterial DNA primase Tetrahedron 62 2006 2224 2230 (Pubitemid 43227896)
    • (2006) Tetrahedron , vol.62 , Issue.10 , pp. 2224-2230
    • Ishigami, K.1    Katsuta, R.2    Watanabe, H.3
  • 12
    • 67149144494 scopus 로고    scopus 로고
    • Synthetic studies of natural 10-membered lactones, mueggelone, microcarpalide, and sch 642305, which have interesting bioactivities
    • K. Ishigami Synthetic studies of natural 10-membered lactones, mueggelone, microcarpalide, and sch 642305, which have interesting bioactivities Biosci. Biotechnol. Biochem. 73 2009 971 979
    • (2009) Biosci. Biotechnol. Biochem. , vol.73 , pp. 971-979
    • Ishigami, K.1
  • 13
    • 0029140830 scopus 로고
    • A new hydroxytetradecatrienoic acid and its glyceryl esters from valsa ambiens
    • Y. Jiao, T. Yoshihara, M. Akimoto, and A. Ichihara A new hydroxytetradecatrienoic acid and its glyceryl esters from valsa ambiens Phytochemistry 38 1995 419 422
    • (1995) Phytochemistry , vol.38 , pp. 419-422
    • Jiao, Y.1    Yoshihara, T.2    Akimoto, M.3    Ichihara, A.4
  • 15
    • 54149092551 scopus 로고    scopus 로고
    • Evolving trends in the dereplication of natural product extracts: New methodology for rapid, small-scale investigation of natural product extracts
    • G. Lang, N.A. Mayhudin, M.I. Mitova, L. Sun, S. Van Der Sar, J.W. Blunt, A.L. Cole, G. Ellis, H. Laatsch, and M.H. Munro Evolving trends in the dereplication of natural product extracts: new methodology for rapid, small-scale investigation of natural product extracts J. Nat. Prod. 71 2008 1595 1599
    • (2008) J. Nat. Prod. , vol.71 , pp. 1595-1599
    • Lang, G.1    Mayhudin, N.A.2    Mitova, M.I.3    Sun, L.4    Van Der Sar, S.5    Blunt, J.W.6    Cole, A.L.7    Ellis, G.8    Laatsch, H.9    Munro, M.H.10
  • 16
    • 37549045968 scopus 로고    scopus 로고
    • A-seco-oleane-type triterpenes from Phomopsis sp. (strain HKI0458) isolated from the mangrove plant Hibiscus tiliaceus
    • L. Li, I. Sattler, Z. Deng, I. Groth, G. Walther, M. Klaus-Dieter, G. Peschel, S. Grabley, and W. Lin A-seco-oleane-type triterpenes from Phomopsis sp. (strain HKI0458) isolated from the mangrove plant Hibiscus tiliaceus Phytochemistry 69 2008 511 517
    • (2008) Phytochemistry , vol.69 , pp. 511-517
    • Li, L.1    Sattler, I.2    Deng, Z.3    Groth, I.4    Walther, G.5    Klaus-Dieter, M.6    Peschel, G.7    Grabley, S.8    Lin, W.9
  • 17
    • 54449088219 scopus 로고    scopus 로고
    • One new ten-membered lactone from Phomopsis sp. B27, an endophytic fungus of Annona squamosa L
    • X. Lin, C.H. Lu, and Y.M. Shen One new ten-membered lactone from Phomopsis sp. B27, an endophytic fungus of Annona squamosa L Chinese Journal of Natural Medicines 6 2008 391 394
    • (2008) Chinese Journal of Natural Medicines , vol.6 , pp. 391-394
    • Lin, X.1    Lu, C.H.2    Shen, Y.M.3
  • 18
    • 23644431505 scopus 로고    scopus 로고
    • Enantioselective total synthesis of bioactive natural product (+)-Sch 642305: A structurally novel inhibitor of bacterial DNA primase and HIV-1 Tat transactivation
    • DOI 10.1039/b505264e
    • G. Mehta, and H.M. Shinde Enantioselective total synthesis of bioactive natural product (+)-Sch 642305: a structurally novel inhibitor of bacterial DNA primase and HIV-1 Tat transactivation Chem. Commun. 7 2005 3703 3705 (Pubitemid 41133153)
    • (2005) Chemical Communications , Issue.29 , pp. 3703-3705
    • Mehta, G.1    Shinde, H.M.2
  • 19
    • 23944503279 scopus 로고    scopus 로고
    • Enantioselective synthesis of epi-(+)-Sch 642305: Observation of an interesting diastereoselection during RCM
    • DOI 10.1016/j.tetlet.2005.07.152, PII S004040390501693X
    • G. Mehta, and H.M. Shinde Enantioselective synthesis of epi-(+)-Sch 642305: observation of an interesting diastereoselection during RCM Tetrahedron Lett. 46 2005 6633 6636 (Pubitemid 41207139)
    • (2005) Tetrahedron Letters , vol.46 , Issue.39 , pp. 6633-6636
    • Mehta, G.1    Shinde, H.M.2
  • 20
    • 34248197054 scopus 로고    scopus 로고
    • Production and fungitoxic activity of Sch 642305, a secondary metabolite of Penicillium canescens
    • DOI 10.1007/s11046-007-9015-x
    • R. Nicoletti, M.P. Lopez-Gresa, E. Manzo, A. Carella, and M.L. Ciavatta Production and fungitoxic activity of Sch 642305, a secondary metabolite of Penicillium canescens Mycopathologia 163 2007 295 301 (Pubitemid 46717953)
    • (2007) Mycopathologia , vol.163 , Issue.5 , pp. 295-301
    • Nicoletti, R.1    Lopez-Gresa, M.P.2    Manzo, E.3    Carella, A.4    Ciavatta, M.L.5
  • 23
    • 66149162958 scopus 로고    scopus 로고
    • A chemoenzymatic asymmetric synthesis of methyl (6S, 13R)-6, 13-dihydroxytetradeca-(2E, 4E, 8E)-trienoate, a component of Mycosphaerella rubella
    • A. Sharma, S. Gamre, and S. Chattopadhyay A chemoenzymatic asymmetric synthesis of methyl (6S, 13R)-6, 13-dihydroxytetradeca-(2E, 4E, 8E)-trienoate, a component of Mycosphaerella rubella Tetrahedron: Asymmetry 20 2009 1164 1167
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1164-1167
    • Sharma, A.1    Gamre, S.2    Chattopadhyay, S.3
  • 24
    • 33645900581 scopus 로고    scopus 로고
    • Synthesis of (+)-Sch 642305 by a biomimetic transannular Michael reaction
    • DOI 10.1021/ol052948+
    • B.B. Snider, and J. Zhou Synthesis of (+)-sch 642305 by a biomimetic transannular Michael reaction Org. Lett. 8 2006 1283 1286 (Pubitemid 43587421)
    • (2006) Organic Letters , vol.8 , Issue.7 , pp. 1283-1286
    • Snider, B.B.1    Zhou, J.2
  • 26
    • 63149095536 scopus 로고    scopus 로고
    • Molecular phylogeny of Magnaporthaceae (Sordariomycetes) with a new species Ophioceras chiangdaoense from Dracaena loureiroi in Thailand
    • S. Thongkantha, R. Jeewon, D. Vijaykrishna, S. Lumyong, E.H.C. McKenzie, and K.D. Hyde Molecular phylogeny of Magnaporthaceae (Sordariomycetes) with a new species Ophioceras chiangdaoense from Dracaena loureiroi in Thailand Fungal Diversity 34 2009 157 173
    • (2009) Fungal Diversity , vol.34 , pp. 157-173
    • Thongkantha, S.1    Jeewon, R.2    Vijaykrishna, D.3    Lumyong, S.4    McKenzie, E.H.C.5    Hyde, K.D.6
  • 27
    • 0032506582 scopus 로고    scopus 로고
    • Isolation, structural determination, and total synthesis of a new biologically active δ-lactone produced by Seiridium unicorne
    • PII S0040403998021030
    • H. Toshima, A. Watanabe, H. Sato, and A. Ichihara Isolation, Structural Determination, and Total Synthesis of A New Biologically Active 8-Lactone Produced by Seiridium unicorne Tetrahedron Lett. 39 1998 9223 9226 (Pubitemid 28539270)
    • (1998) Tetrahedron Letters , vol.39 , Issue.50 , pp. 9223-9226
    • Toshima, H.1    Watanabe, A.2    Sato, H.3    Ichihara, A.4
  • 28
    • 34147112254 scopus 로고    scopus 로고
    • Concise synthesis of the bacterial DNA primase inhibitor (+) -Sch 642305
    • E.M. Wilson, and D. Trauner Concise synthesis of the bacterial DNA primase inhibitor (+) -Sch 642305 Org. Lett. 9 2007 1327 1329
    • (2007) Org. Lett. , vol.9 , pp. 1327-1329
    • Wilson, E.M.1    Trauner, D.2
  • 29
    • 53649108134 scopus 로고    scopus 로고
    • Phomoeuphorbins A-D, azaphilones from the fungus Phomopsis euphorbiae
    • B.Z. Yu, G.H. Zhang, Z.Z. Du, Y.T. Zheng, J.C. Xu, and X.D. Luo Phomoeuphorbins A-D, azaphilones from the fungus Phomopsis euphorbiae Phytochemistry 69 2008 2523 2526
    • (2008) Phytochemistry , vol.69 , pp. 2523-2526
    • Yu, B.Z.1    Zhang, G.H.2    Du, Z.Z.3    Zheng, Y.T.4    Xu, J.C.5    Luo, X.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.