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Volumn 102, Issue , 2015, Pages 101-109

Nodulisporisteroids C-L, new 4-methyl-progesteroid derivatives from Nodulisporium sp.

Author keywords

4 Methyl progesteroid derivatives; Endolichenic fungus; Nodulisporium sp.; Xylariaceae

Indexed keywords

4 METHYLPROGESTEROID DERIVATIVE; ANTINEOPLASTIC AGENT; NODULISPORISTEROID C; NODULISPORISTEROID D; NODULISPORISTEROID E; NODULISPORISTEROID F; NODULISPORISTEROID G; NODULISPORISTEROID H; NODULISPORISTEROID I; NODULISPORISTEROID J; NODULISPORISTEROID K; NODULISPORISTEROID L; PROGESTERONE DERIVATIVE; UNCLASSIFIED DRUG; STEROID;

EID: 84939536796     PISSN: 0039128X     EISSN: 18785867     Source Type: Journal    
DOI: 10.1016/j.steroids.2015.08.004     Document Type: Article
Times cited : (24)

References (17)
  • 1
    • 0036902202 scopus 로고    scopus 로고
    • Big effects from small changes: possible ways to explore nature's chemical diversity
    • H.B. Bode, B. Bethe, R. Hofs, and A. Zeeck Big effects from small changes: possible ways to explore nature's chemical diversity Chembiochem 3 2002 619 627
    • (2002) Chembiochem , vol.3 , pp. 619-627
    • Bode, H.B.1    Bethe, B.2    Hofs, R.3    Zeeck, A.4
  • 2
    • 29044440615 scopus 로고    scopus 로고
    • Using jasplakinolide to turn on pathways that enable the isolation of new chaetoglobosins from Phomospis asparagi
    • O.E. Christian, J. Compton, K.R. Christian, S.L. Mooberry, F.A. Valeriote, and P. Crews Using jasplakinolide to turn on pathways that enable the isolation of new chaetoglobosins from Phomospis asparagi J. Nat. Prod. 68 2005 1592 1597
    • (2005) J. Nat. Prod. , vol.68 , pp. 1592-1597
    • Christian, O.E.1    Compton, J.2    Christian, K.R.3    Mooberry, S.L.4    Valeriote, F.A.5    Crews, P.6
  • 3
    • 66749192010 scopus 로고    scopus 로고
    • Spicochalasin A and new aspochalasins from the marine-derived fungus Spicaria elegans
    • Z.J. Lin, T.J. Zhu, H.J. Wei, G.J. Zhang, H. Wang, and Q.Q. Gu Spicochalasin A and new aspochalasins from the marine-derived fungus Spicaria elegans Eur. J. Org. Chem. 2009 3045 3051
    • (2009) Eur. J. Org. Chem. , pp. 3045-3051
    • Lin, Z.J.1    Zhu, T.J.2    Wei, H.J.3    Zhang, G.J.4    Wang, H.5    Gu, Q.Q.6
  • 4
    • 84903631120 scopus 로고    scopus 로고
    • Caryophyllene sesquiterpenes from the marine-derived fungus Ascotricha sp. ZJ-M-5 by the one strain-many compounds strategy
    • W.J. Wang, D.Y. Li, Y.C. Li, H.M. Hua, E.L. Ma, and Z.L. Li Caryophyllene sesquiterpenes from the marine-derived fungus Ascotricha sp. ZJ-M-5 by the one strain-many compounds strategy J. Nat. Prod. 77 2014 1367 1371
    • (2014) J. Nat. Prod. , vol.77 , pp. 1367-1371
    • Wang, W.J.1    Li, D.Y.2    Li, Y.C.3    Hua, H.M.4    Ma, E.L.5    Li, Z.L.6
  • 5
    • 84861648094 scopus 로고    scopus 로고
    • Photipyrones A and B, new pyrone derivatives from the plant endophytic fungus Pestalotiopsis photiniae
    • G. Ding, Y.X. Qi, S.C. Liu, L.D. Guo, and X.L. Chen Photipyrones A and B, new pyrone derivatives from the plant endophytic fungus Pestalotiopsis photiniae J. Antibiot. 65 2012 271 273
    • (2012) J. Antibiot. , vol.65 , pp. 271-273
    • Ding, G.1    Qi, Y.X.2    Liu, S.C.3    Guo, L.D.4    Chen, X.L.5
  • 7
    • 0035145447 scopus 로고    scopus 로고
    • New co-metabolites of the streptazolin pathway
    • C. Puder, S. Loya, A. Hizi, and A. Zeeck New co-metabolites of the streptazolin pathway J. Nat. Prod. 64 2001 42 45
    • (2001) J. Nat. Prod. , vol.64 , pp. 42-45
    • Puder, C.1    Loya, S.2    Hizi, A.3    Zeeck, A.4
  • 10
    • 77954899900 scopus 로고    scopus 로고
    • Homo- and heptanor-sterols and tremulane sesquiterpenes from cultures of Phellinus igniarius
    • X.L. Wu, S. Lin, C.G. Zhu, Z.G. Yue, Y. Yu, F. Zhao, B. Liu, J.G. Dai, and J.G. Shi Homo- and heptanor-sterols and tremulane sesquiterpenes from cultures of Phellinus igniarius J. Nat. Prod. 73 2010 1294 1300
    • (2010) J. Nat. Prod. , vol.73 , pp. 1294-1300
    • Wu, X.L.1    Lin, S.2    Zhu, C.G.3    Yue, Z.G.4    Yu, Y.5    Zhao, F.6    Liu, B.7    Dai, J.G.8    Shi, J.G.9
  • 12
    • 84885003549 scopus 로고    scopus 로고
    • Caught between triterpene- and steroid-metabolism: 4a-carboxylic pregnane-derivative from the marine alga-derived fungus Phaeosphaeria spartinae
    • M.F. Elsebai, S. Kehraus, and G.M. König Caught between triterpene- and steroid-metabolism: 4a-carboxylic pregnane-derivative from the marine alga-derived fungus Phaeosphaeria spartinae Steroids 78 2013 880 883
    • (2013) Steroids , vol.78 , pp. 880-883
    • Elsebai, M.F.1    Kehraus, S.2    König, G.M.3
  • 16
    • 33646412042 scopus 로고    scopus 로고
    • Cytotoxic biotransformed products from cinobufagin by Mucor spinosus and Aspergillus Niger
    • X.J. He, J.S. Tang, A.M. Qiao, G.H. Wang, M.M. Jiang, R.H. Liu, and X.S. Yao Cytotoxic biotransformed products from cinobufagin by Mucor spinosus and Aspergillus Niger Steroids 71 2006 392 402
    • (2006) Steroids , vol.71 , pp. 392-402
    • He, X.J.1    Tang, J.S.2    Qiao, A.M.3    Wang, G.H.4    Jiang, M.M.5    Liu, R.H.6    Yao, X.S.7
  • 17
    • 0032426171 scopus 로고    scopus 로고
    • The biosynthesis of steroids and triterpenoids
    • G.D. Brown The biosynthesis of steroids and triterpenoids Nat. Prod. Rep. 15 1998 653 696
    • (1998) Nat. Prod. Rep. , vol.15 , pp. 653-696
    • Brown, G.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.