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Volumn 3, Issue 7, 2005, Pages 1172-1173

Bassianolone: An antimicrobial precursor of cephalosporolides E and F from the entomoparasitic fungus Beauveria bassiana

Author keywords

[No Author keywords available]

Indexed keywords

BIOCATALYSTS; BIOSYNTHESIS; DNA; HYDROLYSIS; KETONES; METABOLISM; METABOLITES; MIXTURES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTONS; SIGNAL PROCESSING; STEREOCHEMISTRY; STRUCTURE (COMPOSITION);

EID: 17544379745     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b417534d     Document Type: Article
Times cited : (48)

References (25)
  • 4
    • 0347694375 scopus 로고    scopus 로고
    • and previous issues in this series
    • M. Gill, Nat. Prod Rep., 2003, 20, 615 and previous issues in this series.
    • (2003) Nat. Prod Rep. , vol.20 , pp. 615
    • Gill, M.1
  • 12
    • 0347627366 scopus 로고    scopus 로고
    • and references therein
    • For previously described metabolites from this fungus, see: H. Kikuchi, N. Takahashi and Y. Oshima, Tetrahedron Lett., 2004, 45, 367 and references therein.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 367
    • Kikuchi, H.1    Takahashi, N.2    Oshima, Y.3
  • 13
    • 17544375180 scopus 로고    scopus 로고
    • note
    • 1.
  • 14
    • 17544371890 scopus 로고    scopus 로고
    • note
    • 1.
  • 15
    • 17544381304 scopus 로고    scopus 로고
    • note
    • 5Na requires 239.0895).
  • 16
    • 17544366801 scopus 로고    scopus 로고
    • note
    • 3CO), 206.7 (C-6). NMR peak assignments were made with the aid of 2D NMR experiments (COSY, HMQC and HMBC). The numbering system follows that employed in ref. 1 for cephalosporolides E and F.
  • 18
    • 17544363287 scopus 로고    scopus 로고
    • note
    • 4 requires 198.0892).
  • 19
    • 17544375753 scopus 로고    scopus 로고
    • note
    • 3) 23.6 (q), 24.5 (t), 34.1 (t), 37.5 (t), 52.3 (q), 67.4 (d), 106.0 (d), 108.7 (d), 145.9 (s), 155.5 (s), 170.2 (s).
  • 20
    • 17544374436 scopus 로고    scopus 로고
    • note
    • 1.
  • 21
    • 0021921867 scopus 로고
    • The biosynthesis of various families of sesquiterpene lactones with different carbon skeletons (eudesmanolides, guaianolides, elemanolides, etc) from germacranolides as common precursors is one of the most intriguing examples; for a review including synthesis and biology of sesquiterpene lactones see: H. M. R. Hoffmann and J. Rabe, Angew. Chem. Int. Ed. Engl., 1985, 24, 94.
    • (1985) Angew. Chem. Int. Ed. Engl. , vol.24 , pp. 94
    • Hoffmann, H.M.R.1    Rabe, J.2
  • 23
    • 17544373214 scopus 로고    scopus 로고
    • National Committee for Clinical Laboratory Standards. Approved standard M7-A2, Villanova, Pa, USA, 1990. Approved standard M27-A, Wayne, Pa, USA, 1997
    • National Committee for Clinical Laboratory Standards. Approved standard M7-A2, Villanova, Pa, USA, 1990. Approved standard M27-A, Wayne, Pa, USA, 1997.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.