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Volumn 52, Issue 39, 1996, Pages 12651-12666

Novel mammalian cell cycle inhibitors, spirotryprostatins A and B, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; SPIROTRYPROSTATIN A; SPIROTRYPROSTATIN B; UNCLASSIFIED DRUG;

EID: 0030599282     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00737-5     Document Type: Article
Times cited : (543)

References (24)
  • 1
    • 0011843656 scopus 로고    scopus 로고
    • in press
    • 1. A part of this work was reported in our preliminary communication. C.-B. Cui, H. Kakeya and H. Osada, J. Antibiot., 1996, 49 (8), in press.
    • (1996) J. Antibiot. , vol.49 , Issue.8
    • Cui, C.-B.1    Kakeya, H.2    Osada, H.3
  • 3
    • 0026337295 scopus 로고
    • 3. R. A. Weinberg, Science, 1991, 254, 1138-1146.
    • (1991) Science , vol.254 , pp. 1138-1146
    • Weinberg, R.A.1
  • 11
    • 85030272750 scopus 로고    scopus 로고
    • note
    • 13C NMR signal patterns comparing with those of 1. For instance, two amide carbonyl carbons in the diketopiperazine part in 2 appeared in the markedly high field region (δ162.60, C-11 and δ155.09, C-17) than the corresponding carbons in 1 (Table 2), tryprostatins and related diketopiperazine alkaloids (cf. reference 9).
  • 18
    • 85030274418 scopus 로고    scopus 로고
    • note
    • CH coupling constant of the C-8 methine group.
  • 19
  • 24
    • 85030277613 scopus 로고    scopus 로고
    • note
    • 9 positions between 1 and 2 might be involved except for the effect of methoxy group in 1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.