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Volumn 46, Issue 8, 1998, Pages 1325-1329

Preparation and structure-activity relationships of novel asterriquinone derivatives

Author keywords

Asterriquinone; Cytotoxicity; Mouse leukemia P388 cell; Partial deacetylation; Structure activity relationship

Indexed keywords

ANTINEOPLASTIC AGENT; ASTERRIQUINONE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0031756308     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.46.1325     Document Type: Article
Times cited : (13)

References (25)
  • 22
    • 0002538947 scopus 로고
    • ed. by Gilman A. G., Rall T. W., Nies A. S., Taylor P., Pergamon Press, New York
    • a) Calabresi P., Chabner B. A., "Pharmacologic Basis of Therapeutics," ed. by Gilman A. G., Rall T. W., Nies A. S., Taylor P., Pergamon Press, New York, 1990, pp. 1202-1263;
    • (1990) Pharmacologic Basis of Therapeutics , pp. 1202-1263
    • Calabresi, P.1    Chabner, B.A.2
  • 24
    • 3542991545 scopus 로고    scopus 로고
    • note
    • 2b) the total amount of 1a and 3a per 12 1 medium were 730 mg and 36 mg, respectively. In this study, using modified malt extract medium [malt extract, 20g; glucose, 20 g; polypepton Y® (Wako Pure Chemical Industries, Ltd.), 8g; tap water 11], 1a (1063mg) and 3a (155 mg) were obtained in good yield.
  • 25
    • 3543002965 scopus 로고
    • Ph. D. Thesis, Kyoto University, Kyoto, Japan
    • Arai K., Ph. D. Thesis, Kyoto University, Kyoto, Japan, 1984.
    • (1984)
    • Arai, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.