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Volumn , Issue 14, 2004, Pages 2509-2512

20-Deoxy-20-fluorocamptothecin: Design and synthesis of camptothecin isostere

Author keywords

Antitumor agent; Asymmetric synthesis; Camptothecin; Fluorine; Topoisomerase I

Indexed keywords

20 DEOXY 20 FLUOROCAMPTOTHECIN; 20 DEOXYCAMPTOTHECIN; ANTINEOPLASTIC AGENT; BENZENE DERIVATIVE; CAMPTOTHECIN DERIVATIVE; CINCHONA ALKALOID; DNA TOPOISOMERASE; FLUORINE DERIVATIVE; LACTONE DERIVATIVE; N FLUOROBENZENESULFONIMIDE; NATURAL PRODUCT; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 9644302441     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-834810     Document Type: Article
Times cited : (57)

References (51)
  • 24
    • 0034751015 scopus 로고    scopus 로고
    • and references therein
    • The ability of the C-F bond to act as a hydrogen bond acceptor is a matter of considerable debate. It highly depends on the molecular structures. See: Shibata, N.; Das, B. K.; Harada, K.; Takeuchi, Y.; Bando, M. Synlett 2001, 1755; and references therein.
    • (2001) Synlett , pp. 1755
    • Shibata, N.1    Das, B.K.2    Harada, K.3    Takeuchi, Y.4    Bando, M.5
  • 43
    • 9644296500 scopus 로고    scopus 로고
    • note
    • -1 (λ/nm) -0.06 (402.0), -1.88 (360.8), 0 (309.3), +0.32 (304.2), 0 (291.3), -0.08 (288.8), 0 (284.5), +18.2 (232.8),+6.10 (221.0).
  • 51
    • 9644256502 scopus 로고    scopus 로고
    • note
    • In initial cytotoxicity study, both 20(S)- and 20(R)-fluoroCPT (2) were evaluated on three human cancer cell lines (KB, A549 and HT-29) and they appeared to be less active than CPT (1). Further biological study using pure enantiomer of 2 is now under considerations.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.