Synthesis and cytotoxic evaluation of α-methylene-γ-butyrolactone bearing naphthalene and naphtho[2,1-b]furan derivatives

被引:50
|
作者
Lee, KH
Huang, BR
机构
[1] Tajen Inst Technol, Dept Pharm, Pingtung, Taiwan
[2] Kaohsiung Med Univ, Sch Chem, Kaohsiung 807, Taiwan
关键词
cytotoxicity; naphtho[2,1-b]furan; naphthalene; alpha-methlene-gamma-butyrolactone;
D O I
10.1016/S0223-5234(02)01354-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Naphthalene alpha-methlene-gamma-butyrolactones exhibits a unique cytotoxicity profile. They are highly cytostatic for leukaemia cancer cells but are not cytocidal. For almost all the solid tumours tested. they are both cytostatic and cytocidal. Substitution of a bromo atom on either naphthalene or both naphthalene and gamma-phenyl moiety of the lactone enhanced potency while retaining the same cytotoxicity profile. The tricyclic naphtho[2.1-b]furan derivatives. prepared from 2-hydroxy-1-naphthaldehyde in an efficient pathway, also possess the same cytotoxicity profile. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:333 / 338
页数:6
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