Synthesis and antitumour activity of 1H,3H-thiazolo[3,4-a]benzimidazole derivatives

被引：0
|
作者：
Chimirri, A
Monforte, P
Musumeci, L
Rao, A
Zappalà, M
Monforte, AM
机构：
[1] Univ Messina, Dipartimento Farmacochim, I-98168 Messina, Italy
[2] Univ Catanzaro, Dipartimento Sci Farmacobiol, I-88021 Roccelletta Di Borgia, CZ, Italy
来源：
ARCHIV DER PHARMAZIE | 2001年 / 334卷 / 06期
关键词：
1H,3H-thinzolo[3,4-a]benzimidazoles; antitumour activity;
D O I：
10.1002/1521-4184(200106)334:6<203::AID-ARDP203>3.0.CO;2-L
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
A series of 1H,3H-thiazolo[3,4-a]benzimidazoles were synthesized and tested for their in vitro antitumour activity against 60 human tumour cell lines. Some derivatives exhibited both tumour growth inhibition activity and cellular selectivity. In particular, compound 8c, the most active of the series, was very active towards all cell lines at concentrations ranging from 10(-7)-10(-5) M. Compound 4a, on the other hand, was highly selective against the CNS cancer cell line.
引用
收藏
页码：203 / 208
页数：6
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