4.7 Article

Synthesis of 1-benzyl-3-(5-hydroxymethyl-2-furyl)selenolo[3,2-c]pyrazole derivatives as new anticancer agents

期刊

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 45, 期 4, 页码 1395-1402

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2009.12.039

关键词

Selenolopyrazole; Thienopyrazole; Furopyrazole; YC-1 analogs; Structure-activity relationships (SAR); Cytotoxicity

资金

  1. National Science Council of the Republic of China [NSC 96-2628-B039-001, NSC 97-2320-B-039-003-MY3]

向作者/读者索取更多资源

As part of our continuing search for potential anticancer drug candidates among YC-1 analogs, 1,3-disubstituted selenolo[3,2-c]pyrazole derivatives were synthesized and evaluated for their cytotoxicity against NCI-H226 non-small cell lung cancer and A-498 renal cancer cell lines. Significant cytotoxicity was observed in 3-(5-hydroxymethy1-2-furyl) derivatives (2, 33, 36 and 37). Among them, compound 2 was found to have the most potent activity. The mode of action of compound 2 seems to differ from those of the 175 anticancer agents listed in NCI's standard database and resembles that of YC-1. Thus, we recommend that compound 2 should be developed further as new drug candidate for treatment of non-small cell lung cancer and renal cancer. (C) 2009 Elsevier Masson SAS. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据