4.5 Article

Synthesis of novel forskolin isoxazole derivatives with potent anti-cancer activity against breast cancer cell lines

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 27, 期 18, 页码 4314-4318

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2017.08.033

关键词

Forskolin; Isoxazoles; Breast cancer; 1,3-Dipolar cycloadditions; Regioselectivity

资金

  1. UGC-New Delhi, India
  2. UGC-FRP, Government of India [F.4-5(136-FRP)/2014 (BSR)]
  3. DST-SERB [EMR/2014/000904]

向作者/读者索取更多资源

Forskolin C-1-isoxazole derivatives (3,5-regioisomers) (11a-e, 14, 15a-h and 15, 16a-g) were synthesized regioselectively by adopting 1,3-dipolar cycloadditions. These derivatives were tested using estrogen receptor positive breast cancer cell lines MCF-7 and BT-474. Majority of the compounds exhibited activity against the p53-positive MCF-7 breast cancer cells but not against the p53-negative BT-474 breast cancer cells. Among forskolin derivatives, compounds 11a, 11c, 14a, 14f, 14g, 14h, 15b, 16g and 17b exhibited higher anti-cancer activity against MCF-7 cell line with an IC50 <= 1 mu M. The derivative 14f exhibited highest activity in both p53-positive (MCF-7) and p53-negative (BT-474) breast cancer cell lines with an IC50 of 0.5 mu M. (C) 2017 Published by Elsevier Ltd.

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

4.5
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