Design, synthesis, and studies of small molecule STAT3 inhibitors

被引：84

作者：

Bhasin, Deepak ^{[1
]}

Cisek, Katryna ^{[1
]}

Pandharkar, Trupti ^{[1
]}

Regan, Nicholas ^{[1
]}

Li, Chenglong ^{[1
]}

Pandit, Bulbul ^{[1
]}

Lin, Jiayuh ^{[2
]}

Li, Pui-Kai ^{[1
]}

机构：

[1] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA

[2] Ohio State Univ, Columbus Childrens Res Inst, Ctr Childhood Canc, Columbus, OH 43205 USA

来源：

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 2008年 / 18卷 / 01期

关键词：

D O I：

10.1016/j.bmcl.2007.10.031

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

A series of small molecule STAT3 inhibitors originally derived from our lead compound STA 21 were synthesized and evaluated. The most potent compound in this series, compound 1, exhibited the same anti-proliferative activities as STA 21 against prostate cancer cell lines that express constitutively active STAT3. Molecular docking showed compound 1 bound to the STAT3 beta SH2 domain in a similar manner as STA 21. (C) 2007 Elsevier Ltd. All rights reserved.

引用

页码：391 / 395

页数：5

共 31 条

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