| Literature DB >> 23122522 |
Hou-ling Dai1, Li-xin Gao, Ying Yang, Jing-ya Li, Jia-gao Cheng, Jia Li, Ren Wen, Yan-qing Peng, Jian-bin Zheng.
Abstract
A series of di-indolinone derivatives was designed and synthesized to optimize our lead compounds basing on molecular docking study as PTP1B inhibitors. Successive enzymatic assay identified the synthetic di-indolinone as novel PTP1B inhibitors with low micromole-ranged inhibitory activity and at least several-fold selectivity over other tested homologous PTPs.Entities:
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Year: 2012 PMID: 23122522 DOI: 10.1016/j.bmcl.2012.10.054
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823