Article ID Journal Published Year Pages File Type
10594189 Bioorganic & Medicinal Chemistry Letters 2012 4 Pages PDF
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.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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