Issue 63, 2014

Identification of novel inhibitors that disrupt STAT3–DNA interaction from a γ-AApeptide OBOC combinatorial library

Abstract

From a γ-AApeptide-based one-bead-one-compound (OBOC) combinatorial library, we identified γ-AApeptides that can selectively inhibit STAT3–DNA interaction and suppress the expression levels of STAT3 target genes in intact cells. Our results demonstrate that in addition to the SH2 domain, the DNA binding domain of STAT3 is targetable for the development of a new generation of anti-cancer therapeutics.

Graphical abstract: Identification of novel inhibitors that disrupt STAT3–DNA interaction from a γ-AApeptide OBOC combinatorial library

Supplementary files

Article information

Article type
Communication
Submitted
22 May 2014
Accepted
09 Jun 2014
First published
09 Jun 2014

Chem. Commun., 2014,50, 8739-8742

Author version available

Identification of novel inhibitors that disrupt STAT3–DNA interaction from a γ-AApeptide OBOC combinatorial library

P. Teng, X. Zhang, H. Wu, Q. Qiao, S. M. Sebti and J. Cai, Chem. Commun., 2014, 50, 8739 DOI: 10.1039/C4CC03909B

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