Chemmedchem 2013-04-01

Benzenesulfonamides: a unique class of chemokine receptor type 4 inhibitors.

Suazette Reid Mooring, Jin Liu, Zhongxing Liang, Jeffrey Ahn, Samuel Hong, Younghyoun Yoon, James P Snyder, Hyunsuk Shim

文献索引：ChemMedChem 8(4) , 622-32, (2013)

全文：HTML全文

摘要

The interaction of CXCR4 with CXCL12 (SDF-1) plays a critical role in cancer metastasis by facilitating the homing of tumor cells to metastatic sites. Based on our previously published work on CXCR4 antagonists, we have synthesized a series of aryl sulfonamides that inhibit the CXCR4/CXCL12 interaction. Analogue bioactivities were assessed with binding affinity and Matrigel invasion assays. Computer modeling was employed to evaluate a selection of the new analogues docked into the CXCR4 X-ray structure and to rationalize discrepancies between the affinity and Matrigel in vitro assays. A lead compound displays nanomolar potency in the binding affinity assay (IC(50)=8.0 nM) and the Matrigel invasion assay (100 % blockade of invasion at 10 nM). These data demonstrate that benzenesulfonamides are a unique class of CXCR4 inhibitors with high potency.Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.