Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377358 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
A new series of β-N-biaryl ether sulfonamide hydroxamates as novel gelatinase inhibitors is described. These compounds exhibit good potency for MMP-2 and MMP-9 without inhibiting MMP-1. The structure–activity relationships (SAR) reveal the biaryl ether type P1′ moiety together with methanesulfonamide is the optimal combination that provides inhibitory activity of MMP-9 in the single-digit nanomolar range.
Graphical abstractA new series of β-N-biaryl ether sulfonamide hydroxamates as novel gelatinase inhibitors is described.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shyh-Ming Yang, Robert H. Scannevin, Bingbing Wang, Sharon L. Burke, Lawrence J. Wilson, Prabha Karnachi, Kenneth J. Rhodes, Bharat Lagu, William V. Murray,