| Literature DB >> 20363633 |
William Vernier1, Wesley Chong, David Rewolinski, Samantha Greasley, Thomas Pauly, Morena Shaw, Dac Dinh, Rose Ann Ferre, James W Meador, Seiji Nukui, Martha Ornelas, Robert L Paz, Eric Reyner.
Abstract
A novel series of potent thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV was discovered using structure-based drug design. Synthesis, structure-activity relationship, and optimization of physicochemical properties are described. Low nanomolar potency was achieved, and selected compounds with improved thermodynamic solubility showed promising in vitro inhibition of carbonic anhydrase activity in rabbit iris ciliary body homogenate. (c) 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20363633 DOI: 10.1016/j.bmc.2010.03.014
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641