Title of article
Chemistry and pharmacokinetics of diarylthiophenes and terphenyls as selective COX-2 inhibitors
Author/Authors
Donald J. P. Pinto، نويسنده , , Robert A. Copeland، نويسنده , , Maryanne B. Covington، نويسنده , , William J. Pitts، نويسنده , , Douglas G. Batt، نويسنده , , Michael J. Orwat، نويسنده , , Gilbert N. Lam، نويسنده , , Amita Joshi، نويسنده , , Yuk-Charn Chan، نويسنده , , Shuaige Wang، نويسنده , , James M. Trzaskos، نويسنده , , Ronald L. Magolda، نويسنده , , David M. Kornhauser، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1996
Pages
6
From page
2907
To page
2912
Abstract
DuP697, 2-bromo-4-(4′-sulfonylmethyl)phenyl-5-(4′-fluoro)phenylthiophene, is a selective type 2 cyclooxygenase (COX-2) inhibitor. Its relatively weak COX-2 selectivity coupled with a poor human pharmacokinetic profile led us to seek improvements on the in vitro selectivity while at the same time, addressing some of its pharmacokinetic liabilities. In this paper we discuss some strategies at solving the PK issue within a class of COX-2 inhibitors. The result of these efforts led to the discovery of a new class of COX-2 inhibitors the terphenyls, which prove to be superior alternatives to the diarylthiophenes.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
1996
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
788464
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