Structural Approaches to Explain the Selectivity of COX-2 Inhibitors: Is There a Common Pharmacophore?

Author(s): G. Dannhardt , S. Laufer .

Journal Name: Current Medicinal Chemistry

Volume 7 , Issue 11 , 2000

Abstract:

The identification and characterisation of the isoenzyme cyclooxygenase 2 (COX-2) stimulated investigations to develop efficient nonsteroidal anti-inflammatory drugs with reduced side effects compared to standard NSAIDs. This review will focus on the structural features needed to achieve COX-2 selectivity. Five structural classes can be identified together with a class bearing little or no resemblance to one another in their molecular structure. The most interesting point is the very distinct structure/activity relationship. On the one hand only minor modifications to a particular compound induce a drastic change in its COX selectivity and on the other hand the structural prerequisites in terms of molecular shape, lipophilicity, electron density, flexibility, polarity and H-bonding dynamics allow a wide range of diversity.

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Article Details

VOLUME: 7
ISSUE: 11
Year: 2000
Page: [1101 - 1112]
Pages: 12
DOI: 10.2174/0929867003374237
Price: $58

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