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PMID: 12612644 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

The development of COX2 inhibitors.

Nature reviews. Drug discovery ·Vol. 2 ·No. 3 ·2003-03-00 ·Pages 179-91

Flower RJ

Abstract

Aspirin, arguably the world's favourite drug, has been around since the late nineteenth century, but it wasn't until the late 1970s that its ability to inhibit prostaglandin production by the cyclooxygenase enzyme was identified as the basis of its therapeutic action. Early hints of a second form of the cyclooxygenase that was differentially sensitive to other aspirin-like drugs ultimately ushered in an exciting era of drug discovery, culminating in the introduction of an entirely new generation of anti-inflammatories. This article reviews the story of this discovery and looks at the future of cyclooxygenase pharmacology.

MeSH Terms
Animals Anti-Inflammatory Agents, Non-Steroidal/pharmacology Cyclooxygenase 1 Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Cyclooxygenase Inhibitors/pharmacology Drug Design Humans Isoenzymes/metabolism,physiology Membrane Proteins Prostaglandin-Endoperoxide Synthases/metabolism,physiology Structure-Activity Relationship
Chemicals
Anti-Inflammatory Agents, Non-Steroidal Cyclooxygenase 2 Inhibitors Cyclooxygenase Inhibitors Isoenzymes Membrane Proteins Cyclooxygenase 1 Cyclooxygenase 2 PTGS1 protein, human PTGS2 protein, human Prostaglandin-Endoperoxide Synthases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Flower Rod J
Department of Biochemical Pharmacology, The William Harvey Research Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK. r.j.flower@mds.qmul.ac.uk
Article Info
Journal
Nature reviews. Drug discovery
Abbr.
Nat Rev Drug Discov
ISSN
1474-1776
Published
2003-03-00
Pages
179-91
Language
English
Region
England
NLM ID
101124171
Subset
IM
Corrections
CommentIn
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