Abstract |
Cyclooxygenase (COX) inhibitors are widely used analgesic and anti-inflammatory drugs. Owing to undesirable effects caused by unselective COX inhibitors and selective COX-2 inhibitors, microsomal prostaglandin E(2) synthase-1 has been considered as an alternative target for the development of analgesic drugs. However, recent findings question the usefulness of this terminal synthase as a promising drug target for pain therapy.
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Authors | Klaus Scholich, Gerd Geisslinger |
Journal | Trends in pharmacological sciences
(Trends Pharmacol Sci)
Vol. 27
Issue 8
Pg. 399-401
(Aug 2006)
ISSN: 0165-6147 [Print] England |
PMID | 16815559
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Cyclooxygenase Inhibitors
- Intramolecular Oxidoreductases
- PTGES protein, human
- Prostaglandin-E Synthases
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Topics |
- Animals
- Cyclooxygenase Inhibitors
(pharmacology, therapeutic use)
- Humans
- Intramolecular Oxidoreductases
(antagonists & inhibitors, metabolism)
- Models, Biological
- Pain
(drug therapy, enzymology)
- Prostaglandin-E Synthases
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