Abstract
Cyclooxygenases are responsible for the biosynthesis of prostanoids, the overt presence of which is often associated with inflammation and pain. Since the discovery of COX-2 in the last decade, a myriad of selective COX-2 inhibitors and their pharmacological profiles have been witnessed. Pharmacological observations of selective inhibition of COX-2 often go beyond initial expectations. This review is an overview of issues on selective COX-2 inhibitors, which include gastrointestinal and cardiovascular safety, emerging therapeutic areas and differentiation in drug profiles expected to be addressed by future generation COX-2 inhibitors. This article also covers recent patents and papers on new COX-2 inhibitors published since 2002. Future generation COX-2 inhibitors are sure to be safer and meet better medical needs than the COX-2 inhibitors currently available for the treatment or prevention of broadly ranged COX-2-mediated disorders.
| Original language | English |
|---|---|
| Pages (from-to) | 9-32 |
| Number of pages | 24 |
| Journal | Expert Opinion on Therapeutic Patents |
| Volume | 15 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2005 |
Bibliographical note
Funding Information:This work was partially supported by a grant of The Korean Health 21 R&D Project (code number: 0405-DD00-0101-003) from Ministry of Health & Welfare, Republic of Korea.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cancer
- Cardiorenal safety
- COX-2
- Cyclooxygenase
- Inflammation
- Pain
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