Diaryl indenes and benzofurans: Novel classes of potent and selective cyclooxygenase-2 inhibitors
- 19 October 1995
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 5 (20) , 2377-2380
- https://doi.org/10.1016/0960-894x(95)00414-o
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesionsPublished by Elsevier ,2002
- Selective cyclooxygenase inhibitors: Novel 4-spiro 1,2-diarylcyclopentenes are potent and orally active cox-2 inhibitorsBioorganic & Medicinal Chemistry Letters, 1995
- Expression and selective inhibition of the constitutive and inducible forms of human cyclo-oxygenaseBiochemical Journal, 1995
- Selective Cyclooxygenase Inhibitors: Novel 1,2-Diarylcyclopentenes Are Potent and Orally Active COX-2 InhibitorsJournal of Medicinal Chemistry, 1994
- A novel one-pot conversion of methyl sulfones to sulfonamidesTetrahedron Letters, 1994
- NS-398, a new anti-inflammatory agent, selectively inhibits prostaglandin G/H synthase/cyclooxygenase (COX-2) activity in vitroProstaglandins, 1994
- Gastrointestinal Damage Associated with the Use of Nonsteroidal Antiinflammatory DrugsNew England Journal of Medicine, 1992
- Mechanisms of nonsteroidal anti-inflammatory drug-induced gastric damageThe American Journal of Medicine, 1989
- Ring contraction of 2-chlorocyclohexanone with Grignard reagents.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of BasesSynthetic Communications, 1981