2,2-Dimethyl-4,5-diaryl-3(2 H )furanone derivatives as selective cyclo-oxygenase-2 inhibitors-Reference-Cited by-同舟云学术

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2,2-Dimethyl-4,5-diaryl-3(2 H )furanone derivatives as selective cyclo-oxygenase-2 inhibitors

Published:2001-01 Issue:2 Volume:11 Page:165-168
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shin Song Seok,Noh Min-Soo,Byun Young Joo,Choi Jin Kyu,Kim Ji Young,Lim Kyung Min,Ha Jun-Yong,Kim Jin Kwan,Lee Chang Hoon,Chung Shin

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference18 articles.

1. Human cyclooxygenase-2 cDNA.

2. Pairet, M.; Churchill, L.; Engelhardt, G. In New Targets in Inflammation: Inhibitors of COX-2 or Adhesion Molecules; Bazan, N.; Botting, J.; Vane, J., Eds.; Kluwer Academic: London, 1996; pp 23–38.

3. Chapter 19. Selective Cyclooxygenase Inhibitors

4. Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)

5. The discovery of rofecoxib, [MK 966, VIOXX®, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2 inhibitor

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