Synthesis, Cyclooxygenase Inhibition, Anti-Inflammatory Evaluation, and Ulcerogenic Liability of New 1,3,5-Triarylpyrazoline Derivatives Possessing a Methanesulfonyl Pharmacophore-Reference-Cited by-同舟云学术

Synthesis, Cyclooxygenase Inhibition, Anti-Inflammatory Evaluation, and Ulcerogenic Liability of New 1,3,5-Triarylpyrazoline Derivatives Possessing a Methanesulfonyl Pharmacophore

Published:2016-09-07 Issue:10 Volume:349 Page:801-807
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Arch. Pharm. Chem. Life Sci.

Author:

Abdellatif Khaled R. A.¹,Fadaly Wael A. A.¹,Azouz Amany A.²

Affiliation:

1. Department of Pharmaceutical Organic Chemistry; Beni-Suef University; Beni-Suef Egypt

2. Faculty of Pharmacy, Department of Pharmacology and Toxicology; Beni-Suef University; Beni-Suef Egypt

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

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2. Synthesis and Activity of a New Methoxytetrahydropyran Derivative as Dual Cyclooxygenase-2/5-Lipoxygenase Inhibitor

3. Structural Approaches to Explain the Selectivity of COX-2 Inhibitors: Is There a Common Pharmacophore?

4. Selectivity of nonsteroidal antiinflammatory drugs as inhibitors of constitutive and inducible cyclooxygenase.

5. A Novel COX-2 Inhibitor Pyrazole Derivative Proven Effective as an Anti-Inflammatory and Analgesic Drug

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