Design and synthesis of sulfonyl-substituted 4,5-diarylthiazoles as selective cyclooxygenase-2 inhibitors-Reference-Cited by-同舟云学术

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Design and synthesis of sulfonyl-substituted 4,5-diarylthiazoles as selective cyclooxygenase-2 inhibitors

Published:1999-04 Issue:8 Volume:9 Page:1167-1170
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Carter Jeffery S.,Rogier D.J.,Graneto Matthew J.,Seibert Karen,Koboldt Carol M.,Yan Zhang ,Talley John J.

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. Identification of a pharmacologically distinct prostaglandin H synthase in cultured epithelial cells.

2. A serum- and glucocorticoid-regulated 4-kilobase mRNA encodes a cyclooxygenase-related protein.

3. Differential inhibition of prostaglandin endoperoxide synthase (cyclooxygenase) isozymes by aspirin and other non-steroidal anti-inflammatory drugs.

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1. Classification of Cyclooxygenase-2 Inhibitors Using Support Vector Machine and Random Forest Methods;Journal of Chemical Information and Modeling;2019-02-14

2. Rational Use of Heterogeneous Data in Quantitative Structure–Activity Relationship (QSAR) Modeling of Cyclooxygenase/Lipoxygenase Inhibitors;Journal of Chemical Information and Modeling;2019-01-28

3. Medicinal chemistry of vicinal diaryl scaffold: A mini review;European Journal of Medicinal Chemistry;2019-01

4. Synthesis of Heterocycles from Thioamides;Chemistry of Thioamides;2019

5. SAR and QSAR models of cyclooxygenase-1 (COX-1) inhibitors;SAR and QSAR in Environmental Research;2018-10-02

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