Literature DB >> 11392547

Thiazole analogues of the NSAID indomethacin as selective COX-2 inhibitors.

K W Woods1, R W McCroskey, M R Michaelides, C K Wada, K I Hulkower, R L Bell.   

Abstract

The carboxyl group of the NSAID indomethacin was replaced with a variety of substituted thiazoles to obtain a series of potent, selective inhibitors of COX-2. Additional substitutions were made at the 1-position and 5-position of the indole of indomethacin.

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Year:  2001        PMID: 11392547     DOI: 10.1016/s0960-894x(01)00212-8

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  4 in total

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Journal:  Int J Mol Sci       Date:  2020-06-29       Impact factor: 5.923

Review 2.  Thiazoles and Thiazolidinones as COX/LOX Inhibitors.

Authors:  Konstantinos Liaras; Maria Fesatidou; Athina Geronikaki
Journal:  Molecules       Date:  2018-03-18       Impact factor: 4.411

Review 3.  An Overview of the Synthesis and Antimicrobial, Antiprotozoal, and Antitumor Activity of Thiazole and Bisthiazole Derivatives.

Authors:  Anca-Maria Borcea; Ioana Ionuț; Ovidiu Crișan; Ovidiu Oniga
Journal:  Molecules       Date:  2021-01-25       Impact factor: 4.411

4.  Drug Design, Synthesis and Biological Evaluation of Heterocyclic Molecules as Anti-Inflammatory Agents.

Authors:  Jignasa Savjani; Bhavesh Variya; Snehal Patel; Suja Mulamkattil; Harsh Amin; Shital Butani; Ahmed Allam; Jamaan Ajarem; Harsh Shah
Journal:  Molecules       Date:  2022-02-14       Impact factor: 4.411

  4 in total

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