New selective cyclooxygenase-2 inhibitors from cyclocoumarol: Synthesis, characterization, biological evaluation and molecular modeling-Reference-Cited by-同舟云学术

New selective cyclooxygenase-2 inhibitors from cyclocoumarol: Synthesis, characterization, biological evaluation and molecular modeling

Published:2018-02 Issue: Volume:146 Page:577-587
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Rayar Anita Marie,Lagarde Nathalie^ORCID,Martin Frederique,Blanchard Florent,Liagre Bertrand,Ferroud Clotilde,Zagury Jean-François,Montes Matthieu,Sylla-Iyarreta Veitía Maité^ORCID

Funder

Ministry of National Education, Research and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference28 articles.

1. Anti-inflammatory drugs: new multitarget compounds to face an old problem. the dual inhibition concept;Celotti;Pharmacol. Res.,2001

2. Structural and functional basis of cyclooxygenase inhibition;Blobaum;J. Med. Chem.,2007

3. Cyclooxygenase Isozymes: the biology of prostaglandin synthesis and inhibition;Simmons;Pharmacol. Rev.,2004

4. Adverce effects of nonsteroidal antiinflammatory drugs: an update of gastrointestinal, cardiovascular and renal complications;Harirforoosh;J. Pharm. Pharmaceut. Sci.,2013

5. Update on COX-2 Selective Inhibitors: chemical classification, side effects and their use in cancers and neuronal diseases;Rayar;Curr. Top. Med. Chem.,2017

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