New phenolic cinnamic acid derivatives as selective COX-2 inhibitors. Design, synthesis, biological activity and structure-activity relationships-Reference-Cited by-同舟云学术

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New phenolic cinnamic acid derivatives as selective COX-2 inhibitors. Design, synthesis, biological activity and structure-activity relationships

Published:2019-10 Issue: Volume:91 Page:103179
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Ribeiro Daniela,Proença Carina,Varela Carla,Janela João,Tavares da Silva Elisiário J.,Fernandes Eduarda,Roleira Fernanda M.F.

Funder

Fundação para a Ciência e a Tecnologia

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference28 articles.

1. TIS10, a phorbol ester tumor promoter-inducible mRNA from Swiss 3T3 cells, encodes a novel prostaglandin synthase/cyclooxygenase homologue;Kujubu;J. Biol. Chem.,1991

2. Systematic study of constitutive cyclooxygenase-2 expression: Role of NF-κB and NFAT transcriptional pathways;Kirkby;Proc. Natl. Acad. Sci.,2016

3. Biological basis for the cardiovascular consequences of COX-2 inhibition: therapeutic challenges and opportunities;Grosser;J. Clin. Invest.,2006

4. The effect of COX-2-selective meloxicam on the myocardial, vascular and renal risks: a systematic review;Asghar;Inflammopharmacology,2015

5. Cyclooxygenase inhibitors: From pharmacology to clinical read-outs;Patrignani;Biochim Biophys Acta,1851

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