Literature DB >> 18220987

Current status of COX-2 inhibitors.

Palwinder Singh1, Anu Mittal.   

Abstract

The two isoforms of enzyme cyclooxygenase viz. COX-1 and COX-2 play key roles in the metabolism of arachidonic acid. The enzyme COX-2, when over expressed, leads to more production of prostaglandins causing inflammation and it also participates in the propagation of cancer. Therefore, COX-2 becomes the cellular target of a number of chemical entities for the treatment of inflammatory diseases as well as for the chemotherapy of cancer. In the present review, an up to date status of the compounds investigated for COX-2 inhibition has been given so that a collective view of the existing COX-2 inhibitors could be helpful for the design of safer anti-inflammatory drugs. In order to cover the maximum reported COX-2 inhibitors, a unique classification on the basis of the central core of the molecule (carrying mostly the phenyl moieties) has been followed, an outline of which has been given below: [structure: see text]. Each category of compounds has been discussed with suitable examples giving the IC(50) (for COX-2) values and the selectivity towards COX-2 over COX-1 of most potent compounds.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18220987     DOI: 10.2174/138955708783331577

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  6 in total

1.  Anti-cancer effects of celecoxib on nasopharyngeal carcinoma HNE-1 cells expressing COX-2 oncoprotein.

Authors:  Jiongyu Chen; Yonggang Ran; Chaoqun Hong; Zhijian Chen; Yanjie You
Journal:  Cytotechnology       Date:  2010-09-01       Impact factor: 2.058

2.  Acanthopanax koreanum fruit waste inhibits lipopolysaccharide-induced production of nitric oxide and prostaglandin E2 in RAW 264.7 macrophages.

Authors:  Eun-Jin Yang; Ji-Young Moon; Jung-Soon Lee; Jaesook Koh; Nam Ho Lee; Chang-Gu Hyun
Journal:  J Biomed Biotechnol       Date:  2010-03-23

3.  Novel valdecoxib derivatives by ruthenium(ii)-promoted 1,3-dipolar cycloaddition of nitrile oxides with alkynes - synthesis and COX-2 inhibition activity.

Authors:  Silvia Roscales; Nicole Bechmann; Daniel Holger Weiss; Martin Köckerling; Jens Pietzsch; Torsten Kniess
Journal:  Medchemcomm       Date:  2018-02-13       Impact factor: 3.597

4.  Studies of synthetic chalcone derivatives as potential inhibitors of secretory phospholipase A2, cyclooxygenases, lipoxygenase and pro-inflammatory cytokines.

Authors:  Ibrahim Jantan; Syed Nasir Abbas Bukhari; Olayiwola A Adekoya; Ingebrigt Sylte
Journal:  Drug Des Devel Ther       Date:  2014-09-16       Impact factor: 4.162

5.  PPARs Mediate Lipid Signaling in Inflammation and Cancer.

Authors:  Liliane Michalik; Walter Wahli
Journal:  PPAR Res       Date:  2008-12-21       Impact factor: 4.964

6.  Synergy of Physico-chemical and Biological Experiments for Developing a Cyclooxygenase-2 Inhibitor.

Authors:  Palwinder Singh; Jagroop Kaur; Harpreet Kaur; Anudeep Kaur; Rajbir Bhatti
Journal:  Sci Rep       Date:  2018-07-03       Impact factor: 4.379

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.