| Literature DB >> 31132600 |
Vrinda Sharma1, Parth Bhatia1, Ozair Alam2, Mohd Javed Naim1, Farah Nawaz1, Aadil Ahmad Sheikh1, Mukund Jha1.
Abstract
Cyclooxygenase-2 is a very important physiological enzyme playing key roles in various biological functions especially in the mechanism of pain and inflammation, among other roles, making it a molecule of high interest to the pharmaceutical community as a target. COX 2 enzyme is induced only during inflammatory processes or cancer and reflects no role in the guarding stomach lining. Thus, selective COX-2 inhibition can significantly reduce the adverse effects including GI tract damage and hepatotoxic effects of traditional NSAIDs like aspirin, ibuprofen, etc. Recent developments on COX-2 inhibitors is primarily focused on improving the selectivity index of the drug towards COX-2 along with enhancing the potency of the drug by modifying the scaffolds of Coxibs currently in the market like Celecoxib, Indomethacin, Oxaprozin, etc. We have reported the progress on new COX-2 inhibitors in the last decade (2008-2019) focussing on five heterocyclic rings- Pyrazole, Indole, Oxazole, Pyridine and Pyrrole. The addition of various moieties to these core rings and their structure-activity relationship along with their molecular modelling data have been explored in the article. This review aims to aid medicinal chemists in the design and discovery of better COX-2 inhibitors constructed on these five heterocyclic pharmacophores.Entities:
Keywords: COX-2; Indole; Oxazole; Pyrazole; SAR
Year: 2019 PMID: 31132600 DOI: 10.1016/j.bioorg.2019.103007
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275