Design, synthesis and biological potential of 5-(2-amino-6-(3/4-bromophenyl)pyrimidin-4-yl)benzene-1,3-diol scaffolds as promising antimicrobial and anticancer agents

• Published in: Mini-Reviews in Medicinal Chemistry
• Main Author: Kumar S.; Narasimhan B.; Lim S.M.; Ramasamy K.; Mani V.; Ali Shah S.A.
• Format: Article
• Language: English
• Published: Bentham Science Publishers 2019
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85068842264&doi=10.2174%2f1389557518666181009141924&partnerID=40&md5=15282a5b736b19b3d0801edc3433f426
• ISSN: 13895575
• DOI: 10.2174/1389557518666181009141924

Background: A series of 5-(2-amino-6-(3/4-bromophenyl)pyrimidin-4-yl)benzene-1,3-diol scaffolds was synthesized by Claisen-Schmidt condensation and characterized by NMR, IR, Mass and elemental analyses. Methods: The synthesized pyrimidine scaffolds were screened for their antimicrobial activity by tube dilution method as well for antiproliferative activity (human colorectal (HCT116) cancer cell line) by SRB assay. Results: The antimicrobial screening results demonstrated that compounds, k6, k12, k14 and k20 were found to be the most potent ones against selected microbial species. The anticancer screening results indicated that compounds, k8 and k14 displayed potent anticancer activity against cancer cell line (HCT116). Conclusion: Further, the molecular docking study carried to find out the interaction between active pyrimidine compounds with CDK-8 protein indicated that compound k14 showed best dock score with better potency within the ATP binding pocket and may be used as a lead for rational drug designing of the anticancer molecule. © 2019 Mini-Reviews in Medicinal Chemistry. All rights reserved.