4-(2-(1H-Benzo[d]imidazol-2-ylthio) acetamido)-N-(substituted phenyl)benzamides: Design, synthesis and biological evaluation

• Published in: BMC Chemistry
• Main Author: Tahlan S.; Ramasamy K.; Lim S.M.; Shah S.A.A.; Mani V.; Narasimhan B.
• Format: Article
• Language: English
• Published: BioMed Central Ltd 2019
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85091148352&doi=10.1186%2fs13065-019-0533-7&partnerID=40&md5=dd621e6f2c49c8b9aca88b36cdd71944

Background: Dihydrofolate reductase (DHFR) is an important target for antimetabolite class of antimicrobials because it participates in purine synthesis. 2-mercaptobenzimidazole (2MBI) has similar structural features as purine nucleotides. Given that benzimidazole and similar heteroaromatics have been broadly examined for their anticancer potential, so, we hereby report the design, synthesis and biological studies (i.e. antimicrobial and anticancer studies) of 2MBI derivatives. Methodology: The antimicrobial activity of synthesized 2MBI derivatives were evaluated against Gram positive and Gram negative bacterial species as well as fungal species by tube dilution technique whereas their anticancer activity was assessed against human colorectal carcinoma cell line (HCT116) by Sulforhodamine B (SRB) assay. They were also structurally characterized by IR, NMR, MS and elemental analyses. Results, discussion and conclusion: The antimicrobial activity findings revealed that compound N1 ( MICbs,st,ca = 1.27, 2.54, 1.27 uM), N8 ( MICec= 1.43 uM), N22 ( MICkp,an= 2.60 uM), N23 and N25 ( MICsa= 2.65 uM) exhibited significant antimicrobial effects against tested strains, i.e. Gram-positive, Gram-negative (bacterial) and fungal strains. The anticancer screening results demonstrated that compounds N9, N18 ( IC50 = 5.85, 4.53 uM) were the most potent compounds against cancer cell line (HCT116) even more than 5-FU, the standard drug ( IC50 = 9.99 uM). © 2019 BioMed Central Ltd.. All rights reserved.