Design, synthesis and therapeutic potential of 3-(2-(1H-benzo[d]imidazol-2-ylthio)acetamido)-N-(substituted phenyl)benzamide analogues

• Published in: Chemistry Central Journal
• 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. 2018
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85058978808&doi=10.1186%2fs13065-018-0513-3&partnerID=40&md5=6fa10fee7720fcd4795cd9e39ccbbc4a

Background: The emergence of bacterial resistance is a major public health problem. It is essential to develop and synthesize new therapeutic agents with better activity. The mode of actions of certain newly developed antimicrobial agents, however, exhibited very limited effect in treating life threatening systemic infections. Therefore, the advancement of multi-potent and efficient antimicrobial agents is crucial to overcome the increased multi-drug resistance of bacteria and fungi. Cancer, which remains as one of the primary causes of deaths and is commonly treated by chemotherapeutic agents, is also in need of novel and efficacious agents to treat resistant cases. As such, a sequence of novel substituted benzamides was designed, synthesized and evaluated for their antimicrobial and anticancer activities. Methodology: All synthesized compounds were characterized by IR, NMR, Mass and elemental analysis followed by in vitro antimicrobial studies against Gram-positive (Staphylococcus aureus), Gram-negative (Salmonella typhi and Klebsiella pneumoniae) bacterial and fungal (Candida albicans and Aspergillus niger) strains by the tube dilution method. The in vitro anticancer evaluation was carried out against the human colorectal carcinoma cell line (HCT116), using the Sulforhodamine B assay. Results, discussion and conclusion: Compound W6 (MIC sa, st, kp = 5.19 μM) emerged as a significant antibacterial agent against all tested bacterial strains i.e. Gram-positive (S. aureus), Gram-negative (S. typhi, K. pneumoniae) while compound W1 (MIC ca, an = 5.08 μM) was most potent against fungal strains (A. niger and C. albicans) and comparable to fluconazole (MIC = 8.16 μM). The anticancer screening demonstrated that compound W17 (IC50 = 4.12 μM) was most potent amongst the synthesized compounds and also more potent than the standard drug 5-FU (IC50 = 7.69 μM). [Figure not available: see fulltext.] © 2018 The Author(s).