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ABSTRACT: Objective
The study aimed to synthesize and characterize pyrimidine-linked benzimidazole hybrids, define their antimicrobial and antifungal activities in vitro, and determine their ability to inhibit the main protease and spike glycoprotein of SARS-CoV-2. Methods
The ability of the synthesized compounds to inhibit the main protease and spike glycoprotein inhibitory of SARS-CoV-2 was investigated by assessing their mode of binding to the allosteric site of the enzyme using molecular docking. The structures of pyrimidine-linked benzimidazole derivatives synthesized with microwave assistance were confirmed by spectral analysis. Antibacterial and antifungal activities were determined by broth dilution. Results
Gram-negative bateria (Escherichia coli and Pseudomonas a
SUBMITTER: Khan S
PROVIDER: S-EPMC8274991 | biostudies-literature | 2021 Jun
REPOSITORIES: biostudies-literature