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ABSTRACT: Background
Presently available chemical based synthetic preservative have emerged with various side effects, so the aspiration of natural and side effect free novel preservative has been greatly increased. As the natural preservative exhibit poor side effect with improved preservative efficacy. The recent development in computational studies leads advancement in drug designing and discovery of novel glucosamine-6-phosphate synthase (G-6-P synthase) inhibition based natural antimicrobial preservatives. Here, selected aesculin derivatives were screened for G-6-P synthase inhibition via docking study and evaluated for antioxidant, antimicrobial, preservative efficacy as well stability study.Results
Modified aesculin derivatives were designed, synthesized and showed potent G-6-
SUBMITTER: Lather A
PROVIDER: S-EPMC8317424 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature