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α-Glucosidase, α-Amylase and Antioxidant Evaluations of Isolated Bioactives from Wild Strawberry. | LitMetric

AI Article Synopsis

  • Diabetes mellitus is a major global health issue, prompting research to find antidiabetic bioactive compounds from specific plant sources.
  • Various plant extracts were tested in laboratory assays for their ability to inhibit enzymes related to glucose metabolism, finding ethyl acetate to be the most effective fraction.
  • Two promising compounds were isolated and characterized, demonstrating strong inhibitory effects on α-glucosidase and α-amylase, potentially paving the way for further animal studies on their antidiabetic properties.

Article Abstract

Diabetes mellitus is a metabolic disorder and is a global challenge to the current medicinal chemists and pharmacologists. This research has been designed to isolate and evaluate antidiabetic bioactives from . The crude extracts, semi-purified and pure bioactives have been used in all in vitro assays. The in vitro α-glucosidase, α-amylase and DPPH free radical activities have been performed on all plant samples. The initial activities showed that ethyl acetate () was the potent fraction in all the assays. This fraction was initially semi-purified to obtain -. Among the semi-purified fractions, was dominant, exhibiting potent IC values in all the in vitro assays. Based on the potency and availability of materials, was subjected to further purification to obtain compounds (2,4-dichloro-6-hydroxy-3,5-dimethoxytoluene) and (2-methyl-6-(4-methylphenyl)-2-hepten-4-one). The two isolated compounds were characterized by mass and NMR analyses. The compounds and showed excellent inhibitions against α-glucosidase (21.45 for and 15.03 for μg/mL), α-amylase (17.65 and 16.56 μg/mL) and DPPH free radicals (7.62 and 14.30 μg/mL). Our study provides baseline research for the antidiabetic bioactives exploration from . The bioactive compounds can be evaluated in animals-based antidiabetic activity in future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182347PMC
http://dx.doi.org/10.3390/molecules27113444DOI Listing

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