The alpha-glucosidase- and lipase-inhibitory activities of three phenalenones (-) and one phenylpropanoid () from the ethyl acetate extracts of a sp. are described. They represent the first secondary metabolites reported from the genus . Scleroderolide () and sclerodione () exhibited potent α-glucosidase- and porcine-lipase-inhibitory activity during primary screening, with better IC values compared to the positive controls, N-deoxynojirimycin and orlistat. In silico techniques were employed to validate the probable biological targets and elucidate the mechanism of actions of phenalenones and . Both compounds exhibited strong binding affinities to both alpha-glucosidase and porcine lipase through H-bonding and π-π interactions. Interestingly, favorable in silico ADME (absorption, distribution, metabolism, and excretion) properties such as gastrointestinal absorption were also predicted using software.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070682PMC
http://dx.doi.org/10.3390/molecules25040965DOI Listing

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