Antioxidant activity and α-glucosidase inhibitability of Distichochlamys citrea M.F. Newman rhizome fractionated extracts: in vitro and in silico screenings
Distichochlamys citrea M.F. Newman (commonly known as “Black Ginger”) is an endemic plant to Vietnam and has been extensively exploited by folk medication for treatments of infection-related diseases and diabetes. In this work, its rhizomes were subjected to fractionated extraction, phytochemical ex...
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Veröffentlicht in: | Chemical papers 2022-09, Vol.76 (9), p.5655-5675 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Distichochlamys citrea
M.F. Newman (commonly known as “Black Ginger”) is an endemic plant to Vietnam and has been extensively exploited by folk medication for treatments of infection-related diseases and diabetes. In this work, its rhizomes were subjected to fractionated extraction, phytochemical examination, evaluation of antioxidant effect by DDPH free radical neutralization, and inhibitory activity toward
α
-glucosidase. The compositional components were subjected to in silico screening, including density functional theory calculation, molecular docking simulation, physicochemical analysis, and pharmacokinetic regression. In the trials, EtOAc fraction is found as the bioactive part of most effectiveness, regarding both antioxidant effect (IC
50
= 90.27 µg mL
−1
) and
α
-glucosidase inhibitory activity (IC
50
= 115.75 μg mL
−1
). Chemical determination reveals there are 13 components of its composition. DFT-based calculations find no abnormal constraints in their structures. Docking-based simulation provides order of inhibitory effectiveness:
3-P53341
>
12-P53341
>
7-P53341
>
4-P53341
>
11-P53341
>
10-P53341
. QSARIS-based investigations implicate their biocompatibility. ADMET-based regressions indicate that all candidates are generally safe for medicinal applications. The findings would contribute to the basis for further studies on the chemical compositions of
Distichochlamys citrea
and their biological activities. |
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ISSN: | 0366-6352 1336-9075 2585-7290 |
DOI: | 10.1007/s11696-022-02273-2 |