Biscoumarin-1,2,3-triazole hybrids as novel anti-diabetic agents: Design, synthesis, in vitro α-glucosidase inhibition, kinetic, and docking studies.

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ID: 14076
2019
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Abstract
A novel series of biscoumarin-1,2,3-triazole hybrids 6a-n was prepared and evaluated for α-glucosidase inhibitory potential. All fourteen derivatives exhibited excellent α-glucosidase inhibitory activity with IC values ranging between 13.0 ± 1.5 and 75.5 ± 7.0 µM when compared with the acarbose as standard inhibitor (IC = 750.0 ± 12.0 µM). Among the synthesized compounds, compounds 6c (IC = 13.0 ± 1.5 µM) and 6g (IC = 16.4 ± 1.7 µM) exhibited the highest inhibitory activity against α-glucosidase and were non-cytotoxic towards normal fibroblast cells. Kinetic study revealed that compound 6c inhibits the α-glucosidase in a competitive mode. Furthermore, molecular docking investigation was performed to find interaction modes of the biscoumarin-1,2,3-triazole derivatives.
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asgari2019biscoumarin123triazolebioorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Asgari, Mohammad Sadegh;Mohammadi-Khanaposhtani, Maryam;Kiani, Mitra;Ranjbar, Parviz Rashidi;Zabihi, Ebrahim;Pourbagher, Roghayeh;Rahimi, Rahmatollah;Faramarzi, Mohammad Ali;Biglar, Mahmood;Larijani, Bagher;Mahdavi, Mohammad;Hamedifar, Haleh;Hajimiri, Mir Hamed;
Journal Bioorganic chemistry
Year 2019
DOI
S0045-2068(19)30895-8
URL
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