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Details

Autor(en) / Beteiligte
Titel
Design, synthesis, in silico , and in vitro evaluation of benzylbenzimidazolone derivatives as potential drugs on α-glucosidase and glucokinase as pharmacological targets
Ist Teil von
  • RSC advances, 2023-07, Vol.13 (31), p.21153-21162
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2023
Link zum Volltext
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • Benzimidazolones have shown biological activities, including antihyperglycemic and hypoglycemic, by inhibiting or activating of α-glu and GK. The aim of this study is the rational design of compounds using assays to delimitate the selection of structures to synthesize and the evaluation of benzimidazolone derivatives in blood glucose control. A docking of 23 benzimidazolone derivatives was performed; selecting the compounds with better profiles to synthesize by microwave-irradiation/conventional heat and evaluate in enzymatic evaluation. Compounds 2k, 2m, 2r, and 2s presented the best profiles, showing good affinity energy (-10.9 to -8.6 kcal mol ) and binding with catalytic-amino acids. They were synthesized at 70 °C and 24 h using DMF as the solvent and potassium carbonate (yield: 22-38%). The results with α-glu showed moderate inhibition of 2k (14 ± 1.23-29 ± 0.45), 2m (12 ± 2.21-36 ± 0.30), 2r (7 ± 2.21-13 ± 1.34), and 2s (11 ± 0.74-35 ± 2.95) at evaluated concentrations (0.1 to 100 μg mL ). The GK activation assay showed an enzymatic activity increase; compound 2k increased 1.31 and 2.83 more than normal activity, 2m (2.13-fold), 2s (2.86 and 3.74-fold) at 100 and 200 μg mL respectively. The present study showed that the 2s derivative presents moderate potential as an α-glu inhibitor and a good activator potential of GK, suggesting that this compound is a good candidate for blood glucose control through antihyperglycemic and hypoglycemic mechanisms.
Sprache
Englisch
Identifikatoren
ISSN: 2046-2069
eISSN: 2046-2069
DOI: 10.1039/d3ra02916f
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10337652

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