Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1253, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2021.132266
Keywords
Antidiabetic; Thiadiazole; Metal complexes; DFT; Molecular docking; EDAX
Categories
Funding
- CSIR-New Delhi [09/752(0087)/2018-EMR-I]
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A new series of transition metal complexes were synthesized and characterized, showing good biological activity and potential as orally active drugs. Docking studies of the potent compounds revealed their activity in the active sites of human pancreatic alpha-amylase and alpha-glucosidase.
A new series of transition metal complexes of type [M(L1-3)(H2O)(CH3COO)] where, M = Co(II), Ni(II), Cu(II) & Zn(II), and L1 = 2-(((1,3,4-thiadiazol-2-yl)imino)methyl)-6-ethoxyphenol; L-2 = 2-ethoxy-6-(((5-methyl-1,3,4-thiadiazol-2-yl)imino)methyl)phenol; L-3 = 2-ethoxy-6-(((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)imino)methyl)phenol; were synthesized and characterized by various spectral and physico-analytical techniques such as H-1, (CNMR)-C-13, FTIR, HRMS, XRD, ESR, TGA, SEM and EDAX. The studies envisaged a penta-coordinated geometry for the complexes, where the Schiffbase ligands act in a tridentate manner via the azomethine nitrogen, deprotonated oxygen and one of the nitrogen atom of thiadiazole heterocycle. DFT/B3LYP theoretical method was utilised for calculations of molecular electrostatic potential, HUMO-LUMO energy values of selected compounds. In an in-vitro experiment, the antidiabetic effects of the synthesized compounds were assessed on alpha-amylase and alpha-glucosidase enzymes. It was found that compounds 14 and 15 revealed good biological potency with IC50 value close to Acarbose (standard). In-silico study of the synthesized compounds was carried out to check the drug-likeness and it was observed that compounds can be used as orally active drugs. Additionally, molecular docking studies of the potent compounds i.e. 14 and 15, were carried out in the active site of human pancreatic alpha-amylase (PDB code: 1BSI) and alpha-glucosidase (PDB code: 5ZCC). (C) 2021 Elsevier B.V. All rights reserved.
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