Unknown

Dataset Information

0

Discovery of Novel Coumarin Analogs against the ?-Glucosidase Protein Target of Diabetes Mellitus: Pharmacophore-Based QSAR, Docking, and Molecular Dynamics Simulation Studies.


ABSTRACT: Diabetes mellitus (DM) is a chronic metabolic disease, the third killer of mankind. The finding of potent drugs against diabetes remains challenging. In the present study, coumarin derivatives with known biological activity against diabetic protein have been used to predict functional groups' positions on coumarin derivatives. ?-Glucosidase is a brush border membrane-bound lysosomal enzyme from the hydrolase enzyme family. It plays an important role in the metabolism of glycoproteins. Inhibitors of lysosomal ?-glucosidase can reduce postprandial hyperglycemia. Due to this, lysosomal ?-glucosidase is a good therapeutic target for drugs. A total of 116 coumarin derivatives with IC50 values against lysosomal ?-glucosidase were selected for a CADD (computer-aided drug design) approach to identify more potent drugs. Pharmacophore modeling and atom-based 3-QSAR of 116 active compounds against lysosomal ?-glucosidase were performed and identified positions and types of groups to increase activity. We performed molecular docking of 116 coumarin derivatives against the lysosomal ?-glucosidase enzyme, and three compounds (isorutarine, 10_, and 36) resulted in a docking score of -7.64, -7.12, and -6.86 kcal/mol. The molecular dynamics simulation of the above three molecules and protein complex performed for 100 ns supported the interaction stability of isorutarine, 10_, and 36 with the lysosomal binding site ?-glucosidase.

SUBMITTER: Maurya AK 

PROVIDER: S-EPMC7758891 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Discovery of Novel Coumarin Analogs against the α-Glucosidase Protein Target of Diabetes Mellitus: Pharmacophore-Based QSAR, Docking, and Molecular Dynamics Simulation Studies.

Maurya Akhilesh Kumar AK   Mulpuru Viswajit V   Mishra Nidhi N  

ACS omega 20201210 50


Diabetes mellitus (DM) is a chronic metabolic disease, the third killer of mankind. The finding of potent drugs against diabetes remains challenging. In the present study, coumarin derivatives with known biological activity against diabetic protein have been used to predict functional groups' positions on coumarin derivatives. α-Glucosidase is a brush border membrane-bound lysosomal enzyme from the hydrolase enzyme family. It plays an important role in the metabolism of glycoproteins. Inhibitors  ...[more]

Similar Datasets

| S-EPMC10826614 | biostudies-literature
| S-EPMC10475976 | biostudies-literature
| S-EPMC9913026 | biostudies-literature
| S-EPMC7408124 | biostudies-literature
| S-EPMC3257097 | biostudies-literature
| S-EPMC8047494 | biostudies-literature
| S-EPMC6720998 | biostudies-literature
| S-EPMC10449137 | biostudies-literature
| S-EPMC8040153 | biostudies-literature
| S-EPMC9271751 | biostudies-literature