Back to Search
Start Over
Dihydroquinazolin-4(1H)-one derivatives as novel and potential leads for diabetic management
- Source :
- Molecular Diversity. 26:849-868
- Publication Year :
- 2021
- Publisher :
- Springer Science and Business Media LLC, 2021.
-
Abstract
- A variety of dihydroquinazolin-4(1H)-one derivatives (1–37) were synthesized via “one-pot” three-component reaction scheme by treating aniline and different aromatic aldehydes with isatoic anhydride in the presence of acetic acid. Chemical structures of compounds were deduced by different spectroscopic techniques including EI-MS, HREI-MS, 1H-, and 13C-NMR. Compounds were subjected to α-amylase and α-glucosidase inhibitory activities. A number of derivatives exhibited significant to moderate inhibition potential against α-amylase (IC50 = 23.33 ± 0.02—88.65 ± 0.23 μM) and α-glucosidase (IC50 = 25.01 ± 0.12—89.99 ± 0.09 μM) enzymes, respectively. Results were compared with the standard acarbose (IC50 = 17.08 ± 0.07 μM for α-amylase and IC50 = 17.67 ± 0.09 μM for α-glucosidase). Structure–activity relationship (SAR) was rationalized by analyzing the substituents effects on inhibitory potential. Kinetic studies were implemented to find the mode of inhibition by compounds which revealed competitive inhibition for α-amylase and non-competitive inhibition for α-glucosidase. However, in silico study identified several important binding interactions of ligands (synthetic analogues) with the active site of both enzymes.
- Subjects :
- chemistry.chemical_classification
biology
In silico
Organic Chemistry
Active site
General Medicine
Combinatorial chemistry
Catalysis
Inorganic Chemistry
chemistry.chemical_compound
Acetic acid
Non-competitive inhibition
Aniline
Enzyme
chemistry
Drug Discovery
biology.protein
medicine
Physical and Theoretical Chemistry
Molecular Biology
Quinazolinone
Information Systems
Acarbose
medicine.drug
Subjects
Details
- ISSN :
- 1573501X and 13811991
- Volume :
- 26
- Database :
- OpenAIRE
- Journal :
- Molecular Diversity
- Accession number :
- edsair.doi...........4c1e406111c497e54cf2938582ccb001