Abstract
The global prevalence of diabetes is likely to increase sharply from 171 million in 2000 and 366 million in 2030. This clearly depicts the frailty of the existing medication for treating diabetes. Organic compounds, especially Schiff bases, flaunt anti-diabetic effects specifically for type 2 diabetes mellitus (T2DM). The research work demonstrates the synthesis of 4-Hydroxy-3-methoxybenzaldehyde Schiff bases following green chemistry and substantiates its activity against T2DM using in silico methods. All the three Schiff bases provide evidence for insulysin inhibition with Pa values more than 0.6 with strict adherence to Lipinski’s rule. Insulysin or insulin-degrading enzyme is a zinc metalloprotease involved in the degradation of insulin and is signified to be a diabetes susceptibility gene. Molecular docking studies with the synthesized Schiff bases against insulysin (3E4A) reveal that compounds S2 and S3 exhibit better binding and affinity than the natural inhibitor ML345.
Original language | English |
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Pages (from-to) | 63-71 |
Number of pages | 9 |
Journal | Journal of Applied Pharmaceutical Science |
Volume | 11 |
Issue number | 7 |
Early online date | 12 Jun 2021 |
DOIs | |
Publication status | Published - Jul 2021 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2021. Sridevi Chigurupati et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
Keywords
- activity prediction
- diabetes
- Insulin degradation
- molecular docking
- Schiff base
ASJC Scopus subject areas
- Medicine (miscellaneous)
- General Pharmacology, Toxicology and Pharmaceutics
- Pharmacology (medical)