Inhibitory, biocompatible, and pharmacological potentiality of dammarenolic‐acid derivatives towards α‐glucosidase (3W37) and tyrosine phosphatase 1B(PTP1B)

Dammarenolic‐acid derivatives experimentally demonstrated possessing inhibition activity towards α‐glucosidase might be used as the evidence to retrieve an inhibitory mechanism and subjected for computational screening on other diabetes‐related proteins, e.g. tyrosine phosphatase 1B. Seven structures reported in our preceding work (denoted as 1‐7)were subjected for an in silicoinvestigation in this study on inhibitability towards protein structure PDB‐3W37 by molecular docking simulation. The computer‐based results see a good agreement with those from laboratory‐based reports, with the order of static stability: 3‐3W37> 1‐3W37> 7‐3W37> 2‐3W37> 6‐3W37~ 5‐3W37~ 4‐3W37(negligible activity). Together, experiment‐theory reveals the most promising candidates are 1‐3and 7. The in‐theory order for most promising inhibitors regarding protein structure UniProt‐PTP1B is: 1‐PTP1B> 6‐PTP1B> 4‐PTP1B. Quantity‐structure relationship analyses (i.e. QSARIS and ADMET) expect 1‐3as compounds with sufficient bio‐ and pharma‐compatibility. Altogether, the results specify 1as the most promising candidate for multi‐purpose inhibition towards diabetes‐based proteins, thus encouraging elevated efforts for validation and further development for application.