Aug 2026· ACS Omega· Vol 11, pp. 53855 - 53881· 0 citations· 64 references
Medicine
TL;DR
This study establishes a robust design paradigm for the rapid development of highly potent kinase inhibitors through structure-based computational strategies and indicates that 3D-QSAR modeling contributed as a complementary triage tool rather than a standalone driver of lead discovery.
Abstract
Serine/threonine kinase 3 (STK3) is a core kinase in the Hippo signaling pathway that regulates cell proliferation, differentiation, and apoptosis. Dysregulation of this pathway is linked to various cancers and immune disorders, emphasizing STK3 as a promising therapeutic target for diseases that involve abnormal cell growth. Despite their therapeutic relevance, only a limited number of potent STK3 inhibitors have been reported, likely due to the difficulty in designing molecules that can bind tightly to the ATP-binding site of STK3. Using the 2-(2-amino-5-phenylpyrimidin-4-yl)-5-methoxyphenol (APPP) scaffold identified through virtual screening, we discovered a series of novel, potent STK3 inhibitors with half-maximal inhibitory concentration (IC50) values as low as 3.52 nM. This was made possible through an integrated molecular design strategy that combined structure-based de novo design with a predictive 3D-QSAR model to estimate IC50 values and prioritize compounds for synthesis. This approach improved the prioritization of compounds for synthesis by enhancing binding energy discrimination beyond the limitations of scoring functions in de novo design. Strategic derivatization at four defined positions on the APPP core enhanced interactions in the ATP-binding site of STK3, resulting in 18 of the 25 synthesized derivatives exhibiting IC50 values below 100 nM. These findings are particularly significant given the scarcity of known STK3 inhibitors with comparable potency, while also indicating that 3D-QSAR modeling contributed as a complementary triage tool rather than a standalone driver of lead discovery. This advancement stems from the use of quantum-mechanically derived 3D structural alignments and the incorporation of electrostatic potential distributions as quantitative molecular descriptors. Taken together, this study establishes a robust design paradigm for the rapid development of highly potent kinase inhibitors through structure-based computational strategies.
Computational findings support the prioritization of X14 for further experimental validation in glioblastoma therapy, and generally favorable ADMET profiles were observed, hepatotoxicity alerts were predicted for all compounds, which represents an important limitation supporting the prioritization of X14.
Youssef Briach, M. Er-rajy, Jamal Elkhabchi et al.· Biointerface Research in App...· 0 citations
The results suggest that the scaffold 1,3,4-thiadiazole is a promising structural template for designing new generation aldose reductase inhibitors for diabetic complications.
Priya Devi, Debarshi Mondal, Shalini Sharma et al.· Journal of Pharmaceutical Te...· 0 citations
Pharmacophore analysis, 3D-QSAR, molecular docking, molecular docking, optimization of R-groups, and ADMET studies indicated that the 1,3,4-thiadiazole scaffold could be a promising template for designing potent α-glucosidase inhibitors.
Debarshi Mondal, Priya Devi, Shalini Sharma et al.· Journal of Pharmaceutical Te...· 0 citations
INTRODUCTION/OBJECTIVE
Janus kinase 1 (JAK1) is a key controller and regulator of cytokinemediated immune responses and an effective therapeutic target in autoimmune and inflammatory diseases. In the present study, an in silico workflow was implemented to identify secondary metabolites of mushrooms as prospective JAK1-...
Bushra Shakoor, Ali Irfan, M. T. Muhammed et al.· Current Medicinal Chemistry· 0 citations
The PI3K plays a crucial role in cancer progression, and the development of PI3K inhibitors has always been a hot research direction in oncology. Through virtual screening and docking, potential lead compounds were identified. ADMET prediction revealed that KTC101 possesses superior pharmacokinetic profile. Molecular d...