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Updated: Jan 16, 2026

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
Published on: May 9, 2025
Design, synthesis, biological activity and molecular docking studies of triazolopyridine derivatives as ASK1
Sheng Su1, Mengyao Peng1, Xiaorui Han1
1College of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang 330004, PR China.
Abstract:
Apoptosis signal-regulating kinase 1 (ASK1, MAP3K5) is a pivotal mediator in the MAPK pathway, regulating inflammation and fibrosis in Non-alcoholic Steatohepatitis (NASH). A series of novel triazolopyridine derivatives were designed and synthesized as ASK1 inhibitors. Systematic SAR studies identified compound 16a as a potent inhibitor (IC50 = 149.1 nM). Significantly, 16a reduced lipid accumulation in LO2 cells, evidenced by decreased Oil Red O-stained lipid droplets and lowered LDL-C, T-CHO, and TG levels in NASH model cells. Mechanistic studies revealed that 16a suppressed TNF-α-induced activation of the ASK1-p38/JNK signaling pathway in HGC-27 cells and modulated apoptosis-related proteins. These findings highlight 16a as a promising candidate for anti-NASH therapy.
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