2026-10-30T00:49:21Zhttps://bayburt-rdlopen.rawdatalibrary.net/oai/request

oai:bayburt-rdlopen.rawdatalibrary.net:bayburt/114972026-10-29T19:41:40Zopenairecom_bayburt_10000col_bayburt_10001com_bayburt_10007col_bayburt_10227

Structure-guided discovery of submicromolar 1,2,4-triazole–Schiff-base inhibitors of glutathione reductaseManap, SevdaAkar, HandeMedetalibeyoğlu, HilalAtalay, AbdurrahmanCan, ZehraKara, YakupAlkan, MuzafferBeytur, MuratYüksek, HaydarOrtaakarsu, Ahmet Buğra1,2,4-triazole–Schiff baseAntioxidant assaysBoltz-2Ferroptosis sensitizationGlutathione reductaseMolecular dynamics simulationsGlutathione reductase (GR) plays a crucial role in maintaining cellular redox balance and is a promising target for ferroptosis-based cancer therapies. In this study, we report the design, synthesis, and comprehensive evaluation of a novel series of 1,2,4-triazole–Schiff base succinate derivatives (AUR-514–518) as potent GR inhibitors. In vitro Mannervik assays revealed vigorous submicromolar inhibitory activity, with AUR-517 emerging as the most effective (IC50 = 0.471 ± 0.032 μM), significantly surpassing quercetin (IC50 = 214.5 ± 18.5 μM). Antioxidant profiling revealed negligible radical scavenging activity; however, modest CUPRAC responses suggest a target-specific mechanism. To elucidate the molecular determinants of inhibition, we employed deep-learning–assisted protein–ligand affinity predictions, molecular dynamics simulations, MM/GBSA free-energy calculations, and dimensional reduction analyses. These computational studies revealed dual binding modes at both the catalytic site and dimer interface, with AUR-517 forming stable interactions with key catalytic residues, consistent with experimental potency rankings. The RMSD/RMSF profiles indicated enhanced conformational stability of GR–ligand complexes, while binding energy landscapes underscored the superior stability of AUR-517. Consequently, these findings establish the AUR series as a new class of structurally validated GR inhibitors, with AUR-517 representing a lead scaffold for the rational development of ferroptosis-sensitizing agents with translational potential in oncology.Elsevier B.V.2026Articlehttps://rdlopen.rawdatalibrary.net/r/bayburt/11497https://doi.org/10.1016/j.ijbiomac.2025.1494710141-8130enInternational Journal of Biological Macromoleculesinfo:eu-repo/semantics/closedAccessinfo:eu-repo/semantics/articlehttps://bayburt-rdlopen.rawdatalibrary.net/tr/items/bayburt/11497