Summary for 11LH
| Entry DOI | 10.2210/pdb11lh/pdb |
| Descriptor | Protein O-GlcNAcase, N~4~-butyl-N~2~-(2,6-dichlorophenyl)pyridine-2,4-diamine (3 entities in total) |
| Functional Keywords | glycoside hydrolase, inhibitor, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor |
| Biological source | Oceanicola granulosus HTCC2516 |
| Total number of polymer chains | 1 |
| Total formula weight | 50552.94 |
| Authors | |
| Primary citation | Bouton, J.,Bretteville, A.,Tresadern, G.,Shaffer, P.,Austin, N.,Buijnsters, P.,Cedervall, E.P.,Darville, N.,Fonteyn, I.,Leenaerts, J.,Lamenca, C.M.,Mertens, L.,Peeters, D.,Velter, A.I.,Roosbroeck, Y.V.,Ebneth, A.,Bartolome, J.M.,Trabanco, A.A.,Oehlrich, D. Discovery of 5‐Azaindole Inhibitors of O‐GlcNAcase for the Treatment of Alzheimer's Disease and Related Tauopathies. Acs Med.Chem.Lett., 17:1096-1105, 2026 Cited by PubMed Abstract: Alzheimer's disease (AD) is a neurodegenerative disorder characterized by extracellular amyloid-β plaque accumulation and intracellular tau neurofibrillary tangles, with tau pathology correlating more closely with cognitive decline. Modulation of tau phosphorylation through the regulation of O-GlcNAcylation, a post-translational modification controlled by O-GlcNAcase (OGA), represents a promising therapeutic strategy. In this study, we report the optimization of a pyrimidine hit identified by high-throughput screening, leading to the discovery and optimization of a novel series of 5-azaindole-based OGA inhibitors. From this series, compound was identified as an tool candidate that demonstrated a favorable pharmacokinetic profile and measurable brain exposure. Pharmacodynamic studies in murine models demonstrated that compound induced a significant and transient elevation of brain O-GlcNAcylation levels, confirming the target engagement. These findings underscore the potential of 5-azaindole-based OGA inhibitors as a novel validated chemotype for modulation of O-GlcNAcylation. PubMed: 42157845DOI: 10.1021/acsmedchemlett.6c00017 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.44 Å) |
Structure validation
Download full validation report






