9WP3
The crystal structure of PDE2A complexed with inhibitor 13j
This is a non-PDB format compatible entry.
Summary for 9WP3
| Entry DOI | 10.2210/pdb9wp3/pdb |
| Descriptor | cGMP-dependent 3',5'-cyclic phosphodiesterase, ZINC ION, MAGNESIUM ION, ... (5 entities in total) |
| Functional Keywords | pde2a inhibitor, hydrolase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 4 |
| Total formula weight | 160878.66 |
| Authors | |
| Primary citation | Yang, F.,Guo, Q.,Chen, M.,Wang, W.,Chen, X.,Zhang, S.,Bian, H.,Li, J.,Jiao, Z.,Wang, Q.,Xiong, W.,Huang, Y.Y.,Liu, Y.,Xu, C.,Huang, L. Discovery of novel 2,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one derivatives as PDE2 inhibitors with Alzheimer's disease therapeutic potential. Eur.J.Med.Chem., 302:118302-118302, 2026 Cited by PubMed Abstract: Phosphodiesterase 2 (PDE2), a dual-substrate cyclic nucleotide hydrolase, represents a potential therapeutic target for cognitive impairment. This study aims to develop 2,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one-based PDE2 inhibitors with favorable drug-like properties for the treatment of Alzheimer's disease. Through scaffold hopping and cocrystal structure analysis, compound 14c was identified as an effective PDE2 inhibitor (IC = 0.6 μM, aqueous solubility = 60.36 μg/mL). Moreover, 14c demonstrated favorable hepatic microsomal stability, pharmacokinetic properties (t = 4.4 h, F% = 95.66 %) and promising safety both in vitro and in vivo. In the OKA-induced AD mice models, administration of 14c significantly improved memory deficits and cognitive impairment. Molecular mechanism studies revealed that the neuroprotective effects of 14c were mediated through the PKA/CREB/BDNF signaling pathway. Collectively, these findings represent significant advances in developing PDE2 inhibitors with favorable drug-like properties and establish a solid foundation for their therapeutic application in AD. PubMed: 41151129DOI: 10.1016/j.ejmech.2025.118302 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.50183917707 Å) |
Structure validation
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