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4I9Z

Crystal structure of the PDE5A1 catalytic domain in complex with novel inhibitors

Summary for 4I9Z
Entry DOI10.2210/pdb4i9z/pdb
Related4IA0
DescriptorcGMP-specific 3',5'-cyclic phosphodiesterase, 5-bromo-2-{5-[(4-methylpiperazin-1-yl)acetyl]-2-propoxyphenyl}-6-(propan-2-yl)pyrimidin-4(3H)-one, ZINC ION, ... (6 entities in total)
Functional Keywordshydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight40884.46
Authors
Ren, J.,Chen, T.,Xu, Y. (deposition date: 2012-12-05, release date: 2014-01-01, Last modification date: 2023-11-08)
Primary citationGong, X.,Wang, G.,Ren, J.,Liu, Z.,Wang, Z.,Chen, T.,Yang, X.,Jiang, X.,Shen, J.,Jiang, H.,Aisa, H.A.,Xu, Y.,Li, J.
Exploration of the 5-bromopyrimidin-4(3H)-ones as potent inhibitors of PDE5.
Bioorg.Med.Chem.Lett., 23:4944-4947, 2013
Cited by
PubMed: 23867165
DOI: 10.1016/j.bmcl.2013.06.062
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.08 Å)
Structure validation

221051

数据于2024-06-12公开中

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