Reaction Details | |||
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Target | cGMP-specific 3',5'-cyclic phosphodiesterase | ||
Ligand | BDBM50196764 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_1618821 (CHEMBL3860990) | ||
IC50 | 13±n/a nM | ||
Citation | Rabal, O; Sánchez-Arias, JA; Cuadrado-Tejedor, M; de Miguel, I; Pérez-González, M; García-Barroso, C; Ugarte, A; Estella-Hermoso de Mendoza, A; Sáez, E; Espelosin, M; Ursua, S; Haizhong, T; Wei, W; Musheng, X; Garcia-Osta, A; Oyarzabal, J Design, Synthesis, and Biological Evaluation of First-in-Class Dual Acting Histone Deacetylases (HDACs) and Phosphodiesterase 5 (PDE5) Inhibitors for the Treatment of Alzheimer's Disease. J Med Chem59:8967-9004 (2016) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
cGMP-specific 3',5'-cyclic phosphodiesterase | |||
Name: | cGMP-specific 3',5'-cyclic phosphodiesterase | ||
Synonyms: | 3',5'-cyclic phosphodiesterase | CGB-PDE | PDE5 | PDE5A | PDE5A_HUMAN | Phosphodiesterase 2 and 5 (PDE2 and PDE5) | Phosphodiesterase 5 (PDE5) | Phosphodiesterase 5A | Phosphodiesterase 5A (PDE5A) | cGMP-binding cGMP-specific phosphodiesterase | cGMP-specific 3',5'-cyclic phosphodiesterase | ||
Type: | Protein | ||
Mol. Mass.: | 99975.83 | ||
Organism: | Homo sapiens (Human) | ||
Description: | O76074 | ||
Residue: | 875 | ||
Sequence: |
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BDBM50196764 | |||
n/a | |||
Name | BDBM50196764 | ||
Synonyms: | CHEMBL3970271 | ||
Type | Small organic molecule | ||
Emp. Form. | C24H31N5O4 | ||
Mol. Mass. | 453.534 | ||
SMILES | CCOc1ccc(C[C@H]2CC[C@@H](CC2)C(=O)NO)cc1-c1nc2c(CC)nn(C)c2c(=O)[nH]1 |r,wU:8.7,wD:11.14,(2.03,-1.64,;2.03,-3.18,;3.37,-3.95,;3.37,-5.49,;2.04,-6.26,;2.04,-7.81,;3.38,-8.57,;3.39,-10.11,;4.73,-10.88,;6.05,-10.09,;7.38,-10.87,;7.39,-12.41,;6.05,-13.18,;4.72,-12.42,;8.72,-13.18,;8.72,-14.72,;10.05,-12.41,;11.38,-13.18,;4.71,-7.8,;4.7,-6.26,;6.04,-5.49,;7.36,-6.25,;8.69,-5.48,;10.15,-5.96,;10.63,-7.42,;12.13,-7.74,;11.05,-4.72,;10.15,-3.48,;10.63,-2.01,;8.69,-3.95,;7.36,-3.17,;7.36,-1.63,;6.04,-3.95,)| | ||
Structure |