Reaction Details | |||
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Target | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A | ||
Ligand | BDBM144648 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | IMAP TR-FRET Assay | ||
Temperature | 298.15±n/a K | ||
IC50 | 15.82±n/a nM | ||
Comments | extracted | ||
Citation | Allen, JR; Frohn, MJ; Harrington, PE; Hu, E; Pickrell, AJ; Rzasa, RM; Sham, KK Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors US Patent US8952037 Publication Date 2/10/2015 | ||
More Info.: | Get all data from this article, Assay Method | ||
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A | |||
Name: | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A | ||
Synonyms: | 3',5'-cyclic phosphodiesterase | 3.1.4.17 | PDE10A | PDE10_HUMAN | Phosphodiesterase 10 (PDE10) | Phosphodiesterase 10A | ||
Type: | Protein | ||
Mol. Mass.: | 88412.52 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q9Y233 | ||
Residue: | 1055 | ||
Sequence: |
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BDBM144648 | |||
n/a | |||
Name | BDBM144648 | ||
Synonyms: | US8952037, 15 | ||
Type | Small organic molecule | ||
Emp. Form. | C24H27N5O2 | ||
Mol. Mass. | 417.5035 | ||
SMILES | CC(=O)N1CCC(CC1)c1nccnc1O[C@H]1C[C@@H](C1)Nc1ccc2ccccc2n1 |r,wU:18.22,wD:16.17,(-4.94,5,;-6.28,4.23,;-7.61,5,;-6.28,2.69,;-4.94,1.93,;-4.94,.38,;-6.28,-.38,;-7.61,.38,;-7.61,1.93,;-6.28,-1.93,;-7.61,-2.69,;-7.61,-4.23,;-6.28,-5,;-4.94,-4.23,;-4.94,-2.69,;-3.61,-1.93,;-2.28,-2.69,;-1.88,-4.18,;-.39,-3.78,;-.79,-2.3,;.94,-4.55,;2.28,-3.78,;2.28,-2.24,;3.61,-1.47,;4.94,-2.24,;6.28,-1.47,;7.61,-2.24,;7.61,-3.78,;6.28,-4.55,;4.94,-3.78,;3.61,-4.55,)| | ||
Structure |