Reaction Details | |||
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Target | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A | ||
Ligand | BDBM50444038 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | In Vitro Assay PDE10A | ||
pH | 7.8±n/a | ||
Temperature | 298.15±n/a K | ||
IC50 | 14±n/a nM | ||
Comments | extracted | ||
Citation | Megens, AA; Langlois, XJ; Andrés-Gil, JI Combinations comprising PDE 2 inhibitors such as 1-aryl-4-methyl-[1,2,4]triazolo-[4,3-A]]quinoxaline compounds and PDE 10 inhibitors for use in the treatment of neurological of metabolic disorders US Patent US9669035 Publication Date 6/6/2017 | ||
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: | PDE10_RAT | Pde10a | Phosphodiesterase 10 | Phosphodiesterase 10A (PDE10A2) | Phosphodiesterase Type 10 (PDE10A) | Rat recombinant PDE10a (rPDE10a) | ||
Type: | Enzyme | ||
Mol. Mass.: | 90160.88 | ||
Organism: | Rattus norvegicus (rat) | ||
Description: | PDE10A was generated from the full-length recombinant rat clone transfected into Sf9 cells. | ||
Residue: | 794 | ||
Sequence: |
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BDBM50444038 | |||
n/a | |||
Name | BDBM50444038 | ||
Synonyms: | CHEMBL3092563 | US9669035, B-5 | ||
Type | Small organic molecule | ||
Emp. Form. | C21H19ClFN5O | ||
Mol. Mass. | 411.86 | ||
SMILES | Cc1nc2ccc(CN3CCOCC3)cc2n2c(nnc12)-c1c(F)cccc1Cl |(32.38,-11.31,;31.04,-12.08,;29.71,-11.31,;28.38,-12.08,;27.05,-11.3,;25.72,-12.08,;25.72,-13.62,;24.39,-14.39,;23.06,-13.63,;23.06,-12.09,;21.73,-11.32,;20.39,-12.09,;20.39,-13.63,;21.73,-14.4,;27.05,-14.38,;28.38,-13.62,;29.71,-14.39,;30.03,-15.9,;31.56,-16.06,;32.19,-14.65,;31.04,-13.62,;28.92,-16.96,;27.44,-16.51,;27.08,-15.02,;26.32,-17.57,;26.68,-19.07,;28.16,-19.51,;29.28,-18.45,;30.75,-18.88,)| | ||
Structure |