Reaction Details |
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Target | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A [440-779] |
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Ligand | BDBM164283 |
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Substrate/Competitor | n/a |
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Meas. Tech. | PDE10A Inhibition Assay |
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Temperature | 298.15±n/a K |
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IC50 | 0.54±n/a nM |
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Comments | extracted |
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Citation | Püschl, A; Nielsen, J; Kehler, J; Kilburn, JP; Marigo, M; Langgård, M Heteroaromatic phenylimidazole derivatives as PDE10A enzyme inhibitors US Patent US9669029 Publication Date 6/6/2017 |
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More Info.: | Get all data from this article, Assay Method |
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cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A [440-779] |
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Name: | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A [440-779] |
Synonyms: | PDE10A | PDE10_HUMAN | PED10A | Phosphodiesterase 10A (PDE10A) |
Type: | n/a |
Mol. Mass.: | 39060.01 |
Organism: | Homo sapiens (Human) |
Description: | Q9Y233[440-779] |
Residue: | 340 |
Sequence: | ICTSEEWQGLMQFTLPVRLCKEIELFHFDIGPFENMWPGIFVYMVHRSCGTSCFELEKLC
RFIMSVKKNYRRVPYHNWKHAVTVAHCMYAILQNNHTLFTDLERKGLLIACLCHDLDHRG
FSNSYLQKFDHPLAALYSTSTMEQHHFSQTVSILQLEGHNIFSTLSSSEYEQVLEIIRKA
IIATDLALYFGNRKQLEEMYQTGSLNLNNQSHRDRVIGLMMTACDLCSVTKLWPVTKLTA
NDIYAEFWAEGDEMKKLGIQPIPMMDRDKKDEVPQGQLGFYNAVAIPCYTTLTQILPPTE
PLLKACRDNLSQWEKVIRGEETATWISSPSVAQKAAASED
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BDBM164283 |
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n/a |
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Name | BDBM164283 |
Synonyms: | US9669029, 33 5-Methyl-2-[2-(4-thiophen-2-yl-1H-imidazol-2-yl)-ethyl]-[1,2,4]triazolo[1,5-a]pyridine |
Type | Small organic molecule |
Emp. Form. | C16H17N5S |
Mol. Mass. | 311.405 |
SMILES | CC1=CC=CC2NC(CCc3nc(c[nH]3)-c3cccs3)=NN12 |c:3,21,t:1| |
Structure |
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