BDBM147139 US8957077, 1-9

SMILES: Cc1nc(C)c(CNc2cc(nc3ccnn23)C2CC2)s1

InChI Key: InChIKey=QXEIYUPKPSVTRP-UHFFFAOYSA-N

Data: 2 KI  1 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 147139   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A (Homo sapiens (Human))	BDBM147139 (US8957077, 1-9) Show SMILES Cc1nc(C)c(CNc2cc(nc3ccnn23)C2CC2)s1 Show InChI InChI=1S/C15H17N5S/c1-9-13(21-10(2)18-9)8-16-15-7-12(11-3-4-11)19-14-5-6-17-20(14)15/h5-7,11,16H,3-4,8H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	9.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Sharp & Dohme Corp. US Patent					Assay Description In a typical experiment the PDE10 inhibitory activity of the compounds of the present invention was determined in accordance with the following exper...				US Patent US8957077 (2015) BindingDB Entry DOI: 10.7270/Q29G5KHW
					More data for this Ligand-Target Pair
3',5'-cyclic phosphodiesterase (Homo sapiens (Human))	BDBM147139 (US8957077, 1-9) Show SMILES Cc1nc(C)c(CNc2cc(nc3ccnn23)C2CC2)s1 Show InChI InChI=1S/C15H17N5S/c1-9-13(21-10(2)18-9)8-16-15-7-12(11-3-4-11)19-14-5-6-17-20(14)15/h5-7,11,16H,3-4,8H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	9.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of PDE10A (unknown origin) by IMAP assay				Bioorg Med Chem Lett 26: 126-32 (2016) Article DOI: 10.1016/j.bmcl.2015.11.013 BindingDB Entry DOI: 10.7270/Q2NP27FW
					More data for this Ligand-Target Pair
Pregnane X receptor (Homo sapiens (Human))	BDBM147139 (US8957077, 1-9) Show SMILES Cc1nc(C)c(CNc2cc(nc3ccnn23)C2CC2)s1 Show InChI InChI=1S/C15H17N5S/c1-9-13(21-10(2)18-9)8-16-15-7-12(11-3-4-11)19-14-5-6-17-20(14)15/h5-7,11,16H,3-4,8H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>2.50E+5	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Activation of PXR (unknown origin)				Bioorg Med Chem Lett 26: 126-32 (2016) Article DOI: 10.1016/j.bmcl.2015.11.013 BindingDB Entry DOI: 10.7270/Q2NP27FW
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM147139 (US8957077, 1-9) Show SMILES Cc1nc(C)c(CNc2cc(nc3ccnn23)C2CC2)s1 Show InChI InChI=1S/C15H17N5S/c1-9-13(21-10(2)18-9)8-16-15-7-12(11-3-4-11)19-14-5-6-17-20(14)15/h5-7,11,16H,3-4,8H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of CYP3A4 (unknown origin)				Bioorg Med Chem Lett 26: 126-32 (2016) Article DOI: 10.1016/j.bmcl.2015.11.013 BindingDB Entry DOI: 10.7270/Q2NP27FW
					More data for this Ligand-Target Pair