Compile Data Set for Download or QSAR

Found 4 hits of ic50 for monomerid = 50045597   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
P2Y purinoceptor 1 (Homo sapiens (Human))	BDBM50045597 (CHEMBL3314321 | US9428504, 152) Show SMILES CC(C)(C)CN1CCC2(CN(c3c2c(c(F)cc3O)-c2ccc(F)cc2)c2ccccc2NC(=O)Nc2nc3ccc(Cl)nc3s2)CC1 Show InChI InChI=1S/C36H35ClF2N6O2S/c1-35(2,3)19-44-16-14-36(15-17-44)20-45(31-27(46)18-23(39)29(30(31)36)21-8-10-22(38)11-9-21)26-7-5-4-6-24(26)40-33(47)43-34-41-25-12-13-28(37)42-32(25)48-34/h4-13,18,46H,14-17,19-20H2,1-3H3,(H2,40,41,43,47)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.120	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Research Curated by ChEMBL					Assay Description Antagonist activity at P2Y1 receptor in washed human platelets assessed as 1 uM 2-methylthio-ADP-induced calcium flux by FLIPR assay				J Med Chem 57: 6150-64 (2014) Article DOI: 10.1021/jm5006226 BindingDB Entry DOI: 10.7270/Q20Z74XP
					More data for this Ligand-Target Pair
P2Y purinoceptor 1 (Homo sapiens (Human))	BDBM50045597 (CHEMBL3314321 | US9428504, 152) Show SMILES CC(C)(C)CN1CCC2(CN(c3c2c(c(F)cc3O)-c2ccc(F)cc2)c2ccccc2NC(=O)Nc2nc3ccc(Cl)nc3s2)CC1 Show InChI InChI=1S/C36H35ClF2N6O2S/c1-35(2,3)19-44-16-14-36(15-17-44)20-45(31-27(46)18-23(39)29(30(31)36)21-8-10-22(38)11-9-21)26-7-5-4-6-24(26)40-33(47)43-34-41-25-12-13-28(37)42-32(25)48-34/h4-13,18,46H,14-17,19-20H2,1-3H3,(H2,40,41,43,47)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Research Curated by ChEMBL					Assay Description Antagonist activity at P2Y1 receptor in platelet-enriched human plasma assessed as 10 uM ADP-induced platelet aggregation preincubated for 1 min foll...				J Med Chem 57: 6150-64 (2014) Article DOI: 10.1021/jm5006226 BindingDB Entry DOI: 10.7270/Q20Z74XP
					More data for this Ligand-Target Pair
P2Y purinoceptor 2 (Homo sapiens (Human))	BDBM50045597 (CHEMBL3314321 | US9428504, 152) Show SMILES CC(C)(C)CN1CCC2(CN(c3c2c(c(F)cc3O)-c2ccc(F)cc2)c2ccccc2NC(=O)Nc2nc3ccc(Cl)nc3s2)CC1 Show InChI InChI=1S/C36H35ClF2N6O2S/c1-35(2,3)19-44-16-14-36(15-17-44)20-45(31-27(46)18-23(39)29(30(31)36)21-8-10-22(38)11-9-21)26-7-5-4-6-24(26)40-33(47)43-34-41-25-12-13-28(37)42-32(25)48-34/h4-13,18,46H,14-17,19-20H2,1-3H3,(H2,40,41,43,47)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Research Curated by ChEMBL					Assay Description Antagonist activity at P2Y2 receptor (unknown origin)				J Med Chem 57: 6150-64 (2014) Article DOI: 10.1021/jm5006226 BindingDB Entry DOI: 10.7270/Q20Z74XP
					More data for this Ligand-Target Pair
P2Y purinoceptor 12 (Homo sapiens (Human))	BDBM50045597 (CHEMBL3314321 | US9428504, 152) Show SMILES CC(C)(C)CN1CCC2(CN(c3c2c(c(F)cc3O)-c2ccc(F)cc2)c2ccccc2NC(=O)Nc2nc3ccc(Cl)nc3s2)CC1 Show InChI InChI=1S/C36H35ClF2N6O2S/c1-35(2,3)19-44-16-14-36(15-17-44)20-45(31-27(46)18-23(39)29(30(31)36)21-8-10-22(38)11-9-21)26-7-5-4-6-24(26)40-33(47)43-34-41-25-12-13-28(37)42-32(25)48-34/h4-13,18,46H,14-17,19-20H2,1-3H3,(H2,40,41,43,47)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Research Curated by ChEMBL					Assay Description Antagonist activity at P2Y12 receptor (unknown origin)				J Med Chem 57: 6150-64 (2014) Article DOI: 10.1021/jm5006226 BindingDB Entry DOI: 10.7270/Q20Z74XP
					More data for this Ligand-Target Pair