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SMILES: Clc1ccccc1Cn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C#N

InChI Key: InChIKey=PBRDIOBUEFYJEQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 276051   

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
Lysine-specific demethylase 2B (Homo sapiens (Human))	BDBM276051 (4-[2-[1-[(2-chlorophenyl)methyl]imidazol-4-yl]pyri...) Show SMILES Clc1ccccc1Cn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C#N Show InChI InChI=1S/C18H12ClN7/c19-14-4-2-1-3-13(14)9-26-10-17(22-11-26)15-7-12(5-6-21-15)18-16(8-20)23-25-24-18/h1-7,10-11H,9H2,(H,23,24,25)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<100	n/a	n/a	n/a	n/a	n/a	25
Celgene Quanticel Research, Inc. US Patent					Assay Description The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...				US Patent US10071984 (2018) BindingDB Entry DOI: 10.7270/Q24Q7X0X
					More data for this Ligand-Target Pair
Histone lysine demethylase PHF8 (Homo sapiens (Human))	BDBM276051 (4-[2-[1-[(2-chlorophenyl)methyl]imidazol-4-yl]pyri...) Show SMILES Clc1ccccc1Cn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C#N Show InChI InChI=1S/C18H12ClN7/c19-14-4-2-1-3-13(14)9-26-10-17(22-11-26)15-7-12(5-6-21-15)18-16(8-20)23-25-24-18/h1-7,10-11H,9H2,(H,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>500	n/a	n/a	n/a	n/a	n/a	n/a
GSK					Assay Description PHF8 Assay: The ability of test compounds to inhibit the activity of PHF8 was determined in 384-well plate format under the following reaction condit...				Bioorg Med Chem Lett 17: 1584-9 (2007) BindingDB Entry DOI: 10.7270/Q2FT8PBQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 2B (Homo sapiens (Human))	BDBM276051 (4-[2-[1-[(2-chlorophenyl)methyl]imidazol-4-yl]pyri...) Show SMILES Clc1ccccc1Cn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C#N Show InChI InChI=1S/C18H12ClN7/c19-14-4-2-1-3-13(14)9-26-10-17(22-11-26)15-7-12(5-6-21-15)18-16(8-20)23-25-24-18/h1-7,10-11H,9H2,(H,23,24,25)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<100	n/a	n/a	n/a	n/a	n/a	n/a
GSK					Assay Description The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...				Bioorg Med Chem Lett 17: 1584-9 (2007) BindingDB Entry DOI: 10.7270/Q2FT8PBQ
					More data for this Ligand-Target Pair
Isoform 2 of Histone lysine demethylase PHF8 (2) (Homo sapiens (Human))	BDBM276051 (4-[2-[1-[(2-chlorophenyl)methyl]imidazol-4-yl]pyri...) Show SMILES Clc1ccccc1Cn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C#N Show InChI InChI=1S/C18H12ClN7/c19-14-4-2-1-3-13(14)9-26-10-17(22-11-26)15-7-12(5-6-21-15)18-16(8-20)23-25-24-18/h1-7,10-11H,9H2,(H,23,24,25)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	25
Celgene Quanticel Research, Inc. US Patent					Assay Description The ability of test compounds to inhibit the activity of PHF8 was determined in 384-well plate format under the following reaction conditions: 3 nM P...				US Patent US10071984 (2018) BindingDB Entry DOI: 10.7270/Q24Q7X0X
					More data for this Ligand-Target Pair