BDBM50304841 4-(2-hydroxyphenyl)-1,2-dimethyl-5-(quinoxalin-6-yl)-1H-pyrazol-3(2H)-one::CHEMBL605302

SMILES: Cn1c(c(-c2ccccc2O)c(=O)n1C)-c1ccc2nccnc2c1

InChI Key: InChIKey=AGBOCXHAVXPLBP-UHFFFAOYSA-N

Data: 1 KI  1 IC50

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 2 hits for monomerid = 50304841   

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
TGF-beta receptor type-1 (Homo sapiens (Human))	BDBM50304841 (4-(2-hydroxyphenyl)-1,2-dimethyl-5-(quinoxalin-6-y...) Show SMILES Cn1c(c(-c2ccccc2O)c(=O)n1C)-c1ccc2nccnc2c1 |(.31,-34.54,;-.32,-33.14,;-1.83,-32.82,;-1.99,-31.29,;-3.33,-30.52,;-4.67,-31.29,;-6,-30.52,;-6,-28.97,;-4.67,-28.2,;-3.34,-28.97,;-2,-28.19,;-.59,-30.66,;-.27,-29.15,;.45,-31.8,;1.98,-31.64,;-3.15,-33.61,;-4.5,-32.86,;-5.82,-33.65,;-5.78,-35.19,;-7.1,-35.98,;-7.07,-37.53,;-5.72,-38.27,;-4.4,-37.48,;-4.43,-35.94,;-3.12,-35.15,)| Show InChI InChI=1S/C19H16N4O2/c1-22-18(12-7-8-14-15(11-12)21-10-9-20-14)17(19(25)23(22)2)13-5-3-4-6-16(13)24/h3-11,24H,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Biogen Idec Inc. Curated by ChEMBL					Assay Description Displacement of [3H]HTS446284 from human recombinant His-tagged TGFbetaR1 after 1 hr by scintillation counting				Bioorg Med Chem Lett 20: 326-9 (2010) Article DOI: 10.1016/j.bmcl.2009.10.108 BindingDB Entry DOI: 10.7270/Q2RN37ZK
					More data for this Ligand-Target Pair
TGF-beta receptor type-1 (Homo sapiens (Human))	BDBM50304841 (4-(2-hydroxyphenyl)-1,2-dimethyl-5-(quinoxalin-6-y...) Show SMILES Cn1c(c(-c2ccccc2O)c(=O)n1C)-c1ccc2nccnc2c1 |(.31,-34.54,;-.32,-33.14,;-1.83,-32.82,;-1.99,-31.29,;-3.33,-30.52,;-4.67,-31.29,;-6,-30.52,;-6,-28.97,;-4.67,-28.2,;-3.34,-28.97,;-2,-28.19,;-.59,-30.66,;-.27,-29.15,;.45,-31.8,;1.98,-31.64,;-3.15,-33.61,;-4.5,-32.86,;-5.82,-33.65,;-5.78,-35.19,;-7.1,-35.98,;-7.07,-37.53,;-5.72,-38.27,;-4.4,-37.48,;-4.43,-35.94,;-3.12,-35.15,)| Show InChI InChI=1S/C19H16N4O2/c1-22-18(12-7-8-14-15(11-12)21-10-9-20-14)17(19(25)23(22)2)13-5-3-4-6-16(13)24/h3-11,24H,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD 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
Biogen Idec Inc. Curated by ChEMBL					Assay Description Inhibition of TGFR-1 in human HepG2 cells expressing PAI-luciferase by luciferase reporter gene assay				Bioorg Med Chem Lett 20: 326-9 (2010) Article DOI: 10.1016/j.bmcl.2009.10.108 BindingDB Entry DOI: 10.7270/Q2RN37ZK
					More data for this Ligand-Target Pair