BDBM50095411 5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiophene-2-carboxylic acid methyl ester::CHEMBL279560::methyl 5-tert-butyl-3-(3-(4-hydroxyphenyl)ureido)thiophene-2-carboxylate

SMILES: COC(=O)c1sc(cc1NC(=O)Nc1ccc(O)cc1)C(C)(C)C

InChI Key: InChIKey=BAXKULRSDFFZQS-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50095411   

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
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50095411 (5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiop...) Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccc(O)cc1)C(C)(C)C Show InChI InChI=1S/C17H20N2O4S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)19-16(22)18-10-5-7-11(20)8-6-10/h5-9,20H,1-4H3,(H2,18,19,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	610	n/a	n/a	n/a	n/a	n/a	n/a
Bayer Research Center Curated by ChEMBL					Assay Description In vitro inhibition of mitogen-activated protein kinase p38 alpha 2 derived from E. coli				Bioorg Med Chem Lett 11: 9-12 (2001) BindingDB Entry DOI: 10.7270/Q2JM28WH
					More data for this Ligand-Target Pair
RAF proto-oncogene serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50095411 (5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiop...) Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccc(O)cc1)C(C)(C)C Show InChI InChI=1S/C17H20N2O4S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)19-16(22)18-10-5-7-11(20)8-6-10/h5-9,20H,1-4H3,(H2,18,19,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of Raf1 kinase				Bioorg Med Chem Lett 18: 2346-50 (2008) Article DOI: 10.1016/j.bmcl.2008.02.068 BindingDB Entry DOI: 10.7270/Q25X29S8
					More data for this Ligand-Target Pair
RAF proto-oncogene serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50095411 (5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiop...) Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccc(O)cc1)C(C)(C)C Show InChI InChI=1S/C17H20N2O4S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)19-16(22)18-10-5-7-11(20)8-6-10/h5-9,20H,1-4H3,(H2,18,19,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bayer Research Center Curated by ChEMBL					Assay Description Inhibitory concentration against raf kinase.				Bioorg Med Chem Lett 11: 2775-8 (2001) BindingDB Entry DOI: 10.7270/Q2NS0VD5
					More data for this Ligand-Target Pair
RAF proto-oncogene serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50095411 (5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiop...) Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccc(O)cc1)C(C)(C)C Show InChI InChI=1S/C17H20N2O4S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)19-16(22)18-10-5-7-11(20)8-6-10/h5-9,20H,1-4H3,(H2,18,19,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of B-Raf1 (unknown origin)				Eur J Med Chem 44: 1240-9 (2009) Article DOI: 10.1016/j.ejmech.2008.09.016 BindingDB Entry DOI: 10.7270/Q28G8KJ5
					More data for this Ligand-Target Pair