BDBM50207502 1-(4-(3-amino-1H-indazol-4-yl)phenyl)-3-(3-hydroxyphenyl)urea::CHEMBL223304::N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(3-hydroxyphenyl)urea

SMILES: Nc1n[nH]c2cccc(-c3ccc(NC(=O)Nc4cccc(O)c4)cc3)c12

InChI Key: InChIKey=OPTYQCYBVIBKCC-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 = 50207502   

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
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50207502 (1-(4-(3-amino-1H-indazol-4-yl)phenyl)-3-(3-hydroxy...) Show SMILES Nc1n[nH]c2cccc(-c3ccc(NC(=O)Nc4cccc(O)c4)cc3)c12 Show InChI InChI=1S/C20H17N5O2/c21-19-18-16(5-2-6-17(18)24-25-19)12-7-9-13(10-8-12)22-20(27)23-14-3-1-4-15(26)11-14/h1-11,26H,(H3,21,24,25)(H2,22,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	55	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of VEGF-induced human KDR phosphorylation in mouse 3T3 cells by ELISA				J Med Chem 50: 1584-97 (2007) Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95
					More data for this Ligand-Target Pair
Mast/stem cell growth factor receptor Kit (Homo sapiens (Human))	BDBM50207502 (1-(4-(3-amino-1H-indazol-4-yl)phenyl)-3-(3-hydroxy...) Show SMILES Nc1n[nH]c2cccc(-c3ccc(NC(=O)Nc4cccc(O)c4)cc3)c12 Show InChI InChI=1S/C20H17N5O2/c21-19-18-16(5-2-6-17(18)24-25-19)12-7-9-13(10-8-12)22-20(27)23-14-3-1-4-15(26)11-14/h1-11,26H,(H3,21,24,25)(H2,22,23,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
Punjabi University Curated by ChEMBL					Assay Description Inhibition of c-Kit by HTRF method				Eur J Med Chem 45: 393-404 (2010) Article DOI: 10.1016/j.ejmech.2009.09.013 BindingDB Entry DOI: 10.7270/Q2RX9C6D
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human))	BDBM50207502 (1-(4-(3-amino-1H-indazol-4-yl)phenyl)-3-(3-hydroxy...) Show SMILES Nc1n[nH]c2cccc(-c3ccc(NC(=O)Nc4cccc(O)c4)cc3)c12 Show InChI InChI=1S/C20H17N5O2/c21-19-18-16(5-2-6-17(18)24-25-19)12-7-9-13(10-8-12)22-20(27)23-14-3-1-4-15(26)11-14/h1-11,26H,(H3,21,24,25)(H2,22,23,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of FLT3 by HTRF assay				J Med Chem 50: 1584-97 (2007) Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95
					More data for this Ligand-Target Pair
Mast/stem cell growth factor receptor Kit (Homo sapiens (Human))	BDBM50207502 (1-(4-(3-amino-1H-indazol-4-yl)phenyl)-3-(3-hydroxy...) Show SMILES Nc1n[nH]c2cccc(-c3ccc(NC(=O)Nc4cccc(O)c4)cc3)c12 Show InChI InChI=1S/C20H17N5O2/c21-19-18-16(5-2-6-17(18)24-25-19)12-7-9-13(10-8-12)22-20(27)23-14-3-1-4-15(26)11-14/h1-11,26H,(H3,21,24,25)(H2,22,23,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of c-Kit by HTRF assay				J Med Chem 50: 1584-97 (2007) Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95
					More data for this Ligand-Target Pair