BDBM50207852 3-isopropyl-N-(4-methyl-3-(3-(4-(methylamino)-1,3,5-triazin-2-yl)pyridin-2-yloxy)phenyl)benzamide::CHEMBL245746

SMILES: CNc1ncnc(n1)-c1cccnc1Oc1cc(NC(=O)c2cccc(c2)C(C)C)ccc1C

InChI Key: InChIKey=OPXHUNQHIWEERC-UHFFFAOYSA-N

Data: 3 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 3 hits for monomerid = 50207852   

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
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50207852 (3-isopropyl-N-(4-methyl-3-(3-(4-(methylamino)-1,3,...) Show SMILES CNc1ncnc(n1)-c1cccnc1Oc1cc(NC(=O)c2cccc(c2)C(C)C)ccc1C Show InChI InChI=1S/C26H26N6O2/c1-16(2)18-7-5-8-19(13-18)24(33)31-20-11-10-17(3)22(14-20)34-25-21(9-6-12-28-25)23-29-15-30-26(27-4)32-23/h5-16H,1-4H3,(H,31,33)(H,27,29,30,32)	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	5	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of Tie2 autophosphorylation in EA.hy926 cells after 2.5 hrs				Bioorg Med Chem Lett 17: 2886-9 (2007) Article DOI: 10.1016/j.bmcl.2007.02.067 BindingDB Entry DOI: 10.7270/Q2445M4C
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50207852 (3-isopropyl-N-(4-methyl-3-(3-(4-(methylamino)-1,3,...) Show SMILES CNc1ncnc(n1)-c1cccnc1Oc1cc(NC(=O)c2cccc(c2)C(C)C)ccc1C Show InChI InChI=1S/C26H26N6O2/c1-16(2)18-7-5-8-19(13-18)24(33)31-20-11-10-17(3)22(14-20)34-25-21(9-6-12-28-25)23-29-15-30-26(27-4)32-23/h5-16H,1-4H3,(H,31,33)(H,27,29,30,32)	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	1	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of Tie2 after 90 mins by HTRF assay				Bioorg Med Chem Lett 17: 2886-9 (2007) Article DOI: 10.1016/j.bmcl.2007.02.067 BindingDB Entry DOI: 10.7270/Q2445M4C
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50207852 (3-isopropyl-N-(4-methyl-3-(3-(4-(methylamino)-1,3,...) Show SMILES CNc1ncnc(n1)-c1cccnc1Oc1cc(NC(=O)c2cccc(c2)C(C)C)ccc1C Show InChI InChI=1S/C26H26N6O2/c1-16(2)18-7-5-8-19(13-18)24(33)31-20-11-10-17(3)22(14-20)34-25-21(9-6-12-28-25)23-29-15-30-26(27-4)32-23/h5-16H,1-4H3,(H,31,33)(H,27,29,30,32)	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	117	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of KDR after 90 mins by HTRF assay				Bioorg Med Chem Lett 17: 2886-9 (2007) Article DOI: 10.1016/j.bmcl.2007.02.067 BindingDB Entry DOI: 10.7270/Q2445M4C
					More data for this Ligand-Target Pair