BDBM50488497 CHEMBL2286719

SMILES: Cc1ccc(cc1)C(=O)NN(C(=O)c1ccccc1Cl)C(C)(C)C

InChI Key: InChIKey=CDBUBDOIZDUJLX-UHFFFAOYSA-N

Data: 3 EC50

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 = 50488497   

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
Protein ultraspiracle (Drosophila melanogaster)	BDBM50488497 (CHEMBL2286719) Show SMILES Cc1ccc(cc1)C(=O)NN(C(=O)c1ccccc1Cl)C(C)(C)C Show InChI InChI=1S/C19H21ClN2O2/c1-13-9-11-14(12-10-13)17(23)21-22(19(2,3)4)18(24)15-7-5-6-8-16(15)20/h5-12H,1-4H3,(H,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	3.24E+3	n/a	n/a	n/a	n/a
Ghent University Curated by ChEMBL					Assay Description Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells after 24 hr by luciferase reporter gene assay				Pest Manag Sci 66: 1215-29 (2010) Article DOI: 10.1002/ps.1998 BindingDB Entry DOI: 10.7270/Q2FT8PXB
					More data for this Ligand-Target Pair
Ecdysone receptor (Bombyx mori)	BDBM50488497 (CHEMBL2286719) Show SMILES Cc1ccc(cc1)C(=O)NN(C(=O)c1ccccc1Cl)C(C)(C)C Show InChI InChI=1S/C19H21ClN2O2/c1-13-9-11-14(12-10-13)17(23)21-22(19(2,3)4)18(24)15-7-5-6-8-16(15)20/h5-12H,1-4H3,(H,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	19	n/a	n/a	n/a	n/a
Ghent University Curated by ChEMBL					Assay Description Agonist activity at ecdysone receptor in Bombyx mori Bm5 cells after 24 hr by luciferase reporter gene assay				Pest Manag Sci 66: 1215-29 (2010) Article DOI: 10.1002/ps.1998 BindingDB Entry DOI: 10.7270/Q2FT8PXB
					More data for this Ligand-Target Pair
Protein ultraspiracle (Drosophila melanogaster)	BDBM50488497 (CHEMBL2286719) Show SMILES Cc1ccc(cc1)C(=O)NN(C(=O)c1ccccc1Cl)C(C)(C)C Show InChI InChI=1S/C19H21ClN2O2/c1-13-9-11-14(12-10-13)17(23)21-22(19(2,3)4)18(24)15-7-5-6-8-16(15)20/h5-12H,1-4H3,(H,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	219	n/a	n/a	n/a	n/a
Ghent University Curated by ChEMBL					Assay Description Agonist activity at ecdysone receptor in Drosophila melanogaster B2 cells assessed as reduction in cell density				Pest Manag Sci 66: 1215-29 (2010) Article DOI: 10.1002/ps.1998 BindingDB Entry DOI: 10.7270/Q2FT8PXB
					More data for this Ligand-Target Pair