BDBM50488482 CHEMBL2286721

SMILES: CC(C)(C)N(NC(=O)c1cccc(Cl)c1Cl)C(=O)c1ccccc1Cl

InChI Key: InChIKey=OQJGHOJKYUGBFU-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50488482   

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
Ecdysone receptor (Bombyx mori)	BDBM50488482 (CHEMBL2286721) Show SMILES CC(C)(C)N(NC(=O)c1cccc(Cl)c1Cl)C(=O)c1ccccc1Cl Show InChI InChI=1S/C18H17Cl3N2O2/c1-18(2,3)23(17(25)11-7-4-5-9-13(11)19)22-16(24)12-8-6-10-14(20)15(12)21/h4-10H,1-3H3,(H,22,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	9.30	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
Ecdysone receptor (Drosophila melanogaster)	BDBM50488482 (CHEMBL2286721) Show SMILES CC(C)(C)N(NC(=O)c1cccc(Cl)c1Cl)C(=O)c1ccccc1Cl Show InChI InChI=1S/C18H17Cl3N2O2/c1-18(2,3)23(17(25)11-7-4-5-9-13(11)19)22-16(24)12-8-6-10-14(20)15(12)21/h4-10H,1-3H3,(H,22,24)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	7.76E+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