BDBM50488496 CHEMBL2286722

SMILES: Cc1cccc(C(=O)NN(C(=O)c2ccccc2Cl)C(C)(C)C)c1C

InChI Key: InChIKey=JTHVQDOREUEMBU-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 = 50488496   

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)	BDBM50488496 (CHEMBL2286722) Show SMILES Cc1cccc(C(=O)NN(C(=O)c2ccccc2Cl)C(C)(C)C)c1C Show InChI InChI=1S/C20H23ClN2O2/c1-13-9-8-11-15(14(13)2)18(24)22-23(20(3,4)5)19(25)16-10-6-7-12-17(16)21/h6-12H,1-5H3,(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	20	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)	BDBM50488496 (CHEMBL2286722) Show SMILES Cc1cccc(C(=O)NN(C(=O)c2ccccc2Cl)C(C)(C)C)c1C Show InChI InChI=1S/C20H23ClN2O2/c1-13-9-8-11-15(14(13)2)18(24)22-23(20(3,4)5)19(25)16-10-6-7-12-17(16)21/h6-12H,1-5H3,(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	1.15E+4	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