BDBM50418300 CHEMBL1765941

SMILES: CCCCCCC1=C(c2ccccc2)[C@@]2(CCC[C@@H]2C1)C(=C)CCC

InChI Key: InChIKey=YRRVMTFIZZROJG-NOZRDPDXSA-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 = 50418300   

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
Steroidogenic Factor 1 (Homo sapiens (Human))	BDBM50418300 (CHEMBL1765941) Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CCC[C@@H]2C1)C(=C)CCC |r,c:6| Show InChI InChI=1S/C25H36/c1-4-6-7-9-16-22-19-23-17-12-18-25(23,20(3)13-5-2)24(22)21-14-10-8-11-15-21/h8,10-11,14-15,23H,3-7,9,12-13,16-19H2,1-2H3/t23-,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	158	n/a	n/a	n/a	n/a
University of Southampton Curated by ChEMBL					Assay Description Agonist activity at human SF-1 assessed as DAX1 1-23 peptide recruitment by TR-FRET assay relative to control				J Med Chem 54: 2266-81 (2011) Article DOI: 10.1021/jm1014296 BindingDB Entry DOI: 10.7270/Q29Z957P
					More data for this Ligand-Target Pair
Liver Receptor Homolog 1 (Homo sapiens (Human))	BDBM50418300 (CHEMBL1765941) Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CCC[C@@H]2C1)C(=C)CCC |r,c:6| Show InChI InChI=1S/C25H36/c1-4-6-7-9-16-22-19-23-17-12-18-25(23,20(3)13-5-2)24(22)21-14-10-8-11-15-21/h8,10-11,14-15,23H,3-7,9,12-13,16-19H2,1-2H3/t23-,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a
University of Southampton Curated by ChEMBL					Assay Description Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to control				J Med Chem 54: 2266-81 (2011) Article DOI: 10.1021/jm1014296 BindingDB Entry DOI: 10.7270/Q29Z957P
					More data for this Ligand-Target Pair