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BDBM50418299 CHEMBL1765926

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

InChI Key: InChIKey=DTLDZNVFJVINHS-IRLDBZIGSA-N

Data: 2 EC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50418299   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Steroidogenic Factor 1


(Homo sapiens (Human))
BDBM50418299
PNG
(CHEMBL1765926)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CCC[C@@H]2C1)OCC |r,c:6|
Show InChI InChI=1S/C22H32O/c1-3-5-6-8-14-19-17-20-15-11-16-22(20,23-4-2)21(19)18-12-9-7-10-13-18/h7,9-10,12-13,20H,3-6,8,11,14-17H2,1-2H3/t20-,22+/m1/s1
PDB
MMDB

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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 501n/an/an/an/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))
BDBM50418299
PNG
(CHEMBL1765926)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CCC[C@@H]2C1)OCC |r,c:6|
Show InChI InChI=1S/C22H32O/c1-3-5-6-8-14-19-17-20-15-11-16-22(20,23-4-2)21(19)18-12-9-7-10-13-18/h7,9-10,12-13,20H,3-6,8,11,14-17H2,1-2H3/t20-,22+/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 2.51E+3n/an/an/an/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