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SMILES: Oc1ccc(cc1)C(=O)OC(c1ccccc1)c1ccccc1

InChI Key: InChIKey=FQEGPIYLDRANCK-UHFFFAOYSA-N

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 4 hits for monomerid = 50389952   
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
Estrogen receptor


(Homo sapiens (Human))
BDBM50389952
PNG
(CHEMBL2071180)
Show SMILES Oc1ccc(cc1)C(=O)OC(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C20H16O3/c21-18-13-11-17(12-14-18)20(22)23-19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-14,19,21H
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2.55E+3n/an/an/an/an/an/a



East China University of Science and Technology

Curated by ChEMBL


Assay Description
Transcriptional repression of ERalpha receptor expressed in CHO-K1 cells after 24 hrs by luciferase reporter gene assay


Eur J Med Chem 54: 188-96 (2012)


Article DOI: 10.1016/j.ejmech.2012.04.041
BindingDB Entry DOI: 10.7270/Q2445NJ5
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50389952
PNG
(CHEMBL2071180)
Show SMILES Oc1ccc(cc1)C(=O)OC(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C20H16O3/c21-18-13-11-17(12-14-18)20(22)23-19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-14,19,21H
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 290n/an/an/an/an/an/a



East China University of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha receptor LBD expressed in yeast AH109 cells assessed as inhibition of interaction with SRC1 after 24 hrs by alpha-gala...


Eur J Med Chem 54: 188-96 (2012)


Article DOI: 10.1016/j.ejmech.2012.04.041
BindingDB Entry DOI: 10.7270/Q2445NJ5
More data for this
Ligand-Target Pair
Estrogen receptor beta


(Homo sapiens (Human))
BDBM50389952
PNG
(CHEMBL2071180)
Show SMILES Oc1ccc(cc1)C(=O)OC(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C20H16O3/c21-18-13-11-17(12-14-18)20(22)23-19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-14,19,21H
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 180n/an/an/an/an/an/a



East China University of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at ERbeta receptor LBD expressed in yeast AH109 cells assessed as inhibition of interaction with SRC1 after 24 hrs by alpha-galac...


Eur J Med Chem 54: 188-96 (2012)


Article DOI: 10.1016/j.ejmech.2012.04.041
BindingDB Entry DOI: 10.7270/Q2445NJ5
More data for this
Ligand-Target Pair
Estrogen receptor beta


(Homo sapiens (Human))
BDBM50389952
PNG
(CHEMBL2071180)
Show SMILES Oc1ccc(cc1)C(=O)OC(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C20H16O3/c21-18-13-11-17(12-14-18)20(22)23-19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-14,19,21H
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 800n/an/an/an/an/an/a



East China University of Science and Technology

Curated by ChEMBL


Assay Description
Transcriptional repression of ERbeta receptor expressed in CHO-K1 cells after 24 hrs by luciferase reporter gene assay


Eur J Med Chem 54: 188-96 (2012)


Article DOI: 10.1016/j.ejmech.2012.04.041
BindingDB Entry DOI: 10.7270/Q2445NJ5
More data for this
Ligand-Target Pair