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BDBM50383672 CHEMBL2030071

SMILES: O=C(N1Cc2ccccc2CC1COc1ccc(cc1)-c1ccccc1)c1cccc2ccccc12

InChI Key: InChIKey=CYSLSCMFHLDXCT-UHFFFAOYSA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50383672   
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
Nuclear receptor subfamily 1 group D member 1


(Homo sapiens)
BDBM50383672
PNG
(CHEMBL2030071)
Show SMILES O=C(N1Cc2ccccc2CC1COc1ccc(cc1)-c1ccccc1)c1cccc2ccccc12
Show InChI InChI=1S/C33H27NO2/c35-33(32-16-8-14-26-11-6-7-15-31(26)32)34-22-28-13-5-4-12-27(28)21-29(34)23-36-30-19-17-25(18-20-30)24-9-2-1-3-10-24/h1-20,29H,21-23H2
PDB
MMDB

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Similars

Article
PubMed
n/an/an/an/a 650n/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Agonist activity at Rev-erbalpha assessed as repression of transcription by luciferase-reporter gene assay


Bioorg Med Chem Lett 22: 3739-42 (2012)

More data for this
Ligand-Target Pair