BDBM50430575 CHEMBL2337794

SMILES CC1=C(CC(O)=O)c2cc(F)ccc2\C1=C/c1ccccc1

InChI Key InChIKey=MVHHIVKPIOEVNA-UHFFFAOYSA-N

Data  1 IC50  1 Kd  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50430575   

TargetPeroxisome proliferator-activated receptor gamma(Human)
Xiamen University

Curated by ChEMBL
LigandPNGBDBM50430575(CHEMBL2337794)
Affinity DataEC50:  2.78E+3nMAssay Description:Partial agonist activity at GAL4 DBD-fused PPARgamma LBD (unknown origin) expressed in pG5 luc and pBIND transfected HEK293T cells assessed as transc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2022
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Xiamen University

Curated by ChEMBL
LigandPNGBDBM50430575(CHEMBL2337794)
Affinity DataKd:  7.94E+3nMAssay Description:Binding affinity to GAL4-DBD-fused PPARgamma ligand binding domain (unknown origin) expressed in HEK293T cells by spectra-fluorophotometry analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2022
Entry Details Article
PubMed
TargetRetinoic acid receptor RXR-alpha(Human)
Xiamen University

Curated by ChEMBL
LigandPNGBDBM50430575(CHEMBL2337794)
Affinity DataIC50: 1.07E+4nMAssay Description:Displacement of [3H]-9-cis-RA from human GST-tagged N-terminal truncated RXRalpha after 1 hr by liquid scintillation countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed