null

SMILES CCCCCOc1cc2ccccc2cc1C(O)CCCCCCC([O-])=O

InChI Key InChIKey=AUVXPLBVCZOPLN-UHFFFAOYSA-M

  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 = 50172810   

TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
CNRS UMR 6052

Curated by ChEMBL
LigandPNGBDBM50172810(CHEMBL199121 | Sodium; 8-hydroxy-8-(3-pentyloxy-na...)copy SMILEScopy InChI
Affinity DataKi:  969nMAssay Description:Binding affinity for human PPAR gamma construct expressed in bacteria with 3[H] rosiglitazoneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26Q1WS5PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
CNRS UMR 6052

Curated by ChEMBL
LigandPNGBDBM50172810(CHEMBL199121 | Sodium; 8-hydroxy-8-(3-pentyloxy-na...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+4nMAssay Description:In vitro effective concentration against human peroxisome proliferator activated receptor gamma/Gal4 in cell-based transactivation assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26Q1WS5PubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
CNRS UMR 6052

Curated by ChEMBL
LigandPNGBDBM50172810(CHEMBL199121 | Sodium; 8-hydroxy-8-(3-pentyloxy-na...)copy SMILEScopy InChI
Affinity DataEC50:  1.49E+3nMAssay Description:In vitro effective concentration against human peroxisome proliferator activated receptor alpha/Gal4 in transactivation assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26Q1WS5PubMed