null

SMILES CO[C@@H](Cc1ccc(cc1)C#CCCOc1ccc(Oc2ccccc2)cc1)C(O)=O

InChI Key InChIKey=PXPYSVWYMMGIEN-VWLOTQADSA-N

  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 8 hits for monomerid = 50157060   

TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataEC50:  1.88E+3nMAssay Description:Mean effective concentration against human peroxisome proliferator activated receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B30T6PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataEC50:  103nMAssay Description:Mean effective concentration against human peroxisome proliferator-activated receptor gammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B30T6PubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 3.94E+3nMAssay Description:Mean inhibitory concentration against human peroxisome proliferator-activated receptor deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B30T6PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Agonist activity at PPARgammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP54B4PubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+3nMAssay Description:Mean inhibitory concentration against human peroxisome proliferator activated receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B30T6PubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+3nMAssay Description:Agonist activity at PPARalphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP54B4PubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 3.94E+3nMAssay Description:Agonist activity at PPARdeltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP54B4PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50157060((S)-2-Methoxy-3-{4-[4-(4-phenoxy-phenoxy)-but-1-yn...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Mean inhibitory concentration against human peroxisome proliferator-activated receptor gammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B30T6PubMed