null

SMILES OC(=O)CCCOc1ccc(cc1)-c1cc(OC(F)(F)F)ccc1Cl

InChI Key InChIKey=FGXVJHYCASUBMZ-UHFFFAOYSA-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 9 hits for monomerid = 50203654   

TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetFree fatty acid receptor 4(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataEC50:  57nMAssay Description:Agonist activity at human GPR120 expressed in CHOK1 cells measured after 60 mins by IP1-HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetFree fatty acid receptor 4(Mus musculus)
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataEC50:  9nMAssay Description:Agonist activity at mouse GPR120 expressed in CHOK1 cells measured after 60 mins by IP1-HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetSodium channel protein type 5 subunit alpha(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 1.74E+4nMAssay Description:Inhibition of Nav1.5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetFree fatty acid receptor 1(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataEC50:  1.04E+3nMAssay Description:Agonist activity at human GPR40 measured after 60 mins by IP1-HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Cav1.2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Merck& Co.

Curated by ChEMBL
LigandPNGBDBM50203654(CHEMBL3968947)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7WZ2PubMed