BDBM50048111 (2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide::CHEMBL57283

SMILES C[N+](C)(C)c1cccc(O)c1O

InChI Key InChIKey=ADEICXSVFWLTKN-UHFFFAOYSA-O

Data  3 KI  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50048111   

TargetSodium-dependent serotonin transporter(Rat)
University of Toledo

Curated by ChEMBL
LigandPNGBDBM50048111((2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide ...)
Affinity DataIC50: 2.13E+5nMAssay Description:Inhibition constant of high-affinity 5-HT uptakeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium- and chloride-dependent creatine transporter 1(Rat)
University of Toledo

Curated by ChEMBL
LigandPNGBDBM50048111((2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide ...)
Affinity DataIC50: 8.30E+4nMAssay Description:Inhibition of high affinity choline uptake at concentration of 1 uMMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium- and chloride-dependent creatine transporter 1(Rat)
University of Toledo

Curated by ChEMBL
LigandPNGBDBM50048111((2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide ...)
Affinity DataKi:  6.00E+4nMAssay Description:Inhibition constant of high-affinity choline uptakeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent serotonin transporter(Rat)
University of Toledo

Curated by ChEMBL
LigandPNGBDBM50048111((2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide ...)
Affinity DataKi:  9.00E+4nMAssay Description:Inhibition constant of high-affinity 5-HT uptakeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholine O-acetyltransferase(Rat)
University of Toledo

Curated by ChEMBL
LigandPNGBDBM50048111((2,3-Dihydroxy-phenyl)-trimethyl-ammonium; iodide ...)
Affinity DataKi:  1.50E+7nMAssay Description:Enzyme inhibition dissociation constant for choline acetyl transferase (ChAcT) was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed