BDBM50025082 2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-ethylamine::CHEMBL31059

SMILES CC(N)Cc1ccc2NCCc2c1Cl

InChI Key InChIKey=UWEORUSMUYMWMZ-UHFFFAOYSA-N

Data  5 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 = 50025082   

TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50025082(2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-et...)
Affinity DataIC50: >1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransporter(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50025082(2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-et...)
Affinity DataIC50:  320nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A/B(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50025082(2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-et...)
Affinity DataIC50:  200nMAssay Description:Compound was tested in vitro for inhibition of MAO by using [14C]5-HT as substrate in rat brain mitochondrial preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A/B(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50025082(2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-et...)
Affinity DataIC50:  8.00E+5nMAssay Description:Compound was tested in vitro for inhibition of MAO by using [14C]phenylethylamine as substrate in rat brain mitochondrial preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50025082(2-(4-Chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-et...)
Affinity DataIC50:  340nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed