BDBM50275438 (+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole::(-)-5-(3-benzylpyrrolidin-3-yl)-1H-indole::5-(3-BENZYLPYRROLIDIN-3-YL)-1H-INDOLE (STRUCTURAL MIX)::5-(3-benzylpyrrolidin-3-yl)-1H-indole::CHEMBL487355

SMILES C(c1ccccc1)C1(CCNC1)c1ccc2[nH]ccc2c1

InChI Key InChIKey=UZKWACFLBGIUSH-UHFFFAOYSA-N

Data  7 KI  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 11 hits for monomerid = 50275438   

TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  6nMAssay Description:Inhibition of SERT (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  17nMAssay Description:Inhibition of NET (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  17nMAssay Description:Inhibition of NET (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  54nMAssay Description:Inhibition of SERT (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  54nMAssay Description:Inhibition of SERT (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  81nMAssay Description:Inhibition of DAT (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataKi:  81nMAssay Description:Inhibition of DAT (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of human ERG expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataIC50:  300nMAssay Description:Inhibition of CYP2D6 (unknown origin) by fluorescence based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin) by fluorescence based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50275438((+)-5-(3-benzylpyrrolidin-3-yl)-1H-indole | (-)-5-...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin) by fluorescence based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed