Compile Data Set for Download or QSAR
Report error Found 50 Enz. Inhib. hit(s) with all data for entry = 50002967
LigandPNGBDBM50025079([4-(2-Amino-propyl)-3-methyl-phenyl]-dimethyl-amin...)
Affinity DataIC50: 100nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025080(1-(4-Chloro-2,3-dihydro-1H-indol-5-ylmethyl)-propy...)
Affinity DataIC50: 300nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025084(2-(1-Ethyl-6-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 330nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025081(2-(2,3-Dihydro-1H-indol-5-yl)-1-methyl-ethylamine ...)
Affinity DataIC50: 360nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025086(1-Methyl-2-(4-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 380nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025077(1-(2,3-Dihydro-1H-indol-5-ylmethyl)-propylamine | ...)
Affinity DataIC50: 500nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025080(1-(4-Chloro-2,3-dihydro-1H-indol-5-ylmethyl)-propy...)
Affinity DataIC50: 630nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025079([4-(2-Amino-propyl)-3-methyl-phenyl]-dimethyl-amin...)
Affinity DataIC50: 650nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025086(1-Methyl-2-(4-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 750nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025086(1-Methyl-2-(4-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 800nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025079([4-(2-Amino-propyl)-3-methyl-phenyl]-dimethyl-amin...)
Affinity DataIC50: 800nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025085(2-(1-Ethyl-4-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 1.10E+3nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025080(1-(4-Chloro-2,3-dihydro-1H-indol-5-ylmethyl)-propy...)
Affinity DataIC50: 1.45E+3nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025085(2-(1-Ethyl-4-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 1.50E+3nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025080(1-(4-Chloro-2,3-dihydro-1H-indol-5-ylmethyl)-propy...)
Affinity DataIC50: 1.60E+3nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025081(2-(2,3-Dihydro-1H-indol-5-yl)-1-methyl-ethylamine ...)
Affinity DataIC50: 1.80E+3nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025083(2-(2,3-Dihydro-1H-indol-5-yl)-1,1-dimethyl-ethylam...)
Affinity DataIC50: 1.90E+3nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025084(2-(1-Ethyl-6-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 2.20E+3nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025084(2-(1-Ethyl-6-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 2.50E+3nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025083(2-(2,3-Dihydro-1H-indol-5-yl)-1,1-dimethyl-ethylam...)
Affinity DataIC50: 2.70E+3nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025083(2-(2,3-Dihydro-1H-indol-5-yl)-1,1-dimethyl-ethylam...)
Affinity DataIC50: 2.80E+3nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025077(1-(2,3-Dihydro-1H-indol-5-ylmethyl)-propylamine | ...)
Affinity DataIC50: 3.60E+3nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025081(2-(2,3-Dihydro-1H-indol-5-yl)-1-methyl-ethylamine ...)
Affinity DataIC50: 3.80E+3nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025081(2-(2,3-Dihydro-1H-indol-5-yl)-1-methyl-ethylamine ...)
Affinity DataIC50: 5.00E+3nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025078(1-Methyl-2-(6-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 6.00E+3nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025078(1-Methyl-2-(6-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 6.00E+3nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransporter(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50025085(2-(1-Ethyl-4-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 7.50E+3nMAssay Description:In vitro inhibition of NE uptake at NE uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025086(1-Methyl-2-(4-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 9.00E+3nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025080(1-(4-Chloro-2,3-dihydro-1H-indol-5-ylmethyl)-propy...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025077(1-(2,3-Dihydro-1H-indol-5-ylmethyl)-propylamine | ...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025083(2-(2,3-Dihydro-1H-indol-5-yl)-1,1-dimethyl-ethylam...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025085(2-(1-Ethyl-4-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025079([4-(2-Amino-propyl)-3-methyl-phenyl]-dimethyl-amin...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025084(2-(1-Ethyl-6-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vivo inhibition of DA uptake at dopamine uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025078(1-Methyl-2-(6-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 1.30E+4nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025077(1-(2,3-Dihydro-1H-indol-5-ylmethyl)-propylamine | ...)
Affinity DataIC50: 1.40E+4nMAssay Description:Compound was tested in vitro for inhibition of Monoamino oxidase by using [14C]5-HT as substrate in rat brain mitochondrial preparationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025078(1-Methyl-2-(6-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 1.60E+4nMAssay Description:Compound was tested in vitro for inhibition of Serotonin transporter uptake at serotonin uptake siteMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025084(2-(1-Ethyl-6-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 7.70E+4nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025081(2-(2,3-Dihydro-1H-indol-5-yl)-1-methyl-ethylamine ...)
Affinity DataIC50: 1.00E+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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025078(1-Methyl-2-(6-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 1.70E+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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025086(1-Methyl-2-(4-methyl-2,3-dihydro-1H-indol-5-yl)-et...)
Affinity DataIC50: 5.00E+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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025085(2-(1-Ethyl-4-methyl-2,3-dihydro-1H-indol-5-yl)-1-m...)
Affinity DataIC50: 5.00E+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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025077(1-(2,3-Dihydro-1H-indol-5-ylmethyl)-propylamine | ...)
Affinity DataIC50: 8.00E+5nMAssay Description:Compound was tested in vitro for inhibition of Monoamino oxidase by using [14C]phenylethylamine as substrate in rat brain mitochondrial preparationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025079([4-(2-Amino-propyl)-3-methyl-phenyl]-dimethyl-amin...)
Affinity DataIC50: 1.00E+6nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50025083(2-(2,3-Dihydro-1H-indol-5-yl)-1,1-dimethyl-ethylam...)
Affinity DataIC50: 2.60E+6nMAssay 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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed