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Found 15 Enz. Inhib. hit(s) with all data for entry = 50035777
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017519(1,1-Diethyl-3-(7-methyl-4,6,6a,7,8,9,10,10a-octahy...)
Affinity DataIC50:  4nMAssay Description:In vitro binding activity against dopamine receptor D2 from homogenized rat brain, using [3H]spiperone as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM21393(7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-o...)
Affinity DataIC50:  4.5nMAssay Description:In vitro binding activity against 5-hydroxytryptamine 1A receptor receptor from homogenized rat brain, using [3H]8-OH-DPAT as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017519(1,1-Diethyl-3-(7-methyl-4,6,6a,7,8,9,10,10a-octahy...)
Affinity DataIC50:  25nMAssay Description:In vitro binding activity against 5-hydroxytryptamine 1A receptor from homogenized rat brain, using [3H]-8-OH-DPAT as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044236(CHEMBL303339 | Dimethyl-(R)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  31nMAssay Description:In vitro binding activity against 5-hydroxytryptamine 1A receptor from homogenized rat brain, using [3H]8-OH-DPAT as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017519(1,1-Diethyl-3-(7-methyl-4,6,6a,7,8,9,10,10a-octahy...)
Affinity DataIC50:  69nMAssay Description:In vitro binding activity against Dopamine receptor D1 from homogenized rat brain, using [3H]SCH-23390 as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017520((+/-)-Dimethyl-(6,7,8,9-tetrahydro-3H-benzo[e]indo...)
Affinity DataIC50:  82nMAssay Description:In vitro binding activity against 5-hydroxytryptamine 1A receptor from homogenized rat brain, using [3H]8-OH-DPAT as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044235(CHEMBL292274 | Dimethyl-(S)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  244nMAssay Description:In vitro binding activity against 5-hydroxytryptamine 1A receptor from homogenized rat brain, using [3H]8-OH-DPAT as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044236(CHEMBL303339 | Dimethyl-(R)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  1.05E+3nMAssay Description:In vitro binding activity against dopamine receptor D2 from homogenized rat brain, using [3H]spiperone as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017520((+/-)-Dimethyl-(6,7,8,9-tetrahydro-3H-benzo[e]indo...)
Affinity DataIC50:  1.84E+3nMAssay Description:In vitro binding activity against dopamine receptor D2 from homogenized rat brain, using [3H]spiperone as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM21393(7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-o...)
Affinity DataIC50:  5.76E+3nMAssay Description:In vitro binding activity against Dopamine receptor D2 from homogenized rat brain, using [3H]spiperone as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044235(CHEMBL292274 | Dimethyl-(S)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  9.51E+3nMAssay Description:In vitro binding activity against dopamine receptor D2 from homogenized rat brain, using [3H]spiperone as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50017520((+/-)-Dimethyl-(6,7,8,9-tetrahydro-3H-benzo[e]indo...)
Affinity DataIC50:  1.97E+4nMAssay Description:In vitro binding activity against dopamine receptor D1 from homogenized rat brain, using [3H]SCH-23390 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044236(CHEMBL303339 | Dimethyl-(R)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  2.04E+4nMAssay Description:In vitro binding activity against dopamine receptor D1 from homogenized rat brain, using [3H]SCH-23390 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM50044235(CHEMBL292274 | Dimethyl-(S)-6,7,8,9-tetrahydro-3H-...)
Affinity DataIC50:  2.92E+4nMAssay Description:In vitro binding activity against dopamine receptor D1 from homogenized rat brain, using [3H]SCH-23390 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
University Of G£Teborg

Curated by ChEMBL
LigandPNGBDBM21393(7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-o...)
Affinity DataIC50: >1.00E+5nMAssay Description:In vitro binding activity against dopamine D1 receptor from homogenized rat brain, using [3H]SCH-23390 as the radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed