Compile Data Set for Download or QSAR
maximum 50k data
Found 31 Enz. Inhib. hit(s) with all data for entry = 50008887
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078250(CHEMBL39847 | Dipropyl-(8-thiophen-3-yl-chroman-3-...)
Affinity DataKi:  1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078242(CHEMBL41491 | [8-(2-Methoxy-phenyl)-chroman-3-yl]-...)
Affinity DataKi:  1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078243((8-Phenyl-chroman-3-yl)-dipropyl-amine | CHEMBL411...)
Affinity DataKi:  1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078240(CHEMBL41200 | [8-(4-Methoxy-phenyl)-chroman-3-yl]-...)
Affinity DataKi:  1.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50052869((R)-6-Methyl-11-phenyl-5,6,6a,7-tetrahydro-4H-dibe...)
Affinity DataKi:  1.80nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078244((3-Dipropylamino-chroman-8-yl)-phenyl-methanone | ...)
Affinity DataKi:  4nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078241((8-Furan-3-yl-chroman-3-yl)-dipropyl-amine | CHEMB...)
Affinity DataKi:  5.70nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078245((3-Dipropylamino-chroman-8-yl)-thiophen-3-yl-metha...)
Affinity DataKi:  7.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078247(1-[4-(3-Dipropylamino-chroman-8-carbonyl)-phenyl]-...)
Affinity DataKi:  11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078249((3-Dipropylamino-chroman-8-yl)-(4-methoxy-phenyl)-...)
Affinity DataKi:  11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078246((3-Dipropylamino-chroman-8-yl)-furan-3-yl-methanon...)
Affinity DataKi:  16nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078251((3-Dipropylamino-chroman-8-yl)-(4-trifluoromethyl-...)
Affinity DataKi:  47nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078241((8-Furan-3-yl-chroman-3-yl)-dipropyl-amine | CHEMB...)
Affinity DataKi:  48nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078252((3-Dipropylamino-chroman-8-yl)-(2-methoxy-phenyl)-...)
Affinity DataKi:  61nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078248(CHEMBL43073 | Dipropyl-(8-thiophen-3-yl-chroman-3-...)
Affinity DataKi:  64nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50036864(3-Dipropylamino-chroman-5-ol | CHEMBL27995)
Affinity DataKi:  83nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50020220(3-Dipropylamino-chroman-8-ol | CHEMBL38428)
Affinity DataKi:  128nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078250(CHEMBL39847 | Dipropyl-(8-thiophen-3-yl-chroman-3-...)
Affinity DataKi:  398nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078243((8-Phenyl-chroman-3-yl)-dipropyl-amine | CHEMBL411...)
Affinity DataKi:  590nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078248(CHEMBL43073 | Dipropyl-(8-thiophen-3-yl-chroman-3-...)
Affinity DataKi:  763nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078244((3-Dipropylamino-chroman-8-yl)-phenyl-methanone | ...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078245((3-Dipropylamino-chroman-8-yl)-thiophen-3-yl-metha...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078251((3-Dipropylamino-chroman-8-yl)-(4-trifluoromethyl-...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078242(CHEMBL41491 | [8-(2-Methoxy-phenyl)-chroman-3-yl]-...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078252((3-Dipropylamino-chroman-8-yl)-(2-methoxy-phenyl)-...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078247(1-[4-(3-Dipropylamino-chroman-8-carbonyl)-phenyl]-...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078249((3-Dipropylamino-chroman-8-yl)-(4-methoxy-phenyl)-...)
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078240(CHEMBL41200 | [8-(4-Methoxy-phenyl)-chroman-3-yl]-...)
Affinity DataKi:  1.09E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50078246((3-Dipropylamino-chroman-8-yl)-furan-3-yl-methanon...)
Affinity DataKi:  1.36E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50020220(3-Dipropylamino-chroman-8-ol | CHEMBL38428)
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50036864(3-Dipropylamino-chroman-5-ol | CHEMBL27995)
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed