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Assay Detail

CHEMBL668243

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Binding
Binding affinity against dopamine receptor D1
18
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

D(1A) dopamine receptor (CHEMBL265)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Synthesis and molecular modeling of 1-phenyl-1,2,3,4-tetrahydroisoquinolines and related 5,6,8,9-tetrahydro-13bH-dibenzo[a,h]quinolizines as D1 dopamine antagonists.
Minor DL, Wyrick SD, Charifson PS, Watts VJ, Nichols DE, Mailman RB.
J Med Chem (1994) 37 : 4317 -4328
PubMed 7996543 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 18 7.25 9.37

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL62 SCH-23390 1 9.37
CHEMBL293158 2 8.18
CHEMBL137420 1 8.08
CHEMBL334350 1 8.08
CHEMBL303993 2 8.04
CHEMBL299056 2 7.06
CHEMBL446396 1 6.85
CHEMBL336218 1 6.85
CHEMBL300778 1 6.75
CHEMBL135318 1 6.73
CHEMBL57988 1 6.55
CHEMBL323771 1 6.38
CHEMBL445129 1 5.86
CHEMBL434809 1 -
CHEMBL109723 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL62 SCH-23390 Ki = 0.4266 nM 9.37
CHEMBL293158 Ki = 6.607 nM 8.18
CHEMBL137420 Ki = 8.318 nM 8.08
CHEMBL334350 Ki = 8.318 nM 8.08
CHEMBL303993 Ki = 9.12 nM 8.04
CHEMBL303993 Ki = 9.12 nM 8.04
CHEMBL299056 Ki = 87.1 nM 7.06
CHEMBL446396 Ki = 141.25 nM 6.85
CHEMBL336218 Ki = 141.25 nM 6.85
CHEMBL299056 Ki = 177.83 nM 6.75
CHEMBL300778 Ki = 177.83 nM 6.75
CHEMBL135318 Ki = 186.21 nM 6.73
CHEMBL57988 Ki = 281.84 nM 6.55
CHEMBL323771 Ki = 416.87 nM 6.38
CHEMBL293158 Ki = 446.68 nM 6.35
CHEMBL445129 Ki = 1380.38 nM 5.86
CHEMBL434809 Ki < 10000.0 nM -
CHEMBL109723 Ki < 10000.0 nM -