Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL672018

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Binding affinity towards dopamine receptor D1 using [3H]SCH-23390 was determined in rat striatal membranes
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Tissue Striatum
Subcellular Membrane
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 15 6.90 9.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL62 SCH-23390 1 9.40
CHEMBL303993 1 8.18
CHEMBL334350 1 8.08
CHEMBL336218 1 6.86
CHEMBL299056 1 6.76
CHEMBL300778 1 6.75
CHEMBL135318 1 6.43
CHEMBL293158 1 6.36
CHEMBL57988 1 6.25
CHEMBL446396 1 6.13
CHEMBL323771 1 6.08
CHEMBL445129 1 5.57
CHEMBL434809 1 -
CHEMBL137420 1 -
CHEMBL109723 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL62 SCH-23390 Ki = 0.4 nM 9.40
CHEMBL303993 Ki = 6.6 nM 8.18
CHEMBL334350 Ki = 8.3 nM 8.08
CHEMBL336218 Ki = 138.0 nM 6.86
CHEMBL299056 Ki = 174.0 nM 6.76
CHEMBL300778 Ki = 179.0 nM 6.75
CHEMBL135318 Ki = 370.0 nM 6.43
CHEMBL293158 Ki = 442.0 nM 6.36
CHEMBL57988 Ki = 565.0 nM 6.25
CHEMBL446396 Ki = 743.0 nM 6.13
CHEMBL323771 Ki = 830.0 nM 6.08
CHEMBL445129 Ki = 2700.0 nM 5.57
CHEMBL434809 Ki > 5000.0 nM -
CHEMBL137420 Ki > 5000.0 nM -
CHEMBL109723 Ki > 5000.0 nM -