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

CHEMBL666364

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

Binding
Inhibition of [3H]SCH-23,390 binding to Dopamine receptor D1 at 0.25 nM
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Expert

Target

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

Publication

Synthesis and pharmacological characterization of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as dopamine receptor ligands.
Charifson PS, Wyrick SD, Hoffman AJ, Simmons RM, Bowen JP, McDougald DL, Mailman RB.
J Med Chem (1988) 31 : 1941 -1946
PubMed 3050089 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 7.31 9.37

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL62 SCH-23390 1 9.37
CHEMBL292418 1 8.63
CHEMBL303993 1 8.18
CHEMBL57579 1 7.90
CHEMBL71 CHLORPROMAZINE 4.0 1 7.30
CHEMBL60706 1 7.27
CHEMBL65397 1 6.85
CHEMBL299056 1 6.76
CHEMBL293828 1 6.75
CHEMBL293158 1 6.36
CHEMBL57988 1 6.25
CHEMBL1788322 1 6.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL62 SCH-23390 Ki = 0.43 nM 9.37
CHEMBL292418 Ki = 2.35 nM 8.63
CHEMBL303993 Ki = 6.6 nM 8.18
CHEMBL57579 Ki = 12.5 nM 7.90
CHEMBL71 CHLORPROMAZINE Ki = 50.0 nM 7.30
CHEMBL60706 Ki = 53.2 nM 7.27
CHEMBL65397 Ki = 140.0 nM 6.85
CHEMBL299056 Ki = 174.0 nM 6.76
CHEMBL293828 Ki = 179.0 nM 6.75
CHEMBL293158 Ki = 442.0 nM 6.36
CHEMBL57988 Ki = 565.0 nM 6.25
CHEMBL1788322 Ki = 743.0 nM 6.13