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Assay Detail

CHEMBL679849

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

Binding
Inhibition of dopamine-stimulated adenylate cyclase obtained from rat corpus striatum was determined by the conversion of [32P]ATP to [32P]-cAMP
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

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 11 7.27 9.33

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL62 SCH-23390 1 9.33
CHEMBL292418 1 9.03
CHEMBL303993 1 8.18
CHEMBL60706 1 7.90
CHEMBL71 CHLORPROMAZINE 4.0 1 7.10
CHEMBL65397 1 6.96
CHEMBL293828 1 6.70
CHEMBL299056 1 6.69
CHEMBL293158 1 6.25
CHEMBL1788322 1 5.92
CHEMBL57988 1 5.90

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL62 SCH-23390 Ki = 0.47 nM 9.33
CHEMBL292418 Ki = 0.94 nM 9.03
CHEMBL303993 Ki = 6.58 nM 8.18
CHEMBL60706 Ki = 12.5 nM 7.90
CHEMBL71 CHLORPROMAZINE Ki = 79.0 nM 7.10
CHEMBL65397 Ki = 109.0 nM 6.96
CHEMBL293828 Ki = 202.0 nM 6.70
CHEMBL299056 Ki = 205.0 nM 6.69
CHEMBL293158 Ki = 568.0 nM 6.25
CHEMBL1788322 Ki = 1205.0 nM 5.92
CHEMBL57988 Ki = 1257.0 nM 5.90