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Assay Detail

CHEMBL666362

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

Binding
Binding affinity was determined by measuring the ability to displace [125I]SCH-23982 from Dopamine receptor D1 in rat caudate (in vitro)
10
Total Activities
5
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

(1R,3S)-1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-3-phenyl-1H-2-benzopyran: a potent and selective D1 agonist.
DeNinno MP, Schoenleber R, Asin KE, MacKenzie R, Kebabian JW.
J Med Chem (1990) 33 : 2948 -2950
PubMed 1977907 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 7.13 8.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL86931 4 8.80
CHEMBL286080 SKF-38393 2 7.19
CHEMBL99361 1 5.99
CHEMBL542683 1 5.99
CHEMBL83080 2 5.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL86931 Ki = 1.6 nM 8.80
CHEMBL86931 Ki = 1.6 nM 8.80
CHEMBL86931 Ki = 3.0 nM 8.52
CHEMBL86931 Ki = 3.0 nM 8.52
CHEMBL286080 SKF-38393 Ki = 64.1 nM 7.19
CHEMBL286080 SKF-38393 Ki = 64.0 nM 7.19
CHEMBL99361 Ki = 1030.0 nM 5.99
CHEMBL542683 Ki = 1030.0 nM 5.99
CHEMBL83080 Ki = 7200.0 nM 5.14
CHEMBL83080 Ki = 7200.0 nM 5.14