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

CHEMBL666358

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

Binding
Binding affinity at rat striatal Dopamine receptor D1 using [3H]- SCH-23390 radioligand
11
Total Activities
11
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 dopamine receptor affinities of enantiomers of 2-substituted apomorphines and their N-n-propyl analogues.
Gao YG, Baldessarini RJ, Kula NS, Neumeyer JL.
J Med Chem (1990) 33 : 1800 -1805
PubMed 1971309 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 11 6.30 7.13

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL431946 1 7.13
CHEMBL276326 1 6.97
CHEMBL53 APOMORPHINE 4.0 1 6.63
CHEMBL225230 R-N-PROPYLNORAPOMORPHINE 1 6.47
CHEMBL19130 1 6.10
CHEMBL54183 1 6.07
CHEMBL288096 1 6.04
CHEMBL53294 1 5.75
CHEMBL416288 (S)APOMORPHINE 1 5.53
CHEMBL53445 1 -
CHEMBL301761 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL431946 Ki = 74.5 nM 7.13
CHEMBL276326 Ki = 106.0 nM 6.97
CHEMBL53 APOMORPHINE Ki = 236.0 nM 6.63
CHEMBL225230 R-N-PROPYLNORAPOMORPHINE Ki = 340.0 nM 6.47
CHEMBL19130 Ki = 800.0 nM 6.10
CHEMBL54183 Ki = 851.0 nM 6.07
CHEMBL288096 Ki = 915.0 nM 6.04
CHEMBL53294 Ki = 1780.0 nM 5.75
CHEMBL416288 (S)APOMORPHINE Ki = 2980.0 nM 5.53
CHEMBL53445 Ki < 10000.0 nM -
CHEMBL301761 Ki < 10000.0 nM -