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

CHEMBL673374

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

Binding
In vitro binding affinity was measured by displacement of [3H]- raclopride from D2 receptor isolated from the striata of male Dawley rats
18
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

D(2) dopamine receptor (CHEMBL339)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Cyclic benzamides as mixed dopamine D2/serotonin 5-HT2 receptor antagonists: potential atypical antipsychotic agents.
Norman MH, Rigdon GC, Navas F, Cooper BR.
J Med Chem (1994) 37 : 2552 -2563
PubMed 7914539 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 7.49 8.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL83625 2 8.80
CHEMBL83195 1 8.30
CHEMBL315925 1 8.28
CHEMBL86013 1 8.24
CHEMBL87294 1 7.96
CHEMBL314370 1 7.77
CHEMBL83510 1 7.64
CHEMBL314043 1 7.57
CHEMBL85647 1 7.50
CHEMBL54 HALOPERIDOL 4.0 1 7.40
CHEMBL41626 1 7.37
CHEMBL290937 1 7.31
CHEMBL83454 1 7.03
CHEMBL85137 1 6.66
CHEMBL42 CLOZAPINE 4.0 1 6.54
CHEMBL3144650 1 6.30
CHEMBL314684 1 6.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL83625 IC50 = 1.6 nM 8.80
CHEMBL83195 IC50 = 5.0 nM 8.30
CHEMBL315925 IC50 = 5.2 nM 8.28
CHEMBL86013 IC50 = 5.8 nM 8.24
CHEMBL83625 IC50 = 10.0 nM 8.00
CHEMBL87294 IC50 = 11.0 nM 7.96
CHEMBL314370 IC50 = 17.0 nM 7.77
CHEMBL83510 IC50 = 23.0 nM 7.64
CHEMBL314043 IC50 = 27.0 nM 7.57
CHEMBL85647 IC50 = 32.0 nM 7.50
CHEMBL54 HALOPERIDOL IC50 = 40.0 nM 7.40
CHEMBL41626 IC50 = 43.0 nM 7.37
CHEMBL290937 IC50 = 49.0 nM 7.31
CHEMBL83454 IC50 = 94.0 nM 7.03
CHEMBL85137 IC50 = 220.0 nM 6.66
CHEMBL42 CLOZAPINE IC50 = 290.0 nM 6.54
CHEMBL3144650 IC50 = 500.0 nM 6.30
CHEMBL314684 IC50 = 600.0 nM 6.22