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Assay Detail

CHEMBL676504

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

Binding
In vitro ability to inhibit the binding of [3H]spiperone to cloned human dopamine receptor D4 using apomorphine induced climbing test in male Swiss mice
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

D(4) dopamine receptor (CHEMBL219)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

The acute EPS of haloperidol may be unrelated to its metabolic transformation to BCPP+.
Sikazwe DM, Li S, Lyles-Eggleston M, Ablordeppey SY.
Bioorg Med Chem Lett (2003) 13 : 3779 -3782
PubMed 14552778 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 3 7.73 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL54 HALOPERIDOL 4.0 1 8.00
CHEMBL210578 1 7.92
CHEMBL42 CLOZAPINE 4.0 1 7.27

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL54 HALOPERIDOL Ki = 10.0 nM 8.00
CHEMBL210578 Ki = 12.0 nM 7.92
CHEMBL42 CLOZAPINE Ki = 54.0 nM 7.27