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Assay Detail

CHEMBL676288

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

Binding
Binding affinity which represents concentration giving half-maximal inhibition of [3H]7-OH-DPAT binding to Dopamine receptor D3 in rat tissue homogenate
4
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

D(3) dopamine receptor (CHEMBL3138)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

New antipsychotic agents with serotonin and dopamine antagonist properties based on a pyrrolo[2,1-b][1,3]benzothiazepine structure.
Campiani G, Nacci V, Bechelli S, Ciani SM, Garofalo A, Fiorini I, Wikström H, de Boer P, Liao Y, Tepper PG, Cagnotto A, Mennini T.
J Med Chem (1998) 41 : 3763 -3772
PubMed 9748351 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 7.86 8.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL120512 2 8.39
CHEMBL59 DOPAMINE 4.0 1 7.96
CHEMBL333246 1 7.24

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL120512 Ki = 4.1 nM 8.39
CHEMBL59 DOPAMINE Ki = 11.0 nM 7.96
CHEMBL333246 Ki = 57.0 nM 7.24
CHEMBL120512 Ki = - nM -