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Assay Detail

CHEMBL671421

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

Binding
In vitro binding affinity is the ability to displace [3H]spiperone from human Dopamine receptor D2 expressed in CHO-K1 cells
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type CHO-K1
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

D(2) dopamine receptor (CHEMBL217)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and dopaminergic activity of pyridine analogs of 5-hydroxy-2-(di-n-propylamino)tetralin.
Glase SA, Corbin AE, Pugsley TA, Heffner TG, Wise LD.
J Med Chem (1995) 38 : 3132 -3137
PubMed 7636875 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 7.06 7.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL110888 1 7.77
CHEMBL273273 5-OH-DPAT 1 7.58
CHEMBL105977 1 6.57
CHEMBL105512 1 6.33
CHEMBL106047 1 -
CHEMBL105509 1 -
CHEMBL318740 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL110888 Ki = 17.1 nM 7.77
CHEMBL273273 5-OH-DPAT Ki = 26.0 nM 7.58
CHEMBL105977 Ki = 272.0 nM 6.57
CHEMBL105512 Ki = 462.0 nM 6.33
CHEMBL106047 Ki > 10000.0 nM -
CHEMBL105509 Ki > 3333.0 nM -
CHEMBL318740 Ki > 3333.0 nM -