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Assay Detail

CHEMBL672016

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

Binding
Binding affinity for rat striatum Dopamine receptor D1 by [3H]-SCH- -2339 displacement.
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

D(1A) dopamine receptor (CHEMBL265)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Synthesis and pharmacological evaluation of potent and highly selective D3 receptor ligands: inhibition of cocaine-seeking behavior and the role of dopamine D3/D2 receptors.
Campiani G, Butini S, Trotta F, Fattorusso C, Catalanotti B, Aiello F, Gemma S, Nacci V, Novellino E, Stark JA, Cagnotto A, Fumagalli E, Carnovali F, Cervo L, Mennini T.
J Med Chem (2003) 46 : 3822 -3839
PubMed 12930145 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 16 5.68 6.11

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL126590 1 6.11
CHEMBL125916 1 6.01
CHEMBL127317 1 5.87
CHEMBL127344 1 5.84
CHEMBL127400 1 5.83
CHEMBL420510 1 5.80
CHEMBL125193 1 5.78
CHEMBL124444 1 5.59
CHEMBL2112643 1 5.57
CHEMBL25236 BP-897 1 5.52
CHEMBL435218 1 5.12
CHEMBL340641 1 5.11
CHEMBL123952 1 -
CHEMBL339960 1 -
CHEMBL126889 1 -
CHEMBL341117 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL126590 Ki = 778.0 nM 6.11
CHEMBL125916 Ki = 970.0 nM 6.01
CHEMBL127317 Ki = 1350.0 nM 5.87
CHEMBL127344 Ki = 1440.0 nM 5.84
CHEMBL127400 Ki = 1480.0 nM 5.83
CHEMBL420510 Ki = 1567.0 nM 5.80
CHEMBL125193 Ki = 1655.0 nM 5.78
CHEMBL124444 Ki = 2565.0 nM 5.59
CHEMBL2112643 Ki = 2676.0 nM 5.57
CHEMBL25236 BP-897 Ki = 3000.0 nM 5.52
CHEMBL435218 Ki = 7664.0 nM 5.12
CHEMBL340641 Ki = 7750.0 nM 5.11
CHEMBL123952 Ki > 10000.0 nM -
CHEMBL339960 Ki > 10000.0 nM -
CHEMBL126889 Ki > 10000.0 nM -
CHEMBL341117 Ki > 10000.0 nM -