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Assay Detail

CHEMBL872394

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

Binding
In vitro inhibitory constant against [3H]spiperone binding to human dopamine D2 receptor expressed in CHO cells
33
Total Activities
33
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO
Confidence 9 — Direct single protein target
Curated By Expert

Target

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

Publication

Synthesis, structure-activity relationships, and biological properties of 1-heteroaryl-4-[omega-(1H-indol-3-yl)alkyl]piperazines, novel potential antipsychotics combining potent dopamine D2 receptor antagonism with potent serotonin reuptake inhibition.
Smid P, Coolen HK, Keizer HG, van Hes R, de Moes JP, den Hartog AP, Stork B, Plekkenpol RH, Niemann LC, Stroomer CN, Tulp MT, van Stuivenberg HH, McCreary AC, Hesselink MB, Herremans AH, Kruse CG.
J Med Chem (2005) 48 : 6855 -6869
PubMed 16250644 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 33 7.98 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL198224 1 9.00
CHEMBL198357 1 9.00
CHEMBL54 HALOPERIDOL 4.0 1 8.70
CHEMBL194240 1 8.68
CHEMBL198069 1 8.37
CHEMBL198070 1 8.35
CHEMBL370457 1 8.33
CHEMBL194844 1 8.29
CHEMBL196172 1 8.28
CHEMBL196514 1 8.16
CHEMBL199045 1 8.13
CHEMBL193854 1 8.09
CHEMBL198216 1 8.06
CHEMBL263329 1 8.04
CHEMBL196893 1 7.97
CHEMBL198107 1 7.97
CHEMBL198040 1 7.95
CHEMBL383396 1 7.94
CHEMBL369984 1 7.84
CHEMBL196132 1 7.82
CHEMBL197839 1 7.82
CHEMBL194510 1 7.81
CHEMBL372735 1 7.80
CHEMBL197665 1 7.75
CHEMBL193501 1 7.72
CHEMBL198812 1 7.69
CHEMBL196171 1 7.68
CHEMBL365605 1 7.62
CHEMBL370359 1 7.50
CHEMBL197943 1 7.45

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL198224 Ki = 1.0 nM 9.00
CHEMBL198357 Ki = 1.0 nM 9.00
CHEMBL54 HALOPERIDOL Ki = 2.0 nM 8.70
CHEMBL194240 Ki = 2.1 nM 8.68
CHEMBL198069 Ki = 4.3 nM 8.37
CHEMBL198070 Ki = 4.5 nM 8.35
CHEMBL370457 Ki = 4.7 nM 8.33
CHEMBL194844 Ki = 5.1 nM 8.29
CHEMBL196172 Ki = 5.3 nM 8.28
CHEMBL196514 Ki = 6.9 nM 8.16
CHEMBL199045 Ki = 7.4 nM 8.13
CHEMBL193854 Ki = 8.1 nM 8.09
CHEMBL198216 Ki = 8.7 nM 8.06
CHEMBL263329 Ki = 9.1 nM 8.04
CHEMBL198107 Ki = 10.7 nM 7.97
CHEMBL196893 Ki = 10.6 nM 7.97
CHEMBL198040 Ki = 11.3 nM 7.95
CHEMBL383396 Ki = 11.4 nM 7.94
CHEMBL369984 Ki = 14.6 nM 7.84
CHEMBL196132 Ki = 15.0 nM 7.82
CHEMBL197839 Ki = 15.0 nM 7.82
CHEMBL194510 Ki = 15.5 nM 7.81
CHEMBL372735 Ki = 15.9 nM 7.80
CHEMBL197665 Ki = 17.9 nM 7.75
CHEMBL193501 Ki = 19.0 nM 7.72
CHEMBL198812 Ki = 20.3 nM 7.69
CHEMBL196171 Ki = 21.0 nM 7.68
CHEMBL365605 Ki = 24.0 nM 7.62
CHEMBL370359 Ki = 31.6 nM 7.50
CHEMBL197943 Ki = 35.7 nM 7.45
CHEMBL196505 Ki = 45.0 nM 7.35
CHEMBL195015 Ki = 62.0 nM 7.21
CHEMBL198041 Ki = 90.0 nM 7.05