Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL4039190

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

Binding
Inhibition of human dopamine D4 receptor
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Return of D4 Dopamine Receptor Antagonists in Drug Discovery.
Lindsley CW, Hopkins CR.
J Med Chem (2017) 60 : 7233 -7243
PubMed 28489950 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 8.46 9.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4096543 1 9.48
CHEMBL267014 L-745870 1 9.37
CHEMBL127257 1 8.82
CHEMBL320597 1 8.70
CHEMBL54 HALOPERIDOL 4.0 1 8.64
CHEMBL444309 1 8.60
CHEMBL4080034 1 8.55
CHEMBL81330 1 8.52
CHEMBL69759 SONEPIPRAZOLE 2.0 1 8.44
CHEMBL305276 1 8.40
CHEMBL4066603 1 8.31
CHEMBL4104272 1 8.25
CHEMBL126429 1 8.22
CHEMBL4069306 1 8.21
CHEMBL4095082 1 8.06
CHEMBL42 CLOZAPINE 4.0 1 8.00
CHEMBL303692 1 7.23

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4096543 Ki = 0.33 nM 9.48
CHEMBL267014 L-745870 Ki = 0.43 nM 9.37
CHEMBL127257 Ki = 1.5 nM 8.82
CHEMBL320597 Ki = 2.0 nM 8.70
CHEMBL54 HALOPERIDOL Ki = 2.3 nM 8.64
CHEMBL444309 Ki = 2.5 nM 8.60
CHEMBL4080034 Ki = 2.8 nM 8.55
CHEMBL81330 Ki = 3.0 nM 8.52
CHEMBL69759 SONEPIPRAZOLE Ki = 3.6 nM 8.44
CHEMBL305276 Ki = 4.0 nM 8.40
CHEMBL4066603 Ki = 4.9 nM 8.31
CHEMBL4104272 Ki = 5.6 nM 8.25
CHEMBL126429 Ki = 6.0 nM 8.22
CHEMBL4069306 Ki = 6.2 nM 8.21
CHEMBL4095082 Ki = 8.8 nM 8.06
CHEMBL42 CLOZAPINE Ki = 10.0 nM 8.00
CHEMBL303692 Ki = 59.0 nM 7.23