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

CHEMBL895625

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

Binding
Displacement of [3H]LSD from human 5HT7 receptor expressed in CHO cells
12
Total Activities
12
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

5-hydroxytryptamine receptor 7 (CHEMBL3155)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs.
Lange JH, Reinders JH, Tolboom JT, Glennon JC, Coolen HK, Kruse CG.
J Med Chem (2007) 50 : 5103 -5108
PubMed 17880057 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 7.53 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL85 RISPERIDONE 4.0 1 9.00
CHEMBL708 ZIPRASIDONE 4.0 1 8.30
CHEMBL196514 1 8.10
CHEMBL42 CLOZAPINE 4.0 1 7.70
CHEMBL243712 AMISULPRIDE 4.0 1 7.60
CHEMBL71 CHLORPROMAZINE 4.0 1 7.50
CHEMBL1112 ARIPIPRAZOLE 4.0 1 7.20
CHEMBL716 QUETIAPINE 4.0 1 7.20
CHEMBL221692 ADOPRAZINE 2.0 1 7.20
CHEMBL715 OLANZAPINE 4.0 1 7.10
CHEMBL131495 1 7.00
CHEMBL54 HALOPERIDOL 4.0 1 6.50

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL85 RISPERIDONE Ki = 1.0 nM 9.00
CHEMBL708 ZIPRASIDONE Ki = 5.012 nM 8.30
CHEMBL196514 Ki = 7.943 nM 8.10
CHEMBL42 CLOZAPINE Ki = 19.95 nM 7.70
CHEMBL243712 AMISULPRIDE Ki = 25.12 nM 7.60
CHEMBL71 CHLORPROMAZINE Ki = 31.62 nM 7.50
CHEMBL1112 ARIPIPRAZOLE Ki = 63.1 nM 7.20
CHEMBL716 QUETIAPINE Ki = 63.1 nM 7.20
CHEMBL221692 ADOPRAZINE Ki = 63.1 nM 7.20
CHEMBL715 OLANZAPINE Ki = 79.43 nM 7.10
CHEMBL131495 Ki = 100.0 nM 7.00
CHEMBL54 HALOPERIDOL Ki = 316.23 nM 6.50