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Assay Detail

CHEMBL2379702

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

Binding
Displacement of [3H]histamine from human histamine H1 receptor expressed in HEK cells
5
Total Activities
5
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Histamine H1 receptor (CHEMBL231)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A novel series of histamine H4 receptor antagonists based on the pyrido[3,2-d]pyrimidine scaffold: comparison of hERG binding and target residence time with PF-3893787.
Andaloussi M, Lim HD, van der Meer T, Sijm M, Poulie CB, de Esch IJ, Leurs R, Smits RA.
Bioorg Med Chem Lett (2013) 23 : 2663 -2670
PubMed 23558237 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 4.72 4.95
pKi 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2376801 1 4.95
CHEMBL2376803 1 4.78
CHEMBL2376804 1 4.68
CHEMBL2376800 1 4.47
CHEMBL1915540 ADRIFORANT 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2376801 Ki = 11220.18 nM 4.95
CHEMBL2376803 Ki = 16595.87 nM 4.78
CHEMBL2376804 Ki = 20892.96 nM 4.68
CHEMBL2376800 Ki = 33884.42 nM 4.47
CHEMBL1915540 ADRIFORANT pKi - -