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Assay Detail

CHEMBL2019577

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

Binding
Binding affinity to human bradykinin B1 receptor
20
Total Activities
20
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

B1 bradykinin receptor (CHEMBL4308)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Quinolinyl- and phenantridinyl-acetamides as bradykinin B1 receptor antagonists.
Eles J, Beke G, Vágó I, Bozó E, Huszár J, Tarcsay A, Kolok S, Schmidt E, Vastag M, Hornok K, Farkas S, Domány G, Keserű GM.
Bioorg Med Chem Lett (2012) 22 : 3095 -3099
PubMed 22483585 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 20 7.92 10.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL189123 1 10.47
CHEMBL2018866 1 9.00
CHEMBL2018871 1 8.92
CHEMBL2018873 1 8.77
CHEMBL2018861 1 8.66
CHEMBL2018868 1 8.54
CHEMBL2018867 1 8.51
CHEMBL2018865 1 8.42
CHEMBL2018863 1 8.37
CHEMBL2018869 1 8.33
CHEMBL2018859 1 8.20
CHEMBL2018874 1 8.05
CHEMBL2018872 1 8.04
CHEMBL2018870 1 7.81
CHEMBL2018864 1 6.86
CHEMBL2018862 1 6.78
CHEMBL2018860 1 6.32
CHEMBL2018858 1 6.32
CHEMBL2016601 1 6.20
CHEMBL2018857 1 5.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL189123 Ki = 0.034 nM 10.47
CHEMBL2018866 Ki = 1.0 nM 9.00
CHEMBL2018871 Ki = 1.2 nM 8.92
CHEMBL2018873 Ki = 1.7 nM 8.77
CHEMBL2018861 Ki = 2.2 nM 8.66
CHEMBL2018868 Ki = 2.9 nM 8.54
CHEMBL2018867 Ki = 3.1 nM 8.51
CHEMBL2018865 Ki = 3.8 nM 8.42
CHEMBL2018863 Ki = 4.3 nM 8.37
CHEMBL2018869 Ki = 4.7 nM 8.33
CHEMBL2018859 Ki = 6.3 nM 8.20
CHEMBL2018874 Ki = 8.9 nM 8.05
CHEMBL2018872 Ki = 9.1 nM 8.04
CHEMBL2018870 Ki = 15.5 nM 7.81
CHEMBL2018864 Ki = 138.0 nM 6.86
CHEMBL2018862 Ki = 166.0 nM 6.78
CHEMBL2018860 Ki = 481.0 nM 6.32
CHEMBL2018858 Ki = 480.0 nM 6.32
CHEMBL2016601 Ki = 628.0 nM 6.20
CHEMBL2018857 Ki = 1400.0 nM 5.85