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Assay Detail

CHEMBL661836

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

Binding
Inhibition by displacing [3H]CCK-8S against human Cholecystokinin type B receptor
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Gastrin/cholecystokinin type B receptor (CHEMBL298)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and SAR of new 5-phenyl-3-ureido-1,5-benzodiazepines as cholecystokinin-B receptor antagonists.
Ursini A, Capelli AM, Carr RA, Cassarà P, Corsi M, Curcuruto O, Curotto G, Dal Cin M, Davalli S, Donati D, Feriani A, Finch H, Finizia G, Gaviraghi G, Marien M, Pentassuglia G, Polinelli S, Ratti E, Reggiani AM, Tarzia G, Tedesco G, Tranquillini ME, Trist DG, Van Amsterdam FT.
J Med Chem (2000) 43 : 3596 -3613
PubMed 11020274 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 8.80 9.45

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2062154 CI-988 1.0 1 9.45
CHEMBL330977 1 9.43
CHEMBL9387 L-365260 1 8.80
CHEMBL9506 DEVAZEPIDE 2.0 1 7.53

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2062154 CI-988 Ki = 0.3548 nM 9.45
CHEMBL330977 Ki = 0.3715 nM 9.43
CHEMBL9387 L-365260 Ki = 1.585 nM 8.80
CHEMBL9506 DEVAZEPIDE Ki = 29.51 nM 7.53