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Assay Detail

CHEMBL686763

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

Functional
Compound was evaluated for the ability to inhibit purified H+/K+ -ATPase at pH 7.4, by using gastric membrane vesicles prepared from hog stomach.
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Sus scrofa
Tissue Stomach
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Antiulcer agents. 5. Inhibition of gastric H+/K(+)-ATPase by substituted imidazo[1,2-a]pyridines and related analogues and its implication in modeling the high affinity potassium ion binding site of the gastric proton pump enzyme.
Kaminski JJ, Wallmark B, Briving C, Andersson BM.
J Med Chem (1991) 34 : 533 -541
PubMed 1847427 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.54 7.04

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL296482 1 7.04
CHEMBL64216 1 6.05
CHEMBL47529 1 5.80
CHEMBL296417 1 5.78
CHEMBL293244 1 5.70
CHEMBL296544 1 5.68
CHEMBL137700 1 5.07
CHEMBL43945 1 4.86
CHEMBL137742 1 4.85
CHEMBL45835 1 4.55
CHEMBL136140 1 -
CHEMBL46595 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL296482 IC50 = 92.0 nM 7.04
CHEMBL64216 IC50 = 890.0 nM 6.05
CHEMBL47529 IC50 = 1590.0 nM 5.80
CHEMBL296417 IC50 = 1680.0 nM 5.78
CHEMBL293244 IC50 = 2000.0 nM 5.70
CHEMBL296544 IC50 = 2100.0 nM 5.68
CHEMBL137700 IC50 = 8600.0 nM 5.07
CHEMBL43945 IC50 = 13700.0 nM 4.86
CHEMBL137742 IC50 = 14000.0 nM 4.85
CHEMBL45835 IC50 = 28400.0 nM 4.55
CHEMBL136140 IC50 = 206000.0 nM -
CHEMBL46595 IC50 = 178000.0 nM -