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Assay Detail

CHEMBL2327671

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

Binding
Inhibition of rat VAP1 expressed in CHO cells using [14C]-benzylamine as substrate incubated for 30 mins prior to substrate addition measured after 1 hr by scintillation spectrophotometric analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Cell Type CHO
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Amine oxidase [copper-containing] 3 (CHEMBL4592)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Synthesis and SAR study of new thiazole derivatives as vascular adhesion protein-1 (VAP-1) inhibitors for the treatment of diabetic macular edema.
Inoue T, Morita M, Tojo T, Yoshihara K, Nagashima A, Moritomo A, Ohkubo M, Miyake H.
Bioorg Med Chem (2013) 21 : 1219 -1233
PubMed 23337801 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.85 7.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2326864 1 7.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2326864 IC50 = 14.0 nM 7.85