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Assay Detail

CHEMBL3108103

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

Binding
Inhibition of human Cathepsin V using Z-Phe-Arg-aminomethylcoumarin as substrate preincubated for 30 mins followed by substrate addition
1
Total Activities
1
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

Cathepsin L2 (CHEMBL3272)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

The marine cyanobacterial metabolite gallinamide A is a potent and selective inhibitor of human cathepsin L.
Miller B, Friedman AJ, Choi H, Hogan J, McCammon JA, Hook V, Gerwick WH.
J Nat Prod (2014) 77 : 92 -99
PubMed 24364476 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.85 6.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL541700 GALLINAMIDE A 1 6.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL541700 GALLINAMIDE A IC50 = 140.0 nM 6.85