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Assay Detail

CHEMBL3382374

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

Binding
Inhibition of human cathepsin L using Z-Phe-Arg-pNA chromogenic substrate fluorogenic substrate incubated for 30 mins
5
Total Activities
5
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

Procathepsin L (CHEMBL3837)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

3-Cyano-3-aza-β-amino Acid Derivatives as Inhibitors of Human Cysteine Cathepsins.
Schmitz J, Beckmann AM, Dudic A, Li T, Sellier R, Bartz U, Gütschow M.
ACS Med Chem Lett (2014) 5 : 1076 -1081
PubMed 25313316 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 5 6.17 6.73

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3342185 1 6.73
CHEMBL3342184 1 6.64
CHEMBL3342183 1 6.24
CHEMBL3342186 1 5.77
CHEMBL371064 BALICATIB 2.0 1 5.49

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3342185 Ki = 185.0 nM 6.73
CHEMBL3342184 Ki = 228.0 nM 6.64
CHEMBL3342183 Ki = 573.0 nM 6.24
CHEMBL3342186 Ki = 1690.0 nM 5.77
CHEMBL371064 BALICATIB Ki = 3260.0 nM 5.49