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Assay Detail

CHEMBL1670880

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

Binding
Inhibition of human recombinant cathepsin V expressed in Pichia pastoris by Lineweaver-Burk double-reciprocal plots
9
Total Activities
9
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

Acridone alkaloids as potent inhibitors of cathepsin V.
Severino RP, Guido RV, Marques EF, Brömme D, da Silva MF, Fernandes JB, Andricopulo AD, Vieira PC.
Bioorg Med Chem (2011) 19 : 1477 -1481
PubMed 21277783 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 9 5.82 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1668599 CITIBRASINE 1 6.70
CHEMBL1668597 1 6.30
CHEMBL451705 CITRUSININE-I 1 6.00
CHEMBL463652 GLYCOCITRINE-IV 1 5.96
CHEMBL464846 1 5.92
CHEMBL1668602 1 5.77
CHEMBL465847 CITRUSININE-II 1 5.38
CHEMBL1668601 1 5.36
CHEMBL1668598 GLYCOCITRINE-I 1 5.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1668599 CITIBRASINE Ki = 200.0 nM 6.70
CHEMBL1668597 Ki = 500.0 nM 6.30
CHEMBL451705 CITRUSININE-I Ki = 1000.0 nM 6.00
CHEMBL463652 GLYCOCITRINE-IV Ki = 1100.0 nM 5.96
CHEMBL464846 Ki = 1200.0 nM 5.92
CHEMBL1668602 Ki = 1700.0 nM 5.77
CHEMBL465847 CITRUSININE-II Ki = 4200.0 nM 5.38
CHEMBL1668601 Ki = 4400.0 nM 5.36
CHEMBL1668598 GLYCOCITRINE-I Ki = 10000.0 nM 5.00