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Assay Detail

CHEMBL949948

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

Binding
Inhibition of human recombinant cathepsin S
18
Total Activities
18
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Cathepsin S (CHEMBL2954)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality.
Maryanoff BE, Costanzo MJ.
Bioorg Med Chem (2008) 16 : 1562 -1595
PubMed 18053726 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 5.95 7.52
IC50 1 8.18 8.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL256191 1 8.18
CHEMBL257692 1 7.52
CHEMBL446718 1 7.40
CHEMBL379622 1 6.50
CHEMBL209215 1 6.46
CHEMBL272374 1 6.42
CHEMBL405602 1 6.33
CHEMBL411498 1 5.70
CHEMBL208566 1 5.48
CHEMBL210198 1 4.70
CHEMBL272375 1 4.58
CHEMBL211050 1 4.35
CHEMBL262621 1 -
CHEMBL271004 1 -
CHEMBL255982 1 -
CHEMBL403019 1 -
CHEMBL401781 1 -
CHEMBL260818 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL256191 IC50 = 6.6 nM 8.18
CHEMBL257692 Ki = 30.0 nM 7.52
CHEMBL446718 Ki = 40.0 nM 7.40
CHEMBL379622 Ki = 320.0 nM 6.50
CHEMBL209215 Ki = 350.0 nM 6.46
CHEMBL272374 Ki = 380.0 nM 6.42
CHEMBL405602 Ki = 470.0 nM 6.33
CHEMBL411498 Ki = 2000.0 nM 5.70
CHEMBL208566 Ki = 3300.0 nM 5.48
CHEMBL210198 Ki = 20000.0 nM 4.70
CHEMBL272375 Ki = 26000.0 nM 4.58
CHEMBL211050 Ki = 45000.0 nM 4.35
CHEMBL262621 Ki < 100.0 nM -
CHEMBL271004 Ki < 0.25 nM -
CHEMBL255982 Ki < 10.0 nM -
CHEMBL403019 Ki < 100.0 nM -
CHEMBL401781 Ki < 100.0 nM -
CHEMBL260818 Ki < 100.0 nM -