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Assay Detail

CHEMBL4357658

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

Binding
Inhibition of human cathepsin D
16
Total Activities
16
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 D (CHEMBL2581)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Plasmepsin Inhibitors in Antimalarial Drug Discovery: Medicinal Chemistry and Target Validation (2000 to Present).
Cheuka PM, Dziwornu G, Okombo J, Chibale K.
J Med Chem (2020) 63 : 4445 -4467
PubMed 31913032 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.36 8.05
Ki 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL257594 1 8.05
CHEMBL121769 1 5.89
CHEMBL4556003 1 5.70
CHEMBL4541926 1 5.69
CHEMBL558459 HYDRAZOBENZENE 1 5.62
CHEMBL4580614 1 5.36
CHEMBL4444927 1 5.28
CHEMBL4448566 1 5.16
CHEMBL4581955 1 4.82
CHEMBL4518375 1 4.74
CHEMBL1233569 1 4.69
CHEMBL4225824 1 4.68
CHEMBL4469961 1 4.06
CHEMBL176888 1 -
CHEMBL1233097 1 -
CHEMBL4554448 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL257594 IC50 = 9.0 nM 8.05
CHEMBL121769 IC50 = 1300.0 nM 5.89
CHEMBL4556003 IC50 = 1997.0 nM 5.70
CHEMBL4541926 IC50 = 2030.0 nM 5.69
CHEMBL558459 HYDRAZOBENZENE IC50 = 2400.0 nM 5.62
CHEMBL4580614 IC50 = 4400.0 nM 5.36
CHEMBL4444927 IC50 = 5200.0 nM 5.28
CHEMBL4448566 IC50 = 7000.0 nM 5.16
CHEMBL4581955 IC50 = 15000.0 nM 4.82
CHEMBL4518375 IC50 = 18300.0 nM 4.74
CHEMBL1233569 IC50 = 20362.0 nM 4.69
CHEMBL4225824 IC50 = 21000.0 nM 4.68
CHEMBL4469961 IC50 = 87000.0 nM 4.06
CHEMBL176888 Ki > 200.0 nM -
CHEMBL1233097 IC50 > 1300000.0 nM -
CHEMBL4554448 IC50 = 262000.0 nM -