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Assay Detail

CHEMBL2384630

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

Binding
Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assay
19
Total Activities
19
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 B (CHEMBL4072)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Chalcones, inhibitors for topoisomerase I and cathepsin B and L, as potential anti-cancer agents.
Kim SH, Lee E, Baek KH, Kwon HB, Woo H, Lee ES, Kwon Y, Na Y.
Bioorg Med Chem Lett (2013) 23 : 3320 -3324
PubMed 23608763 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 4.77 7.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2368566 1 7.18
CHEMBL2382116 1 5.74
CHEMBL2382117 1 4.54
CHEMBL2382119 1 4.54
CHEMBL2382113 1 4.33
CHEMBL2382118 1 4.26
CHEMBL141530 ECHINATIN 1 4.24
CHEMBL2382114 1 4.12
CHEMBL2382112 1 4.02
CHEMBL2382054 1 -
CHEMBL2382055 1 -
CHEMBL2382056 1 -
CHEMBL2382057 1 -
CHEMBL2382058 1 -
CHEMBL2382059 1 -
CHEMBL2382115 1 -
CHEMBL8102 1 -
CHEMBL1928752 1 -
CHEMBL2148111 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2368566 IC50 = 65.6 nM 7.18
CHEMBL2382116 IC50 = 1810.0 nM 5.74
CHEMBL2382117 IC50 = 28670.0 nM 4.54
CHEMBL2382119 IC50 = 28950.0 nM 4.54
CHEMBL2382113 IC50 = 46810.0 nM 4.33
CHEMBL2382118 IC50 = 54290.0 nM 4.26
CHEMBL141530 ECHINATIN IC50 = 57680.0 nM 4.24
CHEMBL2382114 IC50 = 76470.0 nM 4.12
CHEMBL2382112 IC50 = 95090.0 nM 4.02
CHEMBL2382054 IC50 > 100000.0 nM -
CHEMBL2382055 IC50 > 100000.0 nM -
CHEMBL2382056 IC50 > 100000.0 nM -
CHEMBL2382057 IC50 > 100000.0 nM -
CHEMBL2382058 IC50 > 100000.0 nM -
CHEMBL2382059 IC50 > 100000.0 nM -
CHEMBL2382115 IC50 > 100000.0 nM -
CHEMBL8102 IC50 > 100000.0 nM -
CHEMBL1928752 IC50 > 100000.0 nM -
CHEMBL2148111 IC50 > 100000.0 nM -