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Assay Detail

CHEMBL899137

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Binding
Inhibition of human recombinant caspase 3 by fluorometric assay
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Caspase-3 (CHEMBL2334)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: peptidomimetic replacement of the P(2) amino acid by 2-aminoaryl acids and other non-natural amino acids.
Wang Y, Jia S, Tseng B, Drewe J, Cai SX.
Bioorg Med Chem Lett (2007) 17 : 6178 -6182
PubMed 17889532 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 6.44 7.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL237310 1 7.48
CHEMBL237308 1 7.00
CHEMBL237088 1 7.00
CHEMBL391494 1 6.70
CHEMBL429632 1 6.68
CHEMBL391709 1 6.60
CHEMBL236465 1 6.58
CHEMBL391708 1 6.57
CHEMBL391511 1 6.50
CHEMBL237309 1 6.47
CHEMBL393200 1 6.39
CHEMBL236667 1 6.35
CHEMBL236879 1 6.26
CHEMBL391495 1 6.14
CHEMBL236464 1 6.07
CHEMBL236666 1 5.77
CHEMBL393199 1 5.72
CHEMBL236880 1 5.60

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL237310 IC50 = 33.0 nM 7.48
CHEMBL237308 IC50 = 100.0 nM 7.00
CHEMBL237088 IC50 = 100.0 nM 7.00
CHEMBL391494 IC50 = 200.0 nM 6.70
CHEMBL429632 IC50 = 210.0 nM 6.68
CHEMBL391709 IC50 = 250.0 nM 6.60
CHEMBL236465 IC50 = 260.0 nM 6.58
CHEMBL391708 IC50 = 270.0 nM 6.57
CHEMBL391511 IC50 = 320.0 nM 6.50
CHEMBL237309 IC50 = 340.0 nM 6.47
CHEMBL393200 IC50 = 410.0 nM 6.39
CHEMBL236667 IC50 = 450.0 nM 6.35
CHEMBL236879 IC50 = 550.0 nM 6.26
CHEMBL391495 IC50 = 720.0 nM 6.14
CHEMBL236464 IC50 = 860.0 nM 6.07
CHEMBL236666 IC50 = 1700.0 nM 5.77
CHEMBL393199 IC50 = 1900.0 nM 5.72
CHEMBL236880 IC50 = 2500.0 nM 5.60