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Assay Detail

CHEMBL5731993

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

Binding
In Vitro Inhibitory Activity of Caspase: Selectivity of compound 55, compound 63, compound 48, compound 57, compound 88 toward caspase-1 (pro-inflammatory group), caspase-5 (group I), caspase-9 (group II) and caspase-3 and caspase-7 (group III) was evaluated by using fluorometric methods using the Caspase-1, -3, -5, -7, -9 Inhibitor Drug Screening Kit (Catalog #: K151-100, K153-100, K155-100, K157-100, K159-100 respectively, BioVision). Briefly, using instructions of the manufacturer, a wide range of different concentrations of the compound: 3333, 1000, 333, 100, 33, 10, 3, and 1 nM (final concentration) was added directly to the reaction mixtures containing the substrate and the enzyme in a final volume of 10 μl After a 30-minute incubation at 37° C., the liberation of AFC was measured as an endpoint assay using the Flexstation3 (Molecular Devices) with an excitation wavelength of 400 nm and an emission wavelength of 505 nm. The level of inhibition of caspase-1, -3, -5, -7, -9 activity was determined by comparison of the relative fluorescence intensity in samples with or without the compound.
81
Total Activities
25
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Selective caspase inhibitors and uses thereof
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 27 7.21 8.00
kon 27 - -
k_off 27 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3673267 3 8.00
CHEMBL3673259 9 8.00
CHEMBL3673263 3 8.00
CHEMBL3673265 3 7.70
CHEMBL3673264 3 7.52
CHEMBL3678066 3 7.52
CHEMBL3678068 3 7.52
CHEMBL3678069 3 7.40
CHEMBL3673266 3 7.40
CHEMBL3673262 3 7.22
CHEMBL3673270 3 7.00
CHEMBL5774008 3 7.00
CHEMBL3673269 3 6.70
CHEMBL3673268 3 6.70
CHEMBL5898984 3 6.52
CHEMBL3678067 3 6.52
CHEMBL3673261 3 6.00
CHEMBL3673256 3 -
CHEMBL3678070 3 -
CHEMBL3673255 3 -
CHEMBL3673258 3 -
CHEMBL1242699 3 -
CHEMBL3673257 3 -
CHEMBL3678071 3 -
CHEMBL3673260 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3673267 IC50 = 10.0 nM 8.00
CHEMBL3673259 IC50 = 10.0 nM 8.00
CHEMBL3673259 IC50 = 10.0 nM 8.00
CHEMBL3673263 IC50 = 10.0 nM 8.00
CHEMBL3673265 IC50 = 20.0 nM 7.70
CHEMBL3678068 IC50 = 30.0 nM 7.52
CHEMBL3678066 IC50 = 30.0 nM 7.52
CHEMBL3673264 IC50 = 30.0 nM 7.52
CHEMBL3673266 IC50 = 40.0 nM 7.40
CHEMBL3678069 IC50 = 40.0 nM 7.40
CHEMBL3673262 IC50 = 60.0 nM 7.22
CHEMBL3673270 IC50 = 100.0 nM 7.00
CHEMBL5774008 IC50 = 100.0 nM 7.00
CHEMBL3673268 IC50 = 200.0 nM 6.70
CHEMBL3673269 IC50 = 200.0 nM 6.70
CHEMBL3678067 IC50 = 300.0 nM 6.52
CHEMBL5898984 IC50 = 300.0 nM 6.52
CHEMBL3673259 IC50 = 600.0 nM 6.22
CHEMBL3673261 IC50 = 1000.0 nM 6.00
CHEMBL3673261 kon = - -
CHEMBL3673261 k_off = - s-1 -
CHEMBL3673262 kon = - -
CHEMBL3673258 IC50 > 2000.0 nM -
CHEMBL1242699 kon = - -
CHEMBL1242699 IC50 > 3330.0 nM -
CHEMBL3673265 k_off = - s-1 -
CHEMBL3673265 kon = - -
CHEMBL3678067 k_off = - s-1 -
CHEMBL3678069 k_off = - s-1 -
CHEMBL3678069 kon = - -
CHEMBL3673269 kon = - -
CHEMBL3673269 k_off = - s-1 -
CHEMBL3673264 k_off = - s-1 -
CHEMBL3673264 kon = - -
CHEMBL3673259 kon = - -
CHEMBL3673259 k_off = - s-1 -
CHEMBL3678066 k_off = - s-1 -
CHEMBL3678066 kon = - -
CHEMBL3673259 kon = - -
CHEMBL3678071 IC50 > 10000.0 nM -
CHEMBL3673270 k_off = - s-1 -
CHEMBL3673270 kon = - -
CHEMBL3678071 kon = - -
CHEMBL3673259 k_off = - s-1 -
CHEMBL3678071 k_off = - s-1 -
CHEMBL3678067 kon = - -
CHEMBL3678068 k_off = - s-1 -
CHEMBL3678068 kon = - -
CHEMBL1242699 k_off = - s-1 -
CHEMBL3673266 kon = - -