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Assay Detail

CHEMBL5735926

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Binding
Enzymatic Activity Assay of DPP-4: Human DPP-4 ((39-766)-His) and mouse DPP-4 ((29-760)-His) are purified by gel chromatography for use in the assay. The final concentration of hDPP-4 and mDPP-4 in the assay is 0.04 nM and 0.22 nM respectively.Inhibition of the catalytic activity of human and mouse DPP-4 by the compound in the present invention is monitored by the formation of product fluorescence AMC from substrate Gly-Pro-AMC (Sigma, G2761) on an Envision plate reader. The reaction is typically conducted by incubating the enzyme, test compound, and substrate (10 μM) in an assay buffer (75 μl) (0.01% BSA, 0.1 mM EDTA, 50 μM Tris-HCl, 0.01% Triton™-X100, 0.1 M NaCl at pH 7.5) for 30 minutes. After the reaction is stopped by the addition of ZnSO4 (25 μl, 10 mM), the formation of fluorescent product AMC is measured on an Envision plate reader with the excitation wavelength at 355 nm and emission wavelength at 460 nm. The IC50 value is calculated typically from a 10-point dose titration curve using the 4-parameter logistic equation.
51
Total Activities
17
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Mus musculus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Dipeptidyl peptidase 4 (CHEMBL3883)
Type SINGLE PROTEIN
Organism Mus musculus

Publication

Pyrrolidinone compounds
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 8.26 9.32
kon 17 - -
k_off 17 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5859631 3 9.32
CHEMBL5968543 3 9.30
CHEMBL5993878 3 9.25
CHEMBL5914544 3 8.69
CHEMBL6054858 3 8.58
CHEMBL5998893 3 8.45
CHEMBL6000557 3 8.19
CHEMBL5888255 3 8.19
CHEMBL5961410 3 8.11
CHEMBL5858632 3 7.88
CHEMBL5884216 3 7.73
CHEMBL5861052 3 7.59
CHEMBL5903124 3 7.55
CHEMBL5964362 3 7.51
CHEMBL5881243 3 7.49
CHEMBL5818540 3 -
CHEMBL5756218 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5859631 IC50 = 0.474 nM 9.32
CHEMBL5968543 IC50 = 0.498 nM 9.30
CHEMBL5993878 IC50 = 0.564 nM 9.25
CHEMBL5914544 IC50 = 2.03 nM 8.69
CHEMBL6054858 IC50 = 2.64 nM 8.58
CHEMBL5998893 IC50 = 3.57 nM 8.45
CHEMBL5888255 IC50 = 6.53 nM 8.19
CHEMBL6000557 IC50 = 6.46 nM 8.19
CHEMBL5961410 IC50 = 7.73 nM 8.11
CHEMBL5858632 IC50 = 13.1 nM 7.88
CHEMBL5884216 IC50 = 18.6 nM 7.73
CHEMBL5861052 IC50 = 25.5 nM 7.59
CHEMBL5903124 IC50 = 28.3 nM 7.55
CHEMBL5964362 IC50 = 30.7 nM 7.51
CHEMBL5881243 IC50 = 32.5 nM 7.49
CHEMBL6000557 kon = - -
CHEMBL5818540 kon = - -
CHEMBL6000557 k_off = - s-1 -
CHEMBL5881243 kon = - -
CHEMBL5881243 k_off = - s-1 -
CHEMBL5964362 kon = - -
CHEMBL5964362 k_off = - s-1 -
CHEMBL5903124 kon = - -
CHEMBL5903124 k_off = - s-1 -
CHEMBL5756218 IC50 < 1.52 nM -
CHEMBL5859631 k_off = - s-1 -
CHEMBL5968543 kon = - -
CHEMBL5968543 k_off = - s-1 -
CHEMBL5993878 kon = - -
CHEMBL5993878 k_off = - s-1 -
CHEMBL5998893 k_off = - s-1 -
CHEMBL5818540 IC50 < 1.52 nM -
CHEMBL5858632 k_off = - s-1 -
CHEMBL6054858 kon = - -
CHEMBL5756218 kon = - -
CHEMBL6054858 k_off = - s-1 -
CHEMBL5756218 k_off = - s-1 -
CHEMBL5998893 kon = - -
CHEMBL5914544 kon = - -
CHEMBL5914544 k_off = - s-1 -
CHEMBL5858632 kon = - -
CHEMBL5888255 k_off = - s-1 -
CHEMBL5961410 kon = - -
CHEMBL5961410 k_off = - s-1 -
CHEMBL5884216 kon = - -
CHEMBL5884216 k_off = - s-1 -
CHEMBL5861052 kon = - -
CHEMBL5861052 k_off = - s-1 -
CHEMBL5859631 kon = - -
CHEMBL5888255 kon = - -