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Assay Detail

CHEMBL3887909

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

Binding
TGM2 Inhibitory Activity Assay: 2 ul of a solution of different concentrations of the test compound in dimethyl sulfoxide was added to 28 ul of buffer (50 mM TRIS, 100 mM NaCl, 10 mM CaCl2, pH 7.5) and 10 ul of a TGM2 solution to give a TMG2 test concentration of 25 ug/ml, and the mixture incubated for 15 minutes at room temperature in a 96 half-well microtiter plate. The enzyme reaction was started by the addition of 10 ul of substrate solution containing H-Abz-APE(CAD-DNP)QEA-OH and glycine methyl ester hydrochloride in buffer to give test concentrations of H-Abz-APE(CAD-DNP)QEA-OH of 50 uM and of glycine methyl ester hydrochloride of 5 mM. The time course of the reaction was monitored with excitation at 318 nm and measurement at emission wavelength 418 nm in a microtiter plate reader (SpectraMax M5, Molecular Devices) over 15 minutes. Rates were calculated from the linear part of the curve (generally between 5 and 10 minutes). IC50 values were calculated from the means (duplicates) of a dilution series of the com
41
Total Activities
40
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Protein-glutamine gamma-glutamyltransferase (CHEMBL2730)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Isothiazolopyridine-2-carboxamides and their use as pharmaceuticals
(2016)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 41 6.32 7.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3949090 1 7.85
CHEMBL3968388 1 7.35
CHEMBL3932512 1 7.27
CHEMBL3901025 1 7.21
CHEMBL3891796 1 7.21
CHEMBL3900780 1 7.21
CHEMBL3927771 1 7.19
CHEMBL3923158 1 7.14
CHEMBL3977367 1 6.96
CHEMBL3969704 1 6.92
CHEMBL3966197 1 6.92
CHEMBL3895571 1 6.89
CHEMBL3977893 1 6.85
CHEMBL3894353 1 6.82
CHEMBL3900394 2 6.70
CHEMBL3977899 1 6.62
CHEMBL3943876 1 6.60
CHEMBL3901279 1 6.57
CHEMBL3976921 1 6.47
CHEMBL3952109 1 6.47
CHEMBL3915197 1 6.43
CHEMBL3906227 1 6.38
CHEMBL3960810 1 6.37
CHEMBL3915022 1 6.12
CHEMBL3897091 1 6.10
CHEMBL3927276 1 6.00
CHEMBL3924708 1 5.96
CHEMBL3923568 1 5.92
CHEMBL4106615 1 5.85
CHEMBL3921879 1 5.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3949090 IC50 = 14.0 nM 7.85
CHEMBL3968388 IC50 = 45.0 nM 7.35
CHEMBL3932512 IC50 = 54.0 nM 7.27
CHEMBL3901025 IC50 = 62.0 nM 7.21
CHEMBL3891796 IC50 = 61.0 nM 7.21
CHEMBL3900780 IC50 = 62.0 nM 7.21
CHEMBL3927771 IC50 = 65.0 nM 7.19
CHEMBL3923158 IC50 = 72.0 nM 7.14
CHEMBL3977367 IC50 = 110.0 nM 6.96
CHEMBL3969704 IC50 = 120.0 nM 6.92
CHEMBL3966197 IC50 = 120.0 nM 6.92
CHEMBL3895571 IC50 = 130.0 nM 6.89
CHEMBL3977893 IC50 = 140.0 nM 6.85
CHEMBL3894353 IC50 = 150.0 nM 6.82
CHEMBL3900394 IC50 = 200.0 nM 6.70
CHEMBL3977899 IC50 = 240.0 nM 6.62
CHEMBL3943876 IC50 = 250.0 nM 6.60
CHEMBL3901279 IC50 = 270.0 nM 6.57
CHEMBL3976921 IC50 = 340.0 nM 6.47
CHEMBL3952109 IC50 = 340.0 nM 6.47
CHEMBL3915197 IC50 = 370.0 nM 6.43
CHEMBL3906227 IC50 = 420.0 nM 6.38
CHEMBL3960810 IC50 = 430.0 nM 6.37
CHEMBL3915022 IC50 = 750.0 nM 6.12
CHEMBL3897091 IC50 = 800.0 nM 6.10
CHEMBL3927276 IC50 = 1000.0 nM 6.00
CHEMBL3924708 IC50 = 1100.0 nM 5.96
CHEMBL3923568 IC50 = 1200.0 nM 5.92
CHEMBL4106615 IC50 = 1400.0 nM 5.85
CHEMBL3921879 IC50 = 1700.0 nM 5.77
CHEMBL3907791 IC50 = 1700.0 nM 5.77
CHEMBL3949657 IC50 = 2000.0 nM 5.70
CHEMBL3901759 IC50 = 2100.0 nM 5.68
CHEMBL3903786 IC50 = 2300.0 nM 5.64
CHEMBL3900394 IC50 = 2600.0 nM 5.58
CHEMBL3938009 IC50 = 2900.0 nM 5.54
CHEMBL3987140 IC50 = 3100.0 nM 5.51
CHEMBL3894858 IC50 = 4300.0 nM 5.37
CHEMBL3972400 IC50 = 12000.0 nM 4.92
CHEMBL3953534 IC50 = 18000.0 nM 4.75
CHEMBL3916611 IC50 = 26000.0 nM 4.58