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Assay Detail

CHEMBL3887059

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

Binding
Cell Free Inhibition Assay: The inhibitory concentrations (IC50, [uM]) of the beta -lactamase inhibitors against purified TEM-1, SHV-1 and AmpC beta -lactamases are assessed by determining the concentration of inhibitor at which 50% of the nitrocefin hydrolysis is inhibited by the particular enzyme. Assays are performed with beta -lactamases expressed in the pET system (Novagen, San Diego, Calif.) without signal peptides. They contain an N-terminal hexa-Histidine tag that is used for purification on Ni-NTA (Qiagen, Hilden, Germany). The compounds are prepared as 50 mM stocks in DMSO and diluted into buffer P1 (50 mM phosphate, pH 7) to a final concentration of 10% DMSO. All further dilutions are done in P2 (P1 with 10% DMSO). Enzyme and compound dilutions are pre-incubated for 10 min at 37 C. and the reaction is started with the addition of pre-warmed (37 C.) nitrocefin at a final concentration of 50 mM. The change in absorption at 490 nm is followed at 37 C. for 10 min with 30 s intervals.
51
Total Activities
42
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Beta-lactamase TEM (CHEMBL2364670)
Type SINGLE PROTEIN
Organism Bacteria

Publication

Substituted clavulanic acid
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 51 6.70 9.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4114803 2 9.70
CHEMBL4111477 2 9.40
CHEMBL4114749 1 8.85
CHEMBL4106598 1 8.74
CHEMBL4106976 1 8.62
CHEMBL4109897 1 8.46
CHEMBL4114669 1 8.38
CHEMBL4114818 1 8.04
CHEMBL4114672 1 7.97
CHEMBL404 TAZOBACTAM 4.0 1 7.76
CHEMBL4114697 1 7.66
CHEMBL4115687 1 7.57
CHEMBL777 CLAVULANIC ACID 4.0 1 7.53
CHEMBL4114754 1 7.51
CHEMBL4114694 1 7.36
CHEMBL4114788 1 7.19
CHEMBL4114663 1 7.18
CHEMBL4114696 1 7.14
CHEMBL4114757 1 7.11
CHEMBL4114713 1 7.05
CHEMBL4114769 1 7.01
CHEMBL4114759 1 6.92
CHEMBL4114790 1 6.85
CHEMBL4114761 1 6.59
CHEMBL4114792 2 6.39
CHEMBL4114763 2 6.37
CHEMBL3949733 1 6.19
CHEMBL4114673 2 6.08
CHEMBL3964842 1 6.06
CHEMBL4114809 1 6.02

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4114803 IC50 = 0.2 nM 9.70
CHEMBL4111477 IC50 = 0.4 nM 9.40
CHEMBL4114749 IC50 = 1.4 nM 8.85
CHEMBL4111477 IC50 = 1.7 nM 8.77
CHEMBL4114803 IC50 = 1.7 nM 8.77
CHEMBL4106598 IC50 = 1.8 nM 8.74
CHEMBL4106976 IC50 = 2.4 nM 8.62
CHEMBL4109897 IC50 = 3.5 nM 8.46
CHEMBL4114669 IC50 = 4.2 nM 8.38
CHEMBL4114818 IC50 = 9.2 nM 8.04
CHEMBL4114672 IC50 = 10.6 nM 7.97
CHEMBL404 TAZOBACTAM IC50 = 17.2 nM 7.76
CHEMBL4114697 IC50 = 21.7 nM 7.66
CHEMBL4115687 IC50 = 27.1 nM 7.57
CHEMBL777 CLAVULANIC ACID IC50 = 29.5 nM 7.53
CHEMBL4114754 IC50 = 30.6 nM 7.51
CHEMBL4114694 IC50 = 44.2 nM 7.36
CHEMBL4114788 IC50 = 65.2 nM 7.19
CHEMBL4114663 IC50 = 66.6 nM 7.18
CHEMBL4114696 IC50 = 72.8 nM 7.14
CHEMBL4114757 IC50 = 78.4 nM 7.11
CHEMBL4114713 IC50 = 89.0 nM 7.05
CHEMBL4114769 IC50 = 97.0 nM 7.01
CHEMBL4114759 IC50 = 121.5 nM 6.92
CHEMBL4114790 IC50 = 139.9 nM 6.85
CHEMBL4114761 IC50 = 254.0 nM 6.59
CHEMBL4114792 IC50 = 407.6 nM 6.39
CHEMBL4114763 IC50 = 426.1 nM 6.37
CHEMBL3949733 IC50 = 639.4 nM 6.19
CHEMBL4114673 IC50 = 827.5 nM 6.08
CHEMBL3964842 IC50 = 870.6 nM 6.06
CHEMBL4114809 IC50 = 945.4 nM 6.02
CHEMBL403 SULBACTAM IC50 = 1065.9 nM 5.97
CHEMBL4114792 IC50 = 1561.5 nM 5.81
CHEMBL4115678 IC50 = 1948.6 nM 5.71
CHEMBL3917939 IC50 = 2792.3 nM 5.55
CHEMBL4115684 IC50 = 4124.9 nM 5.38
CHEMBL4114662 IC50 = 4268.3 nM 5.37
CHEMBL4114687 IC50 = 4392.3 nM 5.36
CHEMBL3917939 IC50 = 4923.3 nM 5.31
CHEMBL4114673 IC50 = 5642.2 nM 5.25
CHEMBL4114806 IC50 = 5897.7 nM 5.23
CHEMBL4114806 IC50 = 7306.7 nM 5.14
CHEMBL4115678 IC50 = 8016.0 nM 5.10
CHEMBL4114670 IC50 = 8386.3 nM 5.08
CHEMBL4114791 IC50 = 13259.6 nM 4.88
CHEMBL4114789 IC50 = 17789.0 nM 4.75
CHEMBL4114662 IC50 = 19632.0 nM 4.71
CHEMBL4114780 IC50 = 23621.5 nM 4.63
CHEMBL4114763 IC50 = 45684.4 nM 4.34