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Assay Detail

CHEMBL3887295

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

Binding
Biochemical Assay: A solution of test compound was added to a diluted microsome preparation containing human mPGES-1 and pre-incubated for 15 minutes in potassium phosphate buffer pH 6.8 with cofactor glutathione (GSH). Corresponding solutions without test compound were used as positive controls, and corresponding solutions without test compound and without microsomes were used as negative controls. The enzymatic reaction was then started by addition of the substrate PGH2 in an organic solution (dry acetonitrile).The typical reaction conditions of the enzymatic reaction were thus: Test compound: ranging from 60 uM to 0.002 uM, or zero in positive and negative controls; potassium phosphate buffer pH 6.8: 50 mM; GSH: 2.5 mM; mPGES-1-containing microsomes: 2 ug/mL (sample and positive controls) or 0 ug/mL (negative control); PGH2: 10.8 uM; Acetonitrile: 7.7% (v/v); DMSO: 0.6% (v/v). The reaction was stopped after one minute by adding an acidic solution (pH 1.9) of ferric chloride.
240
Total Activities
239
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Prostaglandin E synthase 2 (CHEMBL4411)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Bis-(sulfonylamino) derivatives for use in therapy
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 240 5.99 7.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3962955 1 7.66
CHEMBL3986331 1 7.51
CHEMBL3904203 1 7.44
CHEMBL3897379 1 7.40
CHEMBL3961959 1 7.39
CHEMBL3943504 1 7.36
CHEMBL3943346 1 7.26
CHEMBL3965498 1 7.24
CHEMBL3968523 1 7.13
CHEMBL3966442 1 7.13
CHEMBL3930981 1 7.12
CHEMBL3942994 1 7.11
CHEMBL3898952 1 7.10
CHEMBL3935976 1 7.09
CHEMBL3951095 1 7.08
CHEMBL3957120 1 7.04
CHEMBL3918947 1 7.01
CHEMBL3946465 1 7.00
CHEMBL3908925 1 6.96
CHEMBL3941676 1 6.96
CHEMBL3889985 1 6.92
CHEMBL3959989 1 6.89
CHEMBL3907650 1 6.89
CHEMBL3975393 1 6.89
CHEMBL3903992 1 6.89
CHEMBL3951825 1 6.89
CHEMBL3906349 1 6.85
CHEMBL3943912 1 6.85
CHEMBL3911159 1 6.82
CHEMBL3960265 1 6.80

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3962955 IC50 = 22.0 nM 7.66
CHEMBL3986331 IC50 = 31.0 nM 7.51
CHEMBL3904203 IC50 = 36.0 nM 7.44
CHEMBL3897379 IC50 = 40.0 nM 7.40
CHEMBL3961959 IC50 = 41.0 nM 7.39
CHEMBL3943504 IC50 = 44.0 nM 7.36
CHEMBL3943346 IC50 = 55.0 nM 7.26
CHEMBL3965498 IC50 = 57.0 nM 7.24
CHEMBL3968523 IC50 = 74.0 nM 7.13
CHEMBL3966442 IC50 = 74.0 nM 7.13
CHEMBL3930981 IC50 = 75.0 nM 7.12
CHEMBL3942994 IC50 = 77.0 nM 7.11
CHEMBL3898952 IC50 = 79.0 nM 7.10
CHEMBL3935976 IC50 = 81.0 nM 7.09
CHEMBL3951095 IC50 = 84.0 nM 7.08
CHEMBL3957120 IC50 = 91.0 nM 7.04
CHEMBL3918947 IC50 = 97.0 nM 7.01
CHEMBL3946465 IC50 = 100.0 nM 7.00
CHEMBL3941676 IC50 = 110.0 nM 6.96
CHEMBL3908925 IC50 = 110.0 nM 6.96
CHEMBL3889985 IC50 = 120.0 nM 6.92
CHEMBL3907650 IC50 = 130.0 nM 6.89
CHEMBL3959989 IC50 = 130.0 nM 6.89
CHEMBL3903992 IC50 = 130.0 nM 6.89
CHEMBL3951825 IC50 = 130.0 nM 6.89
CHEMBL3975393 IC50 = 130.0 nM 6.89
CHEMBL3906349 IC50 = 140.0 nM 6.85
CHEMBL3943912 IC50 = 140.0 nM 6.85
CHEMBL3911159 IC50 = 150.0 nM 6.82
CHEMBL3891144 IC50 = 160.0 nM 6.80
CHEMBL3960265 IC50 = 160.0 nM 6.80
CHEMBL3960306 IC50 = 170.0 nM 6.77
CHEMBL3913683 IC50 = 180.0 nM 6.75
CHEMBL3968505 IC50 = 190.0 nM 6.72
CHEMBL3923779 IC50 = 190.0 nM 6.72
CHEMBL3928194 IC50 = 190.0 nM 6.72
CHEMBL3911878 IC50 = 220.0 nM 6.66
CHEMBL3977611 IC50 = 220.0 nM 6.66
CHEMBL3926649 IC50 = 220.0 nM 6.66
CHEMBL3932675 IC50 = 220.0 nM 6.66
CHEMBL3906406 IC50 = 220.0 nM 6.66
CHEMBL3958446 IC50 = 250.0 nM 6.60
CHEMBL3958405 IC50 = 270.0 nM 6.57
CHEMBL3957650 IC50 = 270.0 nM 6.57
CHEMBL3926208 IC50 = 270.0 nM 6.57
CHEMBL3919221 IC50 = 270.0 nM 6.57
CHEMBL3961503 IC50 = 270.0 nM 6.57
CHEMBL3948341 IC50 = 270.0 nM 6.57
CHEMBL3956630 IC50 = 270.0 nM 6.57
CHEMBL3957007 IC50 = 280.0 nM 6.55