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Assay Detail

CHEMBL5734342

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

Binding
Biological Evaluation: The relative efficacies of Formula I compounds as inhibitors of an enzyme activity (or other biological activity) can be established by determining the concentrations at which each compound inhibits the activity to a predefined extent and then comparing the results. Typically, the preferred determination is the concentration that inhibits 50% of the activity in a biochemical assay, i.e., the 50% inhibitory concentration or “IC50”. Determination of IC50 values can be accomplished using conventional techniques known in the art. In general, an IC50 can be determined by measuring the activity of a given enzyme in the presence of a range of concentrations of the inhibitor under study. The experimentally obtained values of enzyme activity then are plotted against the inhibitor concentrations used. The concentration of the inhibitor that shows 50% enzyme activity (as compared to the activity in the absence of any inhibitor) is taken as the IC50 value. Analogously, other inhibitory concentrations can be defined through appropriate determinations of activity.
120
Total Activities
40
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

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

Target

Estrogen receptor (CHEMBL206)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Tetrahydronaphthalene estrogen receptor modulators and uses thereof
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 40 8.75 10.54
kon 40 - -
k_off 40 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5787193 3 10.54
CHEMBL5756797 3 10.44
CHEMBL5959890 3 10.43
CHEMBL5948183 3 10.42
CHEMBL5869147 3 10.40
CHEMBL5822315 3 10.34
CHEMBL5820677 3 10.00
CHEMBL5829864 3 9.97
CHEMBL5847295 3 9.79
CHEMBL5990094 3 9.75
CHEMBL5809491 3 9.75
CHEMBL5827282 3 9.73
CHEMBL6059949 3 9.69
CHEMBL5757221 3 9.68
CHEMBL5972367 3 9.64
CHEMBL5962014 3 9.43
CHEMBL5974609 3 9.35
CHEMBL5942493 3 9.17
CHEMBL5858899 3 9.11
CHEMBL5877418 3 9.01
CHEMBL6037613 3 8.09
CHEMBL6049754 3 7.90
CHEMBL6064787 3 7.86
CHEMBL6011128 3 7.84
CHEMBL5754083 3 7.81
CHEMBL6057223 3 7.79
CHEMBL5937863 3 7.78
CHEMBL5859562 3 7.77
CHEMBL5870590 3 7.53
CHEMBL5880673 3 7.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5787193 EC50 = 0.029 nM 10.54
CHEMBL5756797 EC50 = 0.036 nM 10.44
CHEMBL5959890 EC50 = 0.037 nM 10.43
CHEMBL5948183 EC50 = 0.038 nM 10.42
CHEMBL5869147 EC50 = 0.04 nM 10.40
CHEMBL5822315 EC50 = 0.046 nM 10.34
CHEMBL5820677 EC50 = 0.1 nM 10.00
CHEMBL5829864 EC50 = 0.107 nM 9.97
CHEMBL5847295 EC50 = 0.164 nM 9.79
CHEMBL5990094 EC50 = 0.177 nM 9.75
CHEMBL5809491 EC50 = 0.177 nM 9.75
CHEMBL5827282 EC50 = 0.184 nM 9.73
CHEMBL6059949 EC50 = 0.203 nM 9.69
CHEMBL5757221 EC50 = 0.208 nM 9.68
CHEMBL5972367 EC50 = 0.227 nM 9.64
CHEMBL5962014 EC50 = 0.371 nM 9.43
CHEMBL5974609 EC50 = 0.451 nM 9.35
CHEMBL5942493 EC50 = 0.675 nM 9.17
CHEMBL5858899 EC50 = 0.773 nM 9.11
CHEMBL5877418 EC50 = 0.977 nM 9.01
CHEMBL6037613 EC50 = 8.12 nM 8.09
CHEMBL6049754 EC50 = 12.5 nM 7.90
CHEMBL6064787 EC50 = 13.8 nM 7.86
CHEMBL6011128 EC50 = 14.6 nM 7.84
CHEMBL5754083 EC50 = 15.6 nM 7.81
CHEMBL6057223 EC50 = 16.4 nM 7.79
CHEMBL5937863 EC50 = 16.5 nM 7.78
CHEMBL5859562 EC50 = 16.9 nM 7.77
CHEMBL5870590 EC50 = 29.8 nM 7.53
CHEMBL5856363 EC50 = 38.6 nM 7.41
CHEMBL5880673 EC50 = 39.4 nM 7.41
CHEMBL5774872 EC50 = 47.0 nM 7.33
CHEMBL5894884 EC50 = 50.9 nM 7.29
CHEMBL5778441 EC50 = 53.0 nM 7.28
CHEMBL5856995 EC50 = 186.0 nM 6.73
CHEMBL5790936 EC50 = 186.0 nM 6.73
CHEMBL5859872 EC50 = 228.0 nM 6.64
CHEMBL5942493 kon = - -
CHEMBL5774204 k_off = - s-1 -
CHEMBL5774204 kon = - -
CHEMBL5858899 kon = - -
CHEMBL5774204 EC50 > 100.0 nM -
CHEMBL5859872 k_off = - s-1 -
CHEMBL6059949 kon = - -
CHEMBL5822315 kon = - -
CHEMBL5822315 k_off = - s-1 -
CHEMBL5856995 k_off = - s-1 -
CHEMBL5856995 kon = - -
CHEMBL6049754 kon = - -
CHEMBL5942493 k_off = - s-1 -