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Assay Detail

CHEMBL2318866

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

Binding
Inhibition of human sEH assessed as 6-methoxy-2-naphthaldehyde generation preincubated for 10 before addition of cyano(2-methyl-oxynaphthalen-6-yl)methyl trans-(3-phenyloxyran-2-yl) methyl carbonate by fluorescence analysis
46
Total Activities
46
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Bifunctional epoxide hydrolase 2 (CHEMBL2409)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and structure-activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors.
Pecic S, Pakhomova S, Newcomer ME, Morisseau C, Hammock BD, Zhu Z, Rinderspacher A, Deng SX.
Bioorg Med Chem Lett (2013) 23 : 417 -421
PubMed 23237835 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 46 7.70 9.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2313193 1 9.40
CHEMBL2313183 1 9.22
CHEMBL2313191 1 9.22
CHEMBL2313190 1 8.96
CHEMBL2313192 1 8.92
CHEMBL2313176 1 8.80
CHEMBL2313189 1 8.77
CHEMBL2313181 1 8.64
CHEMBL2313166 1 8.55
CHEMBL2313162 1 8.34
CHEMBL2313161 1 8.28
CHEMBL2313186 1 8.28
CHEMBL2313188 1 8.24
CHEMBL2313203 1 8.22
CHEMBL2313175 1 8.17
CHEMBL2313167 1 8.16
CHEMBL2313180 1 8.08
CHEMBL2313194 1 8.07
CHEMBL2313168 1 8.06
CHEMBL2313173 1 7.92
CHEMBL2313159 1 7.89
CHEMBL2313172 1 7.77
CHEMBL2313204 1 7.75
CHEMBL2313169 1 7.70
CHEMBL2313171 1 7.70
CHEMBL2313196 1 7.70
CHEMBL2313195 1 7.64
CHEMBL2313182 1 7.64
CHEMBL2313201 1 7.60
CHEMBL2313170 1 7.60

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2313193 IC50 = 0.4 nM 9.40
CHEMBL2313183 IC50 = 0.6 nM 9.22
CHEMBL2313191 IC50 = 0.6 nM 9.22
CHEMBL2313190 IC50 = 1.1 nM 8.96
CHEMBL2313192 IC50 = 1.2 nM 8.92
CHEMBL2313176 IC50 = 1.6 nM 8.80
CHEMBL2313189 IC50 = 1.7 nM 8.77
CHEMBL2313181 IC50 = 2.3 nM 8.64
CHEMBL2313166 IC50 = 2.8 nM 8.55
CHEMBL2313162 IC50 = 4.6 nM 8.34
CHEMBL2313161 IC50 = 5.2 nM 8.28
CHEMBL2313186 IC50 = 5.2 nM 8.28
CHEMBL2313188 IC50 = 5.8 nM 8.24
CHEMBL2313203 IC50 = 6.0 nM 8.22
CHEMBL2313175 IC50 = 6.7 nM 8.17
CHEMBL2313167 IC50 = 6.9 nM 8.16
CHEMBL2313180 IC50 = 8.3 nM 8.08
CHEMBL2313194 IC50 = 8.5 nM 8.07
CHEMBL2313168 IC50 = 8.7 nM 8.06
CHEMBL2313173 IC50 = 12.0 nM 7.92
CHEMBL2313159 IC50 = 13.0 nM 7.89
CHEMBL2313172 IC50 = 17.0 nM 7.77
CHEMBL2313204 IC50 = 18.0 nM 7.75
CHEMBL2313169 IC50 = 20.0 nM 7.70
CHEMBL2313196 IC50 = 20.0 nM 7.70
CHEMBL2313171 IC50 = 20.0 nM 7.70
CHEMBL2313195 IC50 = 23.0 nM 7.64
CHEMBL2313182 IC50 = 23.0 nM 7.64
CHEMBL2313201 IC50 = 25.0 nM 7.60
CHEMBL2313170 IC50 = 25.0 nM 7.60
CHEMBL2313163 IC50 = 29.0 nM 7.54
CHEMBL2313198 IC50 = 30.0 nM 7.52
CHEMBL2313165 IC50 = 41.0 nM 7.39
CHEMBL2313174 IC50 = 43.0 nM 7.37
CHEMBL2313178 IC50 = 45.0 nM 7.35
CHEMBL2313202 IC50 = 55.0 nM 7.26
CHEMBL2313179 IC50 = 78.0 nM 7.11
CHEMBL2313164 IC50 = 102.0 nM 6.99
CHEMBL2313160 IC50 = 110.0 nM 6.96
CHEMBL2313197 IC50 = 250.0 nM 6.60
CHEMBL2313187 IC50 = 263.0 nM 6.58
CHEMBL2313177 IC50 = 290.0 nM 6.54
CHEMBL2313199 IC50 = 640.0 nM 6.19
CHEMBL2313200 IC50 = 2200.0 nM 5.66
CHEMBL2313185 IC50 = 6900.0 nM 5.16
CHEMBL2313184 IC50 = 30000.0 nM 4.52