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TargetEpoxide hydrolase
LigandBDBM25738
Substrate/Competitorn/a
Meas. Tech.Inhibition Assay
IC50 23.0±n/a nM
Citation Guedes, AGHammock, BDMorisseau, C Treatment of inflammatory disorders in non-human mammals US Patent US10383835 Publication Date 8/20/2019
More Info.:Get all data from this article,  Assay Method
 
Epoxide hydrolase
Name:Epoxide hydrolase
Synonyms:EPHX1
Type:Enzyme
Mol. Mass.:48577.06
Organism:Equus caballus (Horse)
Description:A0A5F5PR84
Residue:462
Sequence:
MMTSLRVMWLEILLTSVLGFVIYWFVSRDKEETLPLEDGWWGPGSRPTGREDESIRPFKV
ETSDEEINDLHQRIDKARLTPPLEDSRFHYGFNSNYLKQIVSYWRNEFDWKKQVEILNRY
PHFKTKIEGLDIHFIHVKPPQLPSGRTPKPLLMVHGWPGSFYEFYKIIPFLTDPKSHGLG
DEHVFEVICPCIPGYGFSEASSKKGFNTVATARIFYKLMLRLGFQEFYVQGGDWGALICT
NIAQLVPSHVKGLHLNMAFVLRSFYTLTLPLGRHFAGLFGYTHKDVELMYPFKEKIFYSL
MRESGYMHIQATKPDTVGCALNDSPVGLAAYILEKFSTWTKSEFRDLEDGGLERKFSLDD
LLTNIMLYWTTGSITSSQRFYKENLGQGYMAHKHERMKVYVPTGFAAFPCELLHAPENWV
KFKYPKLISYSYMPRGGHFAAFEEPQLLAQDIRKFVGLLERQ
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  Blast E-value cutoff:
BDBM25738
n/a
NameBDBM25738
Synonyms:1-adamantan-1-yl-3-{5-[2-(2-ethoxyethoxy)ethoxy]pentyl}urea | CHEMBL242655 | US10383835, Compound 950 | Urea-based compound, 19
TypeSmall organic molecule
Emp. Form.C22H40N2O4
Mol. Mass.396.564
SMILESCCOCCOCCOCCCCCNC(=O)NC12CC3CC(CC(C3)C1)C2 |TLB:25:20:27:24.23.26,25:24:20.21.19:27,THB:23:22:19:24.25.26,23:24:19:22.21.27|
Structure
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