Reaction Details |
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Target | Epoxide hydrolase 1 |
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Ligand | BDBM50327850 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibition Assay |
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IC50 | 0.4±0.0 nM |
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Citation | Hammock, BD; Jones, PD; Morisseau, C; Huang, H; Tsai, H; Gless, Jr., R Conformationally restricted urea inhibitors of soluble epoxide hydrolase US Patent US8501783 Publication Date 8/6/2013 |
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More Info.: | Get all data from this article, Assay Method |
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Epoxide hydrolase 1 |
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Name: | Epoxide hydrolase 1 |
Synonyms: | EPHX | EPHX1 | EPOX | Epoxide hydrolase (EH) | Epoxide hydrolase (HsEH) | Epoxide hydrolase 1 | HYEP_HUMAN | Microsomal epoxide hydrolase |
Type: | Protein |
Mol. Mass.: | 52954.28 |
Organism: | Homo sapiens (Human) |
Description: | P07099 |
Residue: | 455 |
Sequence: | MWLEILLTSVLGFAIYWFISRDKEETLPLEDGWWGPGTRSAAREDDSIRPFKVETSDEEI
HDLHQRIDKFRFTPPLEDSCFHYGFNSNYLKKVISYWRNEFDWKKQVEILNRYPHFKTKI
EGLDIHFIHVKPPQLPAGHTPKPLLMVHGWPGSFYEFYKIIPLLTDPKNHGLSDEHVFEV
ICPSIPGYGFSEASSKKGFNSVATARIFYKLMLRLGFQEFYIQGGDWGSLICTNMAQLVP
SHVKGLHLNMALVLSNFSTLTLLLGQRFGRFLGLTERDVELLYPVKEKVFYSLMRESGYM
HIQCTKPDTVGSALNDSPVGLAAYILEKFSTWTNTEFRYLEDGGLERKFSLDDLLTNVML
YWTTGTIISSQRFYKENLGQGWMTQKHERMKVYVPTGFSAFPFELLHTPEKWVRFKYPKL
ISYSYMVRGGHFAAFEEPELLAQDIRKFLSVLERQ
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BDBM50327850 |
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n/a |
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Name | BDBM50327850 |
Synonyms: | 1-(1-Tosylpiperidin-4-yl)-3-(4-(trifluoromethoxy)phenyl)urea | CHEMBL1257759 | US8501783, 1711 | US9296693, 58 |
Type | Small organic molecule |
Emp. Form. | C20H22F3N3O4S |
Mol. Mass. | 457.467 |
SMILES | Cc1ccc(cc1)S(=O)(=O)N1CCC(CC1)NC(=O)Nc1ccc(OC(F)(F)F)cc1 |
Structure |
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