Reaction Details |
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Target | Bifunctional epoxide hydrolase 2 |
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Ligand | BDBM50445752 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1284567 (CHEMBL3106762) |
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IC50 | 28±n/a nM |
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Citation | Kato, Y; Fuchi, N; Nishimura, Y; Watanabe, A; Yagi, M; Nakadera, Y; Higashi, E; Yamada, M; Aoki, T; Kigoshi, H Discovery of 1-oxa-4,9-diazaspiro[5.5]undecane-based trisubstituted urea derivatives as highly potent soluble epoxide hydrolase inhibitors and orally active drug candidates for treating of chronic kidney diseases. Bioorg Med Chem Lett24:565-70 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Bifunctional epoxide hydrolase 2 |
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Name: | Bifunctional epoxide hydrolase 2 |
Synonyms: | Ephx2 | Epoxide hydrolase 2 | HYES_RAT |
Type: | PROTEIN |
Mol. Mass.: | 62337.15 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_1465995 |
Residue: | 554 |
Sequence: | MALRVAAFDLDGVLALPSIAGVLRHTEEALALPRDFLLGAFQMKFPEGPTEQLMKGKITF
SQWVPLMDESCRKSSKACGASLPENFSISEIFSQAMAARSINRPMLQAAAALKKKGFTTC
IVTNNWLDDSDKRDILAQMMCELSQHFDFLIESCQVGMIKPEPQIYKFVLDTLKAKPNEV
VFLDDFGSNLKPARDMGMVTILVRDTASALRELEKVTGTQFPEAPLPVPCSPNDVSHGYV
TVKPGIRLHFVEMGSGPAICLCHGFPESWFSWRYQIPALAQAGFRVLAIDMKGYGDSSSP
PEIEEYAMELLCEEMVTFLNKLGIPQAVFIGHDWAGVLVWNMALFHPERVRAVASLNTPL
MPPNPEVSPMEVIRSIPVFNYQLYFQEPGVAEAELEKNMSRTFKSFFRTSDDMGLLTVNK
ATEMGGILVGTPEDPKVSKITTEEEIEYYIQQFKKSGFRGPLNWYRNTERNWKWSCKALG
RKILVPALMVTAEKDIVLRPEMSKNMENWIPFLKRGHIEDCGHWTQIEKPAEVNQILIKW
LKTEIQNPSVTSKI
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BDBM50445752 |
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n/a |
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Name | BDBM50445752 |
Synonyms: | CHEMBL3104441 |
Type | Small organic molecule |
Emp. Form. | C26H28F3N3O4 |
Mol. Mass. | 503.5134 |
SMILES | FC(F)(F)Oc1ccc(NC(=O)N2CCOC3(CCN(CC3)C(=O)C3(CC3)c3ccccc3)C2)cc1 |
Structure |
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