Reaction Details |
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Target | Bifunctional epoxide hydrolase 2 |
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Ligand | BDBM50143922 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_67377 (CHEMBL677487) |
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IC50 | 50±n/a nM |
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Citation | Kim, IH; Morisseau, C; Watanabe, T; Hammock, BD Design, synthesis, and biological activity of 1,3-disubstituted ureas as potent inhibitors of the soluble epoxide hydrolase of increased water solubility. J Med Chem47:2110-22 (2004) [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: | Eph2 | Ephx2 | Epoxide hydratase | HYES_MOUSE | Soluble epoxide hydrolase (sEH) |
Type: | Enzyme |
Mol. Mass.: | 62512.06 |
Organism: | Mus musculus (Mouse) |
Description: | P34914 |
Residue: | 554 |
Sequence: | MALRVAAFDLDGVLALPSIAGAFRRSEEALALPRDFLLGAYQTEFPEGPTEQLMKGKITF
SQWVPLMDESYRKSSKACGANLPENFSISQIFSQAMAARSINRPMLQAAIALKKKGFTTC
IVTNNWLDDGDKRDSLAQMMCELSQHFDFLIESCQVGMIKPEPQIYNFLLDTLKAKPNEV
VFLDDFGSNLKPARDMGMVTILVHNTASALRELEKVTGTQFPEAPLPVPCNPNDVSHGYV
TVKPGIRLHFVEMGSGPALCLCHGFPESWFSWRYQIPALAQAGFRVLAIDMKGYGDSSSP
PEIEEYAMELLCKEMVTFLDKLGIPQAVFIGHDWAGVMVWNMALFYPERVRAVASLNTPF
MPPDPDVSPMKVIRSIPVFNYQLYFQEPGVAEAELEKNMSRTFKSFFRASDETGFIAVHK
ATEIGGILVNTPEDPNLSKITTEEEIEFYIQQFKKTGFRGPLNWYRNTERNWKWSCKGLG
RKILVPALMVTAEKDIVLRPEMSKNMEKWIPFLKRGHIEDCGHWTQIEKPTEVNQILIKW
LQTEVQNPSVTSKI
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BDBM50143922 |
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n/a |
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Name | BDBM50143922 |
Synonyms: | 4-(3-Adamantan-1-yl-ureido)-butyric acid 3,7-dimethyl-oct-6-enyl ester | CHEMBL305446 |
Type | Small organic molecule |
Emp. Form. | C25H42N2O3 |
Mol. Mass. | 418.6126 |
SMILES | [#6]-[#6](-[#6]-[#6]-[#8]-[#6](=O)-[#6]-[#6]-[#6]-[#7]-[#6](=O)-[#7]C12[#6]-[#6]-3-[#6]-[#6](-[#6]-[#6](-[#6]-3)-[#6]1)-[#6]2)-[#6]-[#6]\[#6]=[#6](/[#6])-[#6] |THB:19:20:15:18.23.17,19:18:15:20.22.21,22:14:17:20.21.19,22:20:14.23.15:17| |
Structure |
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