Reaction Details |
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Target | Bifunctional epoxide hydrolase 2 |
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Ligand | BDBM50133697 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1526369 (CHEMBL3637430) |
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IC50 | 45±n/a nM |
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Citation | Burmistrov, V; Morisseau, C; Danilov, D; Harris, TR; Dalinger, I; Vatsadze, I; Shkineva, T; Butov, GM; Hammock, BD 1,3-Disubstituted and 1,3,3-trisubstituted adamantyl-ureas with isoxazole as soluble epoxide hydrolase inhibitors. Bioorg Med Chem Lett25:5514-9 (2015) [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: | Cytosolic epoxide hydrolase 2 | EBifunctional epoxide hydrolase 2 | EPHX2 | Epoxide hydratase | HYES_HUMAN | Lipid-phosphate phosphatase | Soluble epoxide hydrolase (sEH) | epoxide hydrolase 2, cytoplasmic |
Type: | Enzyme |
Mol. Mass.: | 62613.07 |
Organism: | Homo sapiens (Human) |
Description: | P34913 |
Residue: | 555 |
Sequence: | MTLRAAVFDLDGVLALPAVFGVLGRTEEALALPRGLLNDAFQKGGPEGATTRLMKGEITL
SQWIPLMEENCRKCSETAKVCLPKNFSIKEIFDKAISARKINRPMLQAALMLRKKGFTTA
ILTNTWLDDRAERDGLAQLMCELKMHFDFLIESCQVGMVKPEPQIYKFLLDTLKASPSEV
VFLDDIGANLKPARDLGMVTILVQDTDTALKELEKVTGIQLLNTPAPLPTSCNPSDMSHG
YVTVKPRVRLHFVELGSGPAVCLCHGFPESWYSWRYQIPALAQAGYRVLAMDMKGYGESS
APPEIEEYCMEVLCKEMVTFLDKLGLSQAVFIGHDWGGMLVWYMALFYPERVRAVASLNT
PFIPANPNMSPLESIKANPVFDYQLYFQEPGVAEAELEQNLSRTFKSLFRASDESVLSMH
KVCEAGGLFVNSPEEPSLSRMVTEEEIQFYVQQFKKSGFRGPLNWYRNMERNWKWACKSL
GRKILIPALMVTAEKDFVLVPQMSQHMEDWIPHLKRGHIEDCGHWTQMDKPTEVNQILIK
WLDSDARNPPVVSKM
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BDBM50133697 |
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n/a |
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Name | BDBM50133697 |
Synonyms: | CHEMBL3633671 |
Type | Small organic molecule |
Emp. Form. | C19H29N3O2 |
Mol. Mass. | 331.4525 |
SMILES | CC(C)c1cc(CNC(=O)NCC23CC4CC(CC(C4)C2)C3)on1 |TLB:19:14:21:18.17.20,19:18:21:15.14.13,THB:17:16:13:19.18.20,17:18:15.16.21:13| |
Structure |
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