Reaction Details |
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Target | Cytochrome P450 2J2 |
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Ligand | BDBM50319987 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_635054 (CHEMBL1119168) |
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IC50 | 10000±n/a nM |
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Citation | Kowalski, JA; Swinamer, AD; Muegge, I; Eldrup, AB; Kukulka, A; Cywin, CL; De Lombaert, S Rapid synthesis of an array of trisubstituted urea-based soluble epoxide hydrolase inhibitors facilitated by a novel solid-phase method. Bioorg Med Chem Lett20:3703-7 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 2J2 |
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Name: | Cytochrome P450 2J2 |
Synonyms: | CP2J2_HUMAN | CYP2J2 |
Type: | Enzyme |
Mol. Mass.: | 57623.04 |
Organism: | Homo sapiens (Human) |
Description: | P51589 |
Residue: | 502 |
Sequence: | MLAAMGSLAAALWAVVHPRTLLLGTVAFLLAADFLKRRRPKNYPPGPWRLPFLGNFFLVD
FEQSHLEVQLFVKKYGNLFSLELGDISAVLITGLPLIKEALIHMDQNFGNRPVTPMREHI
FKKNGLIMSSGQAWKEQRRFTLTALRNFGLGKKSLEERIQEEAQHLTEAIKEENGQPFDP
HFKINNAVSNIICSITFGERFEYQDSWFQQLLKLLDEVTYLEASKTCQLYNVFPWIMKFL
PGPHQTLFSNWKKLKLFVSHMIDKHRKDWNPAETRDFIDAYLKEMSKHTGNPTSSFHEEN
LICSTLDLFFAGTETTSTTLRWALLYMALYPEIQEKVQAEIDRVIGQGQQPSTAARESMP
YTNAVIHEVQRMGNIIPLNVPREVTVDTTLAGYHLPKGTMILTNLTALHRDPTEWATPDT
FNPDHFLENGQFKKREAFMPFSIGKRACLGEQLARTELFIFFTSLMQKFTFRPPNNEKLS
LKFRMGITISPVSHRLCAVPQV
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BDBM50319987 |
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n/a |
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Name | BDBM50319987 |
Synonyms: | 4-(pyridin-4-yloxy)-N-(2-(trifluoromethoxy)benzyl)piperidine-1-carboxamide | CHEMBL1085744 |
Type | Small organic molecule |
Emp. Form. | C19H20F3N3O3 |
Mol. Mass. | 395.3756 |
SMILES | FC(F)(F)Oc1ccccc1CNC(=O)N1CCC(CC1)Oc1ccncc1 |
Structure |
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