Reaction Details |
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Target | Cytochrome P450 4F2 |
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Ligand | BDBM558218 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibition Test for Each Compound of the Present Invention Against 20-HETE Producing Enzymes (CYP4F2 and CYP4A11) |
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IC50 | 6.20±n/a nM |
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Citation | Tanaka, H; Kawamura, M; Hamada, M; Kobashi, Y; Ito, Y; Suzuki, K; Bohno, A; Funayama, K Pyridine compound substituted with azole US Patent US11365192 Publication Date 6/21/2022 |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 4F2 |
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Name: | Cytochrome P450 4F2 |
Synonyms: | 20-HETE synthase | 20-hydroxyeicosatetraenoic acid synthase | Arachidonic acid omega-hydroxylase | CP4F2_HUMAN | CYP4F2 | CYPIVF2 | Cytochrome P450 4F2 | Cytochrome P450-LTB-omega | Leukotriene-B(4) 20-monooxygenase 1 | Leukotriene-B(4) omega-hydroxylase 1 | Phylloquinone omega-hydroxylase CYP4F2 |
Type: | PROTEIN |
Mol. Mass.: | 59859.32 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_10743 |
Residue: | 520 |
Sequence: | MSQLSLSWLGLWPVAASPWLLLLLVGASWLLAHVLAWTYAFYDNCRRLRCFPQPPRRNWF
WGHQGMVNPTEEGMRVLTQLVATYPQGFKVWMGPISPLLSLCHPDIIRSVINASAAIAPK
DKFFYSFLEPWLGDGLLLSAGDKWSRHRRMLTPAFHFNILKPYMKIFNESVNIMHAKWQL
LASEGSACLDMFEHISLMTLDSLQKCVFSFDSHCQEKPSEYIAAILELSALVSKRHHEIL
LHIDFLYYLTPDGQRFRRACRLVHDFTDAVIQERRRTLPSQGVDDFLQAKAKSKTLDFID
VLLLSKDEDGKKLSDEDIRAEADTFMFEGHDTTASGLSWVLYHLAKHPEYQERCRQEVQE
LLKDREPKEIEWDDLAHLPFLTMCMKESLRLHPPVPVISRHVTQDIVLPDGRVIPKGIIC
LISVFGTHHNPAVWPDPEVYDPFRFDPENIKERSPLAFIPFSAGPRNCIGQTFAMAEMKV
VLALTLLRFRVLPDHTEPRRKPELVLRAEGGLWLRVEPLS
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BDBM558218 |
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n/a |
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Name | BDBM558218 |
Synonyms: | 2-Methyl-5-[[6-(1H-pyrazol-5-yl)-3-pyridinyl]oxymethyl]phenol | US11365192, Example 12-1 |
Type | Small organic molecule |
Emp. Form. | C16H15N3O2 |
Mol. Mass. | 281.3092 |
SMILES | Cc1ccc(COc2ccc(nc2)-c2ccn[nH]2)cc1O |
Structure |
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