Reaction Details |
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Target | Cytochrome P450 1A1 |
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Ligand | BDBM50585332 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2162106 (CHEMBL5046967) |
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Ki | 300±n/a nM |
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Citation | Bouzriba, C; Chavez Alvarez, AC; Gagné-Boulet, M; Ouellette, V; Lacroix, J; Côté, MF; C-Gaudreault, R; Fortin, S Branched alkyl of phenyl 4-(2-oxo-3-alkylimidazolidin-1-yl)benzenesulfonates as unique cytochrome P450 1A1-activated antimitotic prodrugs: Biological evaluation and mechanism of bioactivation. Eur J Med Chem229:0 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 1A1 |
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Name: | Cytochrome P450 1A1 |
Synonyms: | CP1A1_HUMAN | CYP1A1 | CYPIA1 | Cytochrome P450 1A | Cytochrome P450 1A1 | Cytochrome P450 1A1 (CYP1A1) | P450 form 6 | P450-C | P450-P1 |
Type: | Protein |
Mol. Mass.: | 58177.23 |
Organism: | Homo sapiens (Human) |
Description: | P04798 |
Residue: | 512 |
Sequence: | MLFPISMSATEFLLASVIFCLVFWVIRASRPQVPKGLKNPPGPWGWPLIGHMLTLGKNPH
LALSRMSQQYGDVLQIRIGSTPVVVLSGLDTIRQALVRQGDDFKGRPDLYTFTLISNGQS
MSFSPDSGPVWAARRRLAQNGLKSFSIASDPASSTSCYLEEHVSKEAEVLISTLQELMAG
PGHFNPYRYVVVSVTNVICAICFGRRYDHNHQELLSLVNLNNNFGEVVGSGNPADFIPIL
RYLPNPSLNAFKDLNEKFYSFMQKMVKEHYKTFEKGHIRDITDSLIEHCQEKQLDENANV
QLSDEKIINIVLDLFGAGFDTVTTAISWSLMYLVMNPRVQRKIQEELDTVIGRSRRPRLS
DRSHLPYMEAFILETFRHSSFVPFTIPHSTTRDTSLKGFYIPKGRCVFVNQWQINHDQKL
WVNPSEFLPERFLTPDGAIDKVLSEKVIIFGMGKRKCIGETIARWEVFLFLAILLQRVEF
SVPLGVKVDMTPIYGLTMKHACCEHFQMQLRS
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BDBM50585332 |
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n/a |
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Name | BDBM50585332 |
Synonyms: | CHEMBL5077719 |
Type | Small organic molecule |
Emp. Form. | C19H20Br2N2O4S |
Mol. Mass. | 532.246 |
SMILES | CC(C)CN1CCN(C1=O)c1ccc(cc1)S(=O)(=O)Oc1cc(Br)cc(Br)c1 |
Structure |
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