Reaction Details |
| Report a problem with these data |
Target | Cytochrome P450 1A1 |
---|
Ligand | BDBM50585333 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_2162106 (CHEMBL5046967) |
---|
Ki | 1700±n/a nM |
---|
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 |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Cytochrome P450 1A1 |
---|
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
|
|
|
BDBM50585333 |
---|
n/a |
---|
Name | BDBM50585333 |
Synonyms: | CHEMBL5084275 |
Type | Small organic molecule |
Emp. Form. | C22H28N2O7S |
Mol. Mass. | 464.532 |
SMILES | COc1cc(OS(=O)(=O)c2ccc(cc2)N2CCN(CC(C)C)C2=O)cc(OC)c1OC |
Structure |
|