| Reaction Details |
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 | Report a problem with these data |
| Target | Cytochrome P450 2D6 |
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| Ligand | BDBM50443778 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1280376 (CHEMBL3095536) |
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| IC50 | 13000±n/a nM |
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| Citation |  Wilson, DM; Apps, J; Bailey, N; Bamford, MJ; Beresford, IJ; Briggs, MA; Calver, AR; Crook, B; Davis, RP; Davis, S; Dean, DK; Harris, L; Heightman, TD; Panchal, T; Parr, CA; Quashie, N; Steadman, JG; Schogger, J; Sehmi, SS; Stean, TO; Takle, AK; Trail, BK; White, T; Witherington, J; Worby, A; Medhurst, AD The discovery of the benzazepine class of histamine H3 receptor antagonists. Bioorg Med Chem Lett23:6897-901 (2013) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Cytochrome P450 2D6 |
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| Name: | Cytochrome P450 2D6 |
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| Synonyms: | CP2D6_HUMAN | CYP2D6 | CYP2DL1 | CYPIID6 | Cytochrome P450 2D6 (CYP2D6) | Debrisoquine 4-hydroxylase | P450-DB1 |
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| Type: | Protein |
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| Mol. Mass.: | 55774.82 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P10635 |
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| Residue: | 497 |
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| Sequence: | MGLEALVPLAVIVAIFLLLVDLMHRRQRWAARYPPGPLPLPGLGNLLHVDFQNTPYCFDQ
LRRRFGDVFSLQLAWTPVVVLNGLAAVREALVTHGEDTADRPPVPITQILGFGPRSQGVF
LARYGPAWREQRRFSVSTLRNLGLGKKSLEQWVTEEAACLCAAFANHSGRPFRPNGLLDK
AVSNVIASLTCGRRFEYDDPRFLRLLDLAQEGLKEESGFLREVLNAVPVLLHIPALAGKV
LRFQKAFLTQLDELLTEHRMTWDPAQPPRDLTEAFLAEMEKAKGNPESSFNDENLRIVVA
DLFSAGMVTTSTTLAWGLLLMILHPDVQRRVQQEIDDVIGQVRRPEMGDQAHMPYTTAVI
HEVQRFGDIVPLGVTHMTSRDIEVQGFRIPKGTTLITNLSSVLKDEAVWEKPFRFHPEHF
LDAQGHFVKPEAFLPFSAGRRACLGEPLARMELFLFFTSLLQHFSFSVPTGQPRPSHHGV
FAFLVSPSPYELCAVPR
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| BDBM50443778 |
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| n/a |
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| Name | BDBM50443778 |
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| Synonyms: | CHEMBL3094125 |
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| Type | Small organic molecule |
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| Emp. Form. | C20H30N2O3S |
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| Mol. Mass. | 378.529 |
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| SMILES | CS(=O)(=O)N1CCC(CC1)Oc1ccc2CCN(CCc2c1)C1CCC1 |
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| Structure | 
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