Reaction Details |
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Target | Cytochrome P450 2D6 |
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Ligand | BDBM50419356 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_788271 (CHEMBL1919534) |
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IC50 | <10000±n/a nM |
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Citation | Morley, AD; Cook, A; King, S; Roberts, B; Lever, S; Weaver, R; Macdonald, C; Unitt, J; Fagura, M; Phillips, T; Lewis, R; Wenlock, M Discovery of pyrazoles as novel FPR1 antagonists. Bioorg Med Chem Lett21:6456-60 (2011) [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 |
Synonyms: | CP2D6_HUMAN | CYP2D6 | CYP2DL1 | CYPIID6 | Cytochrome P450 2D6 (CYP2D6) | Debrisoquine 4-hydroxylase | P450-DB1 |
Type: | Protein |
Mol. Mass.: | 55774.82 |
Organism: | Homo sapiens (Human) |
Description: | P10635 |
Residue: | 497 |
Sequence: | MGLEALVPLAVIVAIFLLLVDLMHRRQRWAARYPPGPLPLPGLGNLLHVDFQNTPYCFDQ
LRRRFGDVFSLQLAWTPVVVLNGLAAVREALVTHGEDTADRPPVPITQILGFGPRSQGVF
LARYGPAWREQRRFSVSTLRNLGLGKKSLEQWVTEEAACLCAAFANHSGRPFRPNGLLDK
AVSNVIASLTCGRRFEYDDPRFLRLLDLAQEGLKEESGFLREVLNAVPVLLHIPALAGKV
LRFQKAFLTQLDELLTEHRMTWDPAQPPRDLTEAFLAEMEKAKGNPESSFNDENLRIVVA
DLFSAGMVTTSTTLAWGLLLMILHPDVQRRVQQEIDDVIGQVRRPEMGDQAHMPYTTAVI
HEVQRFGDIVPLGVTHMTSRDIEVQGFRIPKGTTLITNLSSVLKDEAVWEKPFRFHPEHF
LDAQGHFVKPEAFLPFSAGRRACLGEPLARMELFLFFTSLLQHFSFSVPTGQPRPSHHGV
FAFLVSPSPYELCAVPR
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BDBM50419356 |
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n/a |
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Name | BDBM50419356 |
Synonyms: | CHEMBL1916288 |
Type | Small organic molecule |
Emp. Form. | C24H26FN5O3S |
Mol. Mass. | 483.558 |
SMILES | C[C@H](NC(=O)c1c(C)nn(c1NS(=O)(=O)c1ccc(cc1)C#N)-c1ccc(F)cc1)C(C)(C)C |r| |
Structure |
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