Reaction Details |
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Target | Cytochrome P450 2D6 |
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Ligand | BDBM50281371 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1722531 (CHEMBL4137531) |
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IC50 | 600±n/a nM |
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Citation | Embrechts, W; Herschke, F; Pauwels, F; Stoops, B; Last, S; Pieters, S; Pande, V; Pille, G; Amssoms, K; Smyej, I; Dhuyvetter, D; Scholliers, A; Mostmans, W; Van Dijck, K; Van Schoubroeck, B; Thone, T; De Pooter, D; Fanning, G; Jonckers, THM; Horton, H; Raboisson, P; McGowan, D 2,4-Diaminoquinazolines as Dual Toll-like Receptor (TLR) 7/8 Modulators for the Treatment of Hepatitis B Virus. J Med Chem61:6236-6246 (2018) [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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BDBM50281371 |
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n/a |
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Name | BDBM50281371 |
Synonyms: | CHEMBL4171368 |
Type | Small organic molecule |
Emp. Form. | C15H22N4O2 |
Mol. Mass. | 290.3608 |
SMILES | CCC[C@@H](CCO)Nc1nc(N)nc2cc(OC)ccc12 |r| |
Structure |
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