Reaction Details |
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Target | Cytochrome P450 2D6 |
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Ligand | BDBM124951 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1930557 (CHEMBL4433808) |
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IC50 | >31000±n/a nM |
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Citation | Papeo, G; Orsini, P; Avanzi, NR; Borghi, D; Casale, E; Ciomei, M; Cirla, A; Desperati, V; Donati, D; Felder, ER; Galvani, A; Guanci, M; Isacchi, A; Posteri, H; Rainoldi, S; Riccardi-Sirtori, F; Scolaro, A; Montagnoli, A Discovery of Stereospecific PARP-1 Inhibitor Isoindolinone NMS-P515. ACS Med Chem Lett10:534-538 (2019) [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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BDBM124951 |
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n/a |
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Name | BDBM124951 |
Synonyms: | US8765972, 4 |
Type | Small organic molecule |
Emp. Form. | C21H29N3O2 |
Mol. Mass. | 355.4739 |
SMILES | C[C@@H]1N(C2CCN(CC2)C2CCCCC2)C(=O)c2c1cccc2C(N)=O |r| |
Structure |
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