Reaction Details |
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Target | Cytochrome P450 2D6 |
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Ligand | BDBM50548670 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2022782 (CHEMBL4676595) |
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IC50 | >10000±n/a nM |
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Citation | Soth, MJ; Le, K; Di Francesco, ME; Hamilton, MM; Liu, G; Burke, JP; Carroll, CL; Kovacs, JJ; Bardenhagen, JP; Bristow, CA; Cardozo, M; Czako, B; de Stanchina, E; Feng, N; Garvey, JR; Gay, JP; Do, MKG; Greer, J; Han, M; Harris, A; Herrera, Z; Huang, S; Giuliani, V; Jiang, Y; Johnson, SB; Johnson, TA; Kang, Z; Leonard, PG; Liu, Z; McAfoos, T; Miller, M; Morlacchi, P; Mullinax, RA; Palmer, WS; Pang, J; Rogers, N; Rudin, CM; Shepard, HE; Spencer, ND; Theroff, J; Wu, Q; Xu, A; Yau, JA; Draetta, G; Toniatti, C; Heffernan, TP; Jones, P Discovery of IPN60090, a Clinical Stage Selective Glutaminase-1 (GLS-1) Inhibitor with Excellent Pharmacokinetic and Physicochemical Properties. J Med Chem63:12957-12977 (2020) [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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BDBM50548670 |
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n/a |
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Name | BDBM50548670 |
Synonyms: | CHEMBL4741924 |
Type | Small organic molecule |
Emp. Form. | C24H27F3N8O3 |
Mol. Mass. | 532.5182 |
SMILES | CNC(=O)c1cn(C[C@H](F)CCc2ccc(NC(=O)Cc3cc(OC4CC(F)(F)C4)cc(C)n3)nn2)nn1 |r| |
Structure |
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