オバタケ キヨウコ
大畠 京子 所属 薬学部 薬学科 職種 教授 |
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言語種別 | 英語 |
発行・発表の年月 | 2014/12 |
形態種別 | 学術論文 |
査読 | 査読あり |
標題 | Iminosugar-Based Galactoside Mimics as Inhibitors of Galactocerebrosidase: SAR Studies and Comparison with Other Lysosomal Galactosidases. |
執筆形態 | 共著 |
掲載誌名 | ChemMedChem. |
巻・号・頁 | 9(12),pp.2647-2652 |
著者・共著者 | Biela-Banaś A., Oulaïdi F., Front S., Gallienne E., Ikeda-Obatake K., Asano N., Wenger D. A. , Martin O. R. |
概要 | Several families of iminosugar-based galactoside mimics were designed, synthesized, and evaluated as galactocerebrosidase (GALC) inhibitors. They were also tested as inhibitors of lysosomal beta- and alpha-galactosidases in order to find new potent and selective pharmacological chaperones for treatment of the lysosomal storage disorder, Krabbe disease. Whereas 1-C-alkyl imino-L-arabinitols are totally inactive toward the three enzymes, 1-C-alkyl imino-D-galactitols were found to be active only toward alpha-galactosidase A. Finally, 1-N-iminosugars provided the best results, as 4-epi-isofagomine was found to be a good inhibitor of both lysosomal beta-galactosidase and GALC. Further elaboration of this structure is required to achieve selectivity between these two galactosidases. |