Iminosugar-Based Galactoside Mimics as Inhibitors of Galactocerebrosidase: SAR Studies and Comparison with Other Lysosomal Galactosidases

被引:20
作者
Biela-Banas, Anna [1 ,2 ]
Oulaidi, Farah [1 ,2 ]
Front, Sophie [1 ,2 ]
Gallienne, Estelle [1 ,2 ]
Ikeda-Obatake, Kyoko [3 ]
Asano, Naoki [3 ]
Wenger, David A. [4 ]
Martin, Olivier R. [1 ,2 ]
机构
[1] Univ Orleans, UMR 7311, ICOA, F-45067 Orleans 2, France
[2] Univ Orleans, CNRS, F-45067 Orleans 2, France
[3] Hokuriku Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 9201181, Japan
[4] Thomas Jefferson Univ, Jefferson Med Coll, Dept Neurol, Philadelphia, PA 19107 USA
关键词
galactocerebrosidase; iminosugars; inhibitors; Krabbe disease; pharmacological chaperones; GLOBOID-CELL LEUKODYSTROPHY; KRABBE-DISEASE; PHARMACOLOGICAL CHAPERONES; FABRY DISEASE; STEREOSELECTIVE-SYNTHESIS; BETA-GALACTOSIDASE; L-ARABINITOL; MOUSE MODEL; D-XYLITOL; ISOFAGOMINE;
D O I
10.1002/cmdc.201402411
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several families of iminosugar-based galactoside mimics were designed, synthesized, and evaluated as galactocerebrosidase (GALC) inhibitors. They were also tested as inhibitors of lysosomal - and -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 -galactosidaseA. Finally, 1-N-iminosugars provided the best results, as 4-epi-isofagomine was found to be a good inhibitor of both lysosomal -galactosidase and GALC. Further elaboration of this structure is required to achieve selectivity between these two galactosidases.
引用
收藏
页码:2647 / 2652
页数:6
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