Giant Glycosidase Inhibitors: First- and Second-Generation Fullerodendrimers with a Dense Iminosugar Shell

被引:35
作者
Nierengarten, Jean-Francois [1 ,2 ]
Schneider, Jeremy P. [2 ,3 ]
Thi Minh Nguyet Trinh [1 ,2 ]
Joosten, Antoine [2 ,3 ]
Holler, Michel [1 ,2 ]
Lepage, Mathieu L. [2 ,3 ]
Bodlenner, Anne [2 ,3 ]
Garcia-Moreno, M. Isabel [4 ]
Ortiz Mellet, Carmen [4 ]
Compain, Philippe [2 ,3 ]
机构
[1] Univ Strasbourg, Lab Chim Mat Mol, 25 Rue Becquerel, F-67087 Strasbourg 2, France
[2] Ecole Europenne Chim Polymeres & Mat, CNRS, UMR 7509, 25 Rue Becquerel, F-67087 Strasbourg 2, France
[3] Univ Strasbourg, Lab Synth Organ & Mol Bioact, 25 Rue Becquerel, F-67087 Strasbourg 2, France
[4] Univ Seville, Fac Quim, Dept Quim Organ, Prof Garcia Gonzalez 1, E-41012 Seville, Spain
关键词
dendrimers; fullerenes; glycosidase inhibition; iminosugars; multivalent effects; CARBOHYDRATE-PROCESSING ENZYMES; BETA-GLUCOCEREBROSIDASE ACTIVITY; CATALYZED ALKYNE-AZIDE; PHARMACOLOGICAL CHAPERONES; CLICK CLUSTERS; CHEMOTHERAPEUTIC VALUE; GAUCHER-DISEASE; MULTIVALENT IMINOSUGARS; PROTEIN INTERACTIONS; EMERGING TRENDS;
D O I
10.1002/chem.201705600
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The multivalent effect in glycosidase inhibition is a new topic in glycoscience that has emerged a few years ago, with the discovery of neoglycoclusters displaying strong binding enhancements over the corresponding monovalent inhibitor. Iminosugar-fullerene conjugates with high valencies have been prepared from iminosugar-terminated dendrons and a clickable fullerene hexa-adduct scaffold. The simultaneous grafting of twelve dendrons allows for a very fast dendritic growth thus limiting the number of synthetic steps required to prepare compounds with a high number of peripheral units. The grafting of first- and second-generation dendrons provided fullerodendrimers surrounded by 36 and 108 peripheral iminosugars, respectively. Inhibition studies have been carried out with a panel of glycosidases. In the particular case of Jack bean alpha-mannosidase, the 108-valent nanoconstruct displays inhibition in the nanomolar range and an additional binding enhancement of one order of magnitude when compared to the 36-valent analogues.
引用
收藏
页码:2483 / 2492
页数:10
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