Synthesis of 1,5-dideoxy-3-O-(α-D-mannopyranosyl)-1,5-imino-D-mannitol and 1,5-dideoxy-3-O-(α-D-glucopyranosyl)-1,5-imino-D-mannitol: Powerful inhibitors of endomannosidase
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (9) , 2011-2024
- https://doi.org/10.1016/s0957-4166(00)82250-8
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- The structural basis of the inhibition of human α-mannosidases by azafuranose analogues of mannoseBiochemical Journal, 1993
- Anomeric specificity of D-xylose isomeraseBiochemistry, 1992
- Amino-sugar glycosidase inhibitors: versatile tools for glycobiologistsGlycobiology, 1992
- Iminoheptitols as glycosidase inhibitors: Synthesis of α-homomannojirimycin, 6-epi-α-homomannojirimycin and of a highly substituted pipecolic acidTetrahedron, 1992
- Inhibition of α-mannosidases by seven carbon sugars: Synthesis of some seven carbon analogues of mannofuranoseTetrahedron, 1992
- ANTI-HIV ACTIVITY OF CASTANOSPERMINE ANALOGUESThe Lancet, 1989
- Aminosugar derivatives as potential anti-human immunodeficiency virus agents.Proceedings of the National Academy of Sciences, 1988
- Inhibition of human immunodeficiency virus syncytium formation and virus replication by castanospermine.Proceedings of the National Academy of Sciences, 1987
- CASTANOSPERMINE AND OTHER PLANT ALKALOID INHIBITORS OF GLUCOSIDASE ACTIVITY BLOCK THE GROWTH OF HIVThe Lancet, 1987
- ASSEMBLY OF ASPARAGINE-LINKED OLIGOSACCHARIDESAnnual Review of Biochemistry, 1985