Abstract
The pseudotrisaccharide allosamidin 1 is a potent family-18 chitinase inhibitor, and it demonstrates biological activities against insects and fungi. Recent development for the synthesis and activities of compound 1 and its analogues was reviewed. Huang et al. described the solid-phase synthesis of allosamidin 1 and its analogues, which were obtained by iterative glycosylation reactions, catalytic hydrogenation, acetylation, and deacetylation, respectively. It indicated that di-N-acetyl-β-chitobiosyl allosamizoline was strongly against insect chitinase from Bombyx mori. Withers and his coworkers have synthesized chitobiose and chitotriose thiazolines, which exhibit chitinase inhibition activity.
Keywords: Allosamidin, analogues, synthesis, activities, recent development, β-linked, N-iodosuccinimide, oligosaccharides, trimethylsilyl trifluromethanesulfonate
Mini-Reviews in Medicinal Chemistry
Title:Recent Progress on Synthesis and Activities of Allosamidin and Its Analogues
Volume: 12 Issue: 7
Author(s): Gangliang Huang
Affiliation:
Keywords: Allosamidin, analogues, synthesis, activities, recent development, β-linked, N-iodosuccinimide, oligosaccharides, trimethylsilyl trifluromethanesulfonate
Abstract: The pseudotrisaccharide allosamidin 1 is a potent family-18 chitinase inhibitor, and it demonstrates biological activities against insects and fungi. Recent development for the synthesis and activities of compound 1 and its analogues was reviewed. Huang et al. described the solid-phase synthesis of allosamidin 1 and its analogues, which were obtained by iterative glycosylation reactions, catalytic hydrogenation, acetylation, and deacetylation, respectively. It indicated that di-N-acetyl-β-chitobiosyl allosamizoline was strongly against insect chitinase from Bombyx mori. Withers and his coworkers have synthesized chitobiose and chitotriose thiazolines, which exhibit chitinase inhibition activity.
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Cite this article as:
Huang Gangliang, Recent Progress on Synthesis and Activities of Allosamidin and Its Analogues, Mini-Reviews in Medicinal Chemistry 2012; 12 (7) . https://dx.doi.org/10.2174/138955712800626700
DOI https://dx.doi.org/10.2174/138955712800626700 |
Print ISSN 1389-5575 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5607 |
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