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- W1539260711 abstract "Publisher Summary This chapter discusses the calystegines. The structural and chemical properties of calystegines are discussed. After the examination of numerous species in the families Solanaceae and Convolvulaceae, and of Morus species in the Moraceae, 14 different alkaloids named as calystegines are distinguished, in addition to two, naturally occurring calystegine glycosides. Assignment of individual structures into the sections of calystegines A, B, and C depends on the number of three to five hydroxyl groups, respectively. Calystegines were initially detected in the course of a search for opines and other nutritional mediators in plant roots. Subsequent calystegine isolations followed enrichment schemes that were developed for the isolation of other polyhydroxy alkaloids, such as swainsonine and 1-deoxynojirimycin from S. canescens (Fabaceae) and from Streptomyces strains, respectively. The occurrence of calystegines in the plant kingdom is briefly discussed. Calystegines, like other monosaccharide-mimicking alkaloids, inhibit glycosidases due to their similarity to the pyranose moieties of the natural substrates. Biochemical activities and therapeutic applications for this class of natural compounds are reviewed. Enzymatic processing of carbohydrates in plants is catalyzed by a variety of carbohydrate-active enzymes, including glycosidases, glycosyl transferases, polysaccharide lyases, and carbohydrate esterases. Such enzymes may also be produced by microbial plant pathogens and insects and increase their virulence or herbivory, respectively." @default.
- W1539260711 created "2016-06-24" @default.
- W1539260711 creator A5025847122 @default.
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- W1539260711 date "2007-01-01" @default.
- W1539260711 modified "2023-10-18" @default.
- W1539260711 title "Chapter 2 Calystegines" @default.
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