Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pseudo-oligosaccharides

Potassium native gellan, 389-391,430-431 Pseudo-oligosaccharides, spirodioxanyl, 220-221 Pyramine... [Pg.489]

Aminoglycoside antibiotics represent a family of highly charged naturally occurring pseudo-oligosaccharides (Figure 10.2). The common core of most... [Pg.269]

Recently, pseudo-oligosaccharidic enzyme-inhibitors acarbose (3) [6], trestatins (4) [7], adiposins (5) [8], S-AI [9, 10], and oligostatins [11, 12] have been found in fermentation beers (Scheme 3, 4, 5). [Pg.258]

The methylacarviosin 447, a core structure of acarbose and related pseudo-oligosaccharidic a-amylase inhibitors, together with its 6-hydroxy analog 448, were prepared by Shibata et al. [257] from the corresponding oligobiosaminide derivatives 443 and 444. The aziridine intermediates 445 and 446 were treated with hydrochloric acid to give the corresponding 6 -chloro derivative, and then elimination of the chlorine by base fmnished the title compoimds 447 and 448 as peracetylated derivatives (compoimds 441-448). [Pg.415]

In a broader perspective a plethora of the alcoholic functions of the 1,3-diaminoinositol ie., the pharmacophoric moiety are strategically substituted via various glucosidic bonds studded with appropriate characteristic aminosugars to give rise to the production of pseudo-oligosaccharides. [Pg.789]

A number of amylase inhibitors have been reported these are proteins, glycoproteins or pseudo-oligosaccharides isolated originally from grains or microorganisms. Acarbose, Bay g 5421 is the most... [Pg.161]

J. M. Garcia Fernandez, C. O. Mellet, V. M. Diaz Perez, J. Fuentes, J. Kovacs, and I. Pinter, Synthesis of (1 -6)-carbodiimide-tethered pseudo oligosaccharides via aza-Wittig reaction, Carbohydr. Res, 304 (1997) 261-270. [Pg.177]

In another nice contribution the sialylation of cyclic pseudo-oligosaccharides, derived by click chemistry, by use of TcTS and MU-Neu5Ac were studied to give di- as well as tri-sialylated products. In all cases a-sialylation was obtained at all terminal Gal-3-positions (Fig. 7) [43]. [Pg.238]


See other pages where Pseudo-oligosaccharides is mentioned: [Pg.207]    [Pg.208]    [Pg.220]    [Pg.223]    [Pg.230]    [Pg.485]    [Pg.490]    [Pg.22]    [Pg.348]    [Pg.115]    [Pg.2343]    [Pg.154]    [Pg.158]    [Pg.158]    [Pg.160]    [Pg.318]    [Pg.322]    [Pg.1624]    [Pg.61]    [Pg.84]    [Pg.113]    [Pg.121]    [Pg.127]    [Pg.129]    [Pg.134]    [Pg.351]    [Pg.383]   
See also in sourсe #XX -- [ Pg.348 ]

See also in sourсe #XX -- [ Pg.289 ]

See also in sourсe #XX -- [ Pg.48 , Pg.348 ]

See also in sourсe #XX -- [ Pg.13 , Pg.23 ]

See also in sourсe #XX -- [ Pg.13 , Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.239 , Pg.240 , Pg.241 , Pg.242 , Pg.243 , Pg.244 , Pg.245 ]

See also in sourсe #XX -- [ Pg.789 ]

See also in sourсe #XX -- [ Pg.289 ]




SEARCH



Of pseudo-oligosaccharide

Pseudo-oligosaccharide inhibitor

Pseudo-oligosaccharides synthesis

© 2024 chempedia.info