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D-Glucuronate

Gum ghatti is the calcium and magnesium salt of a complex polysaccharide which contains L-arabinose, D-galactose, D-mannose, and D-xylose and D-glucuronic acid (48) and has a molecular weight of approximately 12,000. On dispersion in water, gum ghatti forms viscous solutions of viscosity intermediate between those of gum arabic and gum karaya. These dispersions have emulsification and adhesive properties equivalent to or superior to those described for gum arabic. [Pg.434]

Uronic acids are monosaccharides in which the terminal primary alcohol group is oxidized to a carboxyhc acid functional group, eg, D-glucuronic acid [6556-12-3] (11). [Pg.481]

P -D-xylan with 3-hnked a-L-arabiaose branches (1 4)-P -D-xylan with 2-Unked 4-0-methyl-a-D-glucuronic acid and arabiaose branches... [Pg.70]

Monosaccharides can be oxidized enzymatically at C-6, yielding uronic acids, such as D-glucuronic and L-iduronic acids (Figure 7.10). L-Iduronic acid is similar to D-glucuronic acid, except for having an opposite configuration at C-5. Oxidation at both C-1 and C-6 produces aldaric acids, such as D-glucaric... [Pg.217]

An exopolysaccharide containing a high content of D-glucuronic add will tend to bind cations. [Pg.198]

Figure 2 Structures of D-glucuronic (GlucA 1), o-galacturonic (GalA 2), and o-gluconic (GluA 3) acids. Figure 2 Structures of D-glucuronic (GlucA 1), o-galacturonic (GalA 2), and o-gluconic (GluA 3) acids.
CN D-glucuronic acid compd. with 5-methyl-6-[[(3,4,5-trimethoxyphenyl)amino]methyl]-2,4-quinazolinediamine (1 1)... [Pg.2120]

C4()H7,jOi9 17575-20-1) see Acetyldigitoxin a-Acetyldigoxin Lanatoside C D-glucuronic acid... [Pg.2390]

The NMR spectrum of the dry sample showed broad unresolved peaks that correspond to a typical mixture of 4-O-methyl-D-glucuronic acid, L-arabinose and D-xylose, and proteins (Oliveira et al., 2010) (Figure 5). [Pg.68]


See other pages where D-Glucuronate is mentioned: [Pg.97]    [Pg.207]    [Pg.414]    [Pg.1055]    [Pg.1055]    [Pg.434]    [Pg.436]    [Pg.31]    [Pg.32]    [Pg.296]    [Pg.298]    [Pg.18]    [Pg.19]    [Pg.19]    [Pg.19]    [Pg.20]    [Pg.176]    [Pg.475]    [Pg.481]    [Pg.484]    [Pg.251]    [Pg.1055]    [Pg.1055]    [Pg.218]    [Pg.234]    [Pg.252]    [Pg.994]    [Pg.197]    [Pg.199]    [Pg.7]    [Pg.10]    [Pg.14]    [Pg.108]    [Pg.382]    [Pg.3]    [Pg.3]    [Pg.6]    [Pg.370]    [Pg.432]    [Pg.293]   
See also in sourсe #XX -- [ Pg.105 , Pg.106 ]

See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.55 ]

See also in sourсe #XX -- [ Pg.236 ]

See also in sourсe #XX -- [ Pg.320 ]




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4-0-Methyl-D-glucuronic acid

4-O-Methyl-D-glucuronic acid

4-O-Methyl-D-glucuronic acid residues

Animals conjugates of D-glucuronic acid originating

Conjugates of D-glucuronic acid

D Glucuronic acid

D-Glucurone

D-Glucurone

D-Glucuronic acid 2-amino-2-deoxy

D-Glucuronic acid accumulation

D-Glucuronic acid catabolism

D-Glucuronic acid in metabolism

D-Glucuronic acid lactone

D-Glucuronic acid metabolism of, scheme

D-Glucuronic acid methyl ester

D-glucuronic acid residues

Glucuronate

Glucuronates

Glucurone

Glucuronic

Mehltretter, C. L., The Chemical Synthesis of D-Glucuronic Acid

Metabolism D-glucuronic acid

Of D-glucuronic acid

P-D-Glucuronic acid

Synthesis chemical, of D-glucuronic acid

The Chemical Synthesis of D-Glucuronic Acid

UDP-D-glucuronic acid

Uridine diphosphate D-glucuronic acid

Uridine-5 ’ -diphospho-a -d-glucuronic acid

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