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Glucurone

Glycoproteins or mucoproieins. Compounds of proteins with carbohydrates. All glycoproteins contain a hexosamine and usually sulphate, ethanoate and glucuronic acid. The carbohydrate-protein linkages are, in some cases covalent and in others of the salt type. Aqueous solutions of glycoproteins are extremely viscous. [Pg.332]

They are found in a great variety of plants and are strong fish poisons. On hydrolysis they yield a variety of sugars, frequently several molecules to each aglucone. Glucose, galactose, arabinose are the more common pentoses, methylpentoses and glucuronic acid are also obtained. [Pg.352]

Uronic acids are biosynthetic intermediates m various metabolic processes ascorbic acid (vitamin C) for example is biosynthesized by way of glucuronic acid Many metabolic waste products are excreted m the urine as their glucuronate salts... [Pg.1055]

A.- ng deduction. This is an irreversible reaction which is a foremost determinant of the secretion rate of cortisol (double bonds and C-3 carbonyl). Catalyzed predominantiy by cortisone P-reductase and 3a-hydroxysteroid dehydrogenases, SP sterols result, although 5a sterols are more prevalent in the case of other glucocorticoids. Urocortisol and urocortisone result from the metabohsm of cortisol and cortisone, respectively. Compounds can be complexed to glucuronic acid at this point. [Pg.97]

Glucuronidation. Complexation of the steroid to glucuronic acid, most predominantiy via the C-3 hydroxyl, leads to a considerable portion of the excreted metabohtes of ah. glucocorticoids. In infants, sulfurylation (formation of a sulfate ester) is also predominant (16). [Pg.97]

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]

Glc = glucose GlcA = glucuronic acid GulA = guluronic acid Man = mannose ManA = mannuronic acid Rha = rhamnose Xyl = xylose Fuc = fucose. Chemical structures and properties are available (19). [Pg.73]


See other pages where Glucurone is mentioned: [Pg.97]    [Pg.191]    [Pg.191]    [Pg.197]    [Pg.202]    [Pg.207]    [Pg.207]    [Pg.414]    [Pg.1055]    [Pg.1055]    [Pg.14]    [Pg.434]    [Pg.434]    [Pg.436]    [Pg.436]    [Pg.30]    [Pg.31]    [Pg.31]    [Pg.32]    [Pg.32]    [Pg.32]    [Pg.33]    [Pg.224]    [Pg.242]    [Pg.296]    [Pg.298]    [Pg.18]    [Pg.18]    [Pg.19]    [Pg.19]    [Pg.19]    [Pg.20]    [Pg.20]    [Pg.176]    [Pg.475]    [Pg.481]    [Pg.484]    [Pg.113]    [Pg.71]    [Pg.356]    [Pg.101]   
See also in sourсe #XX -- [ Pg.226 ]




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1-Naphthyl glucuronic acid

4-0-Methyl-D-glucuronic acid

4-O-Methyl-D-glucuronic acid

4-O-Methyl-D-glucuronic acid residues

Activated glucuronate

Amino deoxy glucuronic acids

Amino functions, functional groups glucuronic acid conjugates

Ammonium glucuronate

Animals conjugates of D-glucuronic acid originating

Anti-carbohydrate antibodies glucuronic acid

Azido glucuronic acid

Bioactivation glucuronic acid conjugation

Calcium glucuronate

Carbamates glucuronic acid conjugation

Carboxylic acids functional groups, glucuronic acid

Conjugates of D-glucuronic acid

Conjugation glucuronic acid, mammals

Conjugation of glucuronic acid

D Glucuronic acid

D-Glucuronate

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

Fermentation glucuronic acid

Glucuronate

Glucuronate

Glucuronate degradation

Glucuronate degradation and

Glucuronate isolation

Glucuronate labeled, preparation

Glucuronate metabolism

Glucuronate reductase

Glucuronate transferase

Glucuronate transport

Glucuronate/glucuronic acid

Glucuronate/glucuronic acid bilirubin conjugation with

Glucuronates

Glucuronates

Glucurone labeled, preparation

Glucurone trimethyl

Glucuronic

Glucuronic

Glucuronic 2-amino-2-deoxy

Glucuronic 4-0-methyl

Glucuronic Acid and Sulfate Conjugates of Target Analytes

Glucuronic Glucuronidase

Glucuronic Glucuronidase, preparation

Glucuronic acid

Glucuronic acid 3 anomer

Glucuronic acid 3-Glucuronidase

Glucuronic acid 4-O-methyl

Glucuronic acid assembly

Glucuronic acid bilirubin conjugates

Glucuronic acid biosynthesis

Glucuronic acid blood levels

Glucuronic acid chemical synthesis

Glucuronic acid chemistry

Glucuronic acid color tests

Glucuronic acid conformations

Glucuronic acid conjugates

Glucuronic acid conjugates analysis

Glucuronic acid conjugates desorption

Glucuronic acid conjugates species differences

Glucuronic acid conjugates synthesis

Glucuronic acid conjugates techniques

Glucuronic acid conjugation

Glucuronic acid cycle

Glucuronic acid degradation

Glucuronic acid derivatives

Glucuronic acid determination

Glucuronic acid enzymic phosphorylation

Glucuronic acid epimerization

Glucuronic acid ester

Glucuronic acid gas-liquid chromatography

Glucuronic acid glucuronate epimerization

Glucuronic acid in metabolism

Glucuronic acid in urine

Glucuronic acid isolation, from urine

Glucuronic acid kinetics

Glucuronic acid labeled

Glucuronic acid labeled with

Glucuronic acid lactone

Glucuronic acid metabolism

Glucuronic acid methyl ester

Glucuronic acid methyl ethers, synthesis

Glucuronic acid normal urine

Glucuronic acid occurrence

Glucuronic acid pathway

Glucuronic acid phenols from

Glucuronic acid phosphate

Glucuronic acid preparation

Glucuronic acid preparation and properties

Glucuronic acid residue

Glucuronic acid salts

Glucuronic acid sodium salt

Glucuronic acid synthesis

Glucuronic acid toxicity

Glucuronic acid transfer

Glucuronic acid, 2-acetamido-2-deoxy

Glucuronic acid, 2-acetamido-2-deoxy polymer

Glucuronic acid, 4-deoxysynthesis Diels-Alder reaction

Glucuronic acid, bromination

Glucuronic acid, conjugation with

Glucuronic acid, conjugation with retinoic

Glucuronic acid, detoxification

Glucuronic acid, from glucose

Glucuronic acid, from inositol

Glucuronic acid, glucuronidation

Glucuronic acid, methyl derivatives

Glucuronic acid, steroid conjugation

Glucuronic acid, trichloroacetimidates

Glucuronic acid-1 - -phosphate, substrate

Glucuronic acid-2-sulfatase

Glucuronic acid-l-phosphate

Glucuronic prodrugs

Hydroxyl, functional groups, glucuronic

Hydroxyl, functional groups, glucuronic acid conjugates

L-Glucuronic acid

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

Metabolism D-glucuronic acid

Morphine glucuronic acid conjugate

N-Glucurone

Of D-glucuronic acid

Of glucuronic prodrugs

Oxidative reactions, synthesis glucuronic acid

P-D-Glucuronic acid

P-Glucuronic acid

Phenols conjugation with glucuronic acid

Sugar acids glucuronic acid

Synthesis chemical, of D-glucuronic acid

The Chemical Synthesis of D-Glucuronic Acid

UDP glucuronic acid

UDP-D-glucuronic acid

UDP-Glucuronic acid decarboxylase

UDP-glucuronate

Uridine diphosphate D-glucuronic acid

Uridine diphosphate glucuronate

Uridine diphosphate glucuronate acid

Uridine diphosphate glucuronic acid

Uridine diphosphate glucuronic acid (UDPGA

Uridine diphosphate glucuronic acid conjugation

Uridine diphospho glucuronic acid

Uridine diphospho glucuronic acid UDPGA)

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

Xanthan glucuronic acid

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