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Glucuronic acid (from Greek γλεῦκος " sweet wine, must " and οὖρον " urine ") is a uronic acid that was first isolated from urine (hence the name "uronic acid"). It is found in many gums such as gum arabic ( approx. 18%), xanthan, and kombucha tea and is important for the metabolism of microorganisms, plants and animals. Properties.
- C₆H₁₀O₇
- 194.139 g·mol−1
- 159 to 161 °C (318 to 322 °F; 432 to 434 K)
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Glucuronsäure (bzw. Glucuronat ), in biochemischer Darstellung häufig mit GlcA abgekürzt, ist die Uronsäure der D - Glucose, von der sie sich durch die Oxidationsstufe am sechsten Kohlenstoff (C6) unterscheidet, wo eine Carboxygruppe statt einer Hydroxygruppe vorliegt.
- (2S,3S,4S,5R,6R)-3,4,5,6-Tetrahydroxytetrahydropyran-2-carbonsäure
- Glucuronsäure
- farbloser Feststoff
- C₆H₁₀O₇
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Glucuronolactone or Glucurolactone ( INN) is a naturally occurring substance that is an important structural component of nearly all connective tissues. [1] . It is sometimes used in energy drinks.
- C₆H₈O₆
- 176.124 g·mol−1
- 176 to 178 °C (349 to 352 °F; 449 to 451 K)
- 26.9 g/100 mL
Glucuronic acid pathway. The first part consists of synthesis of UDP-glucuronic acid and release of free D-glucuronic acid. The second part is the metabolism of D-glucuronic acid. D-Glucuronic acid is written as both the cyclic hemiacetal and the open-chain aldohexose and two orientations of L-gulonic acid and D-xylulose are shown. P = phosphate.
UDP-glucuronic acid is a sugar used in the creation of polysaccharides and is an intermediate in the biosynthesis of ascorbic acid (except in primates and guinea pigs ). It also participates in the heme degradation process of human. It is made from UDP-glucose by UDP-glucose 6-dehydrogenase (EC 1.1.1.22) using NAD+ as a cofactor.
- C₁₅H₂₂N₂O₁₈P₂
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- 580.285
- CHEBI:17200
USA.gov. D-Glucuronic Acid | C6H10O7 | CID 94715 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Glucuronic acid. Molecular Formula CHO. Average mass 194.139 Da. Monoisotopic mass 194.042648 Da. ChemSpider ID 58552. - 4 of 4 defined stereocentres.
