Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H10O7 |
| Molecular Weight | 194.1394 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O
InChI
InChIKey=AEMOLEFTQBMNLQ-WAXACMCWSA-N
InChI=1S/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6-/m0/s1
DescriptionCurator's Comment: Description was created based on several sources, including
http://www.hmdb.ca/metabolites/hmdb00127 and https://www.ncbi.nlm.nih.gov/mesh/68020723
Curator's Comment: Description was created based on several sources, including
http://www.hmdb.ca/metabolites/hmdb00127 and https://www.ncbi.nlm.nih.gov/mesh/68020723
Glucuronic acid (α-D-GLUCURONIC ACID) is a carboxylic acid that has the structure of a glucose molecule that has had its sixth carbon atom (of six total) oxidized. The salts of glucuronic acid are known as glucuronates. Glucuronic acid is highly soluble in water. In humans, glucuronic acid is often linked to toxic or poisonous substances to allow for subsequent elimination, and to hormones to allow for easier transport. These linkages involve O-glycosidic bonds. The process is known as glucuronidation, and the resulting substances are known as glucuronides (or glucuronosides). Glucuronidation uses UDP-glucuronic acid (glucuronic acid linked via a glycosidic bond to uridine diphosphate) as an intermediate. UDP-glucuronic acid is formed in the liver of all animals. α-D-GLUCURONIC ACID is used as pharmaceutical intermediate and in chemical research.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inactivation of Corynebacterium glutamicum NCgl0452 and the role of MgtA in the biosynthesis of a novel mannosylated glycolipid involved in lipomannan biosynthesis. | 2007 Feb 16 |
|
| A sulfated glucuronofucan containing both fucofuranose and fucopyranose residues from the brown alga Chordaria flagelliformis. | 2008 Oct 13 |
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444791
Created by
admin on Sat Dec 16 10:00:48 GMT 2023 , Edited by admin on Sat Dec 16 10:00:48 GMT 2023
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M7Y086VB5G
Created by
admin on Sat Dec 16 10:00:48 GMT 2023 , Edited by admin on Sat Dec 16 10:00:48 GMT 2023
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DTXSID201036416
Created by
admin on Sat Dec 16 10:00:48 GMT 2023 , Edited by admin on Sat Dec 16 10:00:48 GMT 2023
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70021-34-0
Created by
admin on Sat Dec 16 10:00:48 GMT 2023 , Edited by admin on Sat Dec 16 10:00:48 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
