D-Glucuronic acid (BioDeep_00000400046)

Main id: BioDeep_00000001733

Secondary id: BioDeep_00000003270

natural product PANOMIX_OTCML-2023


代谢物信息卡片


aldehydo-D-glucuronic acid

化学式: C6H10O7 (194.042651)
中文名称: D-葡萄糖醛酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(C(C(OC(C1O)O)C(=O)O)O)O
InChI: InChI=1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h1-5,8-11H,(H,12,13)/t2-,3+,4-,5-/m0/s1

描述信息

A D-glucuronic acid in cyclic pyranose form.
D-glucuronic acid, also known as glucuronate or glucuronic acid, monopotassium salt, belongs to glucuronic acid derivatives class of compounds. Those are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. D-glucuronic acid is soluble (in water) and a weakly acidic compound (based on its pKa). D-glucuronic acid can be found in a number of food items such as peach, dandelion, corn, and horseradish tree, which makes D-glucuronic acid a potential biomarker for the consumption of these food products. Glucuronic acid (from Ancient Greek γλυκύς "sweet" + οὖρον "urine") is a uronic acid that was first isolated from urine (hence the name). It is found in many gums such as gum arabic (c. 18\\\\%) and xanthan, and is important for the metabolism of microorganisms, plants and animals .
D-Glucuronic acid is an important intermediate isolated from many gums. D-Glucuronic acid and its derivative glucuronolactone are as a liver antidote in the prophylaxis of human health. D-Glucuronic acid has an anti-inflammatory effect for the skin[1].
D-Glucuronic acid is an important intermediate isolated from many gums. D-Glucuronic acid and its derivative glucuronolactone are as a liver antidote in the prophylaxis of human health. D-Glucuronic acid has an anti-inflammatory effect for the skin[1].

同义名列表

5 个代谢物同义名

aldehydo-D-glucuronic acid; α-D-Glucopyranuronic acid; beta-D-glucuronic acid; D-Glucuronic acid; D-Glucopyranuronic acid



数据库引用编号

31 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(7)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

25 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。



文献列表

  • Pengyun Wang, Baolong Zhao, Zhongtian Yin, Xin Gao, Mengyao Liu. Structure elucidation and anticancer activity of a heteropolysaccharide from white tea. Carbohydrate polymers. 2024 Jun; 333(?):121976. doi: 10.1016/j.carbpol.2024.121976. [PMID: 38494228]
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  • Duangjai Tungmunnithum, Samantha Drouet, Christophe Hano. Flavonoids from Sacred Lotus Stamen Extract Slows Chronological Aging in Yeast Model by Reducing Oxidative Stress and Maintaining Cellular Metabolism. Cells. 2022 02; 11(4):. doi: 10.3390/cells11040599. [PMID: 35203251]
  • Ping Zhou, Jing Zhang, Yudi Xu, Peng Zhang, Yongqing Xiao, Ying Liu. Simultaneous quantification of anthraquinone glycosides, aglycones, and glucuronic acid metabolites in rat plasma and tissues after oral administration of raw and steamed rhubarb in blood stasis rats by UHPLC-MS/MS. Journal of separation science. 2022 Jan; 45(2):529-541. doi: 10.1002/jssc.202100623. [PMID: 34784448]
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  • Wenxiang Xiao, Jing Liu, Yinan Xiong, Yaoxin Li, Hua Li. Fluorescent sensing of free bilirubin at nanomolar level using a Langmuir-Blodgett film of glucuronic acid-functionalized gold nanoclusters. Analytical and bioanalytical chemistry. 2021 Nov; 413(28):7009-7019. doi: 10.1007/s00216-021-03660-6. [PMID: 34535815]
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