Quosp (BioDeep_00000230515)

Main id: BioDeep_00000003663

 

PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


3-[[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-2-tetrahydropyranyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-chromenone

化学式: C27H30O17 (626.148293)
中文名称: 槲皮素3-O-槐糖, 白麻苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c1(cc(c2c(c1)oc(c(c2=O)O[C@H]1[C@@H]([C@@H]([C@@H]([C@@H](O1)CO)O)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)c1ccc(c(c1)O)O)O)O
InChI: InChI=1S/C27H30O17/c28-6-14-17(34)20(37)22(39)26(41-14)44-25-21(38)18(35)15(7-29)42-27(25)43-24-19(36)16-12(33)4-9(30)5-13(16)40-23(24)8-1-2-10(31)11(32)3-8/h1-5,14-15,17-18,20-22,25-35,37-39H,6-7H2/t14-,15+,17-,18-,20+,21-,22-,25-,26+,27+/m1/s1

描述信息

Quercetin 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside is a quercetin O-glucoside that is quercetin attached to a beta-D-sophorosyl residue at position 3 via a glycosidic linkage. It has a role as an antioxidant and a plant metabolite. It is a tetrahydroxyflavone and a sophoroside. It is a conjugate acid of a quercetin 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside(1-).
Quosp is a natural product found in Ranunculus hederaceus, Equisetum bogotense, and other organisms with data available.
A quercetin O-glucoside that is quercetin attached to a beta-D-sophorosyl residue at position 3 via a glycosidic linkage.
Baimaside (Quercetin 3-O-sophoroside) is isolated from the flowers of A. venetum, is a scavenger of superoxide anions[1].
Baimaside (Quercetin 3-O-sophoroside) is isolated from the flowers of A. venetum, is a scavenger of superoxide anions[1].

同义名列表

24 个代谢物同义名

3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-5,7-dihydroxy-; 2-(3,4-dihydroxyphenyl)-3-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 2-O-hexopyranosylhexopyranoside; Quercetin 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside; Quercetin, 3-(O-glucosylglucoside); Quercetin 3-beta-D-sophoroside; Quercetin 3-O-sophoroside; quercetin-3-O-sophoroside; Quercetin 3-glucobioside; QUERCETIN-3-SOPHOROSIDE; quercetin 3-O-beta-D-; quercetin diglucoside; Baimaside; Quosp; 3-[[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-2-tetrahydropyranyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-chromenone; 3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-chromen-4-one; 3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-methylol-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-chromone; 3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-oxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-chromen-4-one; 27459-71-8; 18609-17-1; C12667; Quercetin 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside



数据库引用编号

16 个数据库交叉引用编号

分类词条

相关代谢途径

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PlantCyc(1)

代谢反应

0 个相关的代谢反应过程信息。

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BioCyc(0)

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Plant Reactome(0)

INOH(0)

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158 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

  • Javad Mottaghipisheh, Mohammad Mahmoodi Sourestani, Tivadar Kiss, Attila Horváth, Barbara Tóth, Mehdi Ayanmanesh, Amin Khamushi, Dezső Csupor. Comprehensive chemotaxonomic analysis of saffron crocus tepal and stamen samples, as raw materials with potential antidepressant activity. Journal of pharmaceutical and biomedical analysis. 2020 May; 184(?):113183. doi: 10.1016/j.jpba.2020.113183. [PMID: 32105944]
  • Yanling Wang, Mark A Berhow, Molly Black, Elizabeth H Jeffery. A comparison of the absorption and metabolism of the major quercetin in brassica, quercetin-3-O-sophoroside, to that of quercetin aglycone, in rats. Food chemistry. 2020 May; 311(?):125880. doi: 10.1016/j.foodchem.2019.125880. [PMID: 31771913]
  • Hongjuan Li, Ying Liu, Yuetao Yi, Qin Miao, Sujing Liu, Feng Zhao, Wei Cong, Chunhua Wang, Chuanhai Xia. Purification of quercetin-3-O-sophoroside and isoquercitrin from Poacynum hendersonii leaves using macroporous resins followed by Sephadex LH-20 column chromatography. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2017 Mar; 1048(?):56-63. doi: 10.1016/j.jchromb.2017.01.041. [PMID: 28213296]
  • Ning Li, Ying Wang, Xuezheng Li, Hong Zhang, Di Zhou, Wenli Wang, Wei Li, Xiangrong Zhang, Xinyu Li, Yue Hou, Dali Meng. Bioactive phenols as potential neuroinflammation inhibitors from the leaves of Xanthoceras sorbifolia Bunge. Bioorganic & medicinal chemistry letters. 2016 10; 26(20):5018-5023. doi: 10.1016/j.bmcl.2016.08.094. [PMID: 27623545]
  • Jun Zhou, Jiang Bing Sun, Xin Yu Xu, Zhao Hui Cheng, Ping Zeng, Feng Qiao Wang, Qiong Zhang. Application of mixed cloud point extraction for the analysis of six flavonoids in Apocynum venetum leaf samples by high performance liquid chromatography. Journal of pharmaceutical and biomedical analysis. 2015 Mar; 107(?):273-9. doi: 10.1016/j.jpba.2015.01.003. [PMID: 25625477]
  • Christian Seutter von Loetzen, Thessa Jacob, Olivia Hartl-Spiegelhauer, Lothar Vogel, Dirk Schiller, Cornelia Spörlein-Güttler, Rainer Schobert, Stefan Vieths, Maximilian Johannes Hartl, Paul Rösch. Ligand Recognition of the Major Birch Pollen Allergen Bet v 1 is Isoform Dependent. PloS one. 2015; 10(6):e0128677. doi: 10.1371/journal.pone.0128677. [PMID: 26042900]
  • Christian Seutter von Loetzen, Thomas Hoffmann, Maximilian J Hartl, Kristian Schweimer, Wilfried Schwab, Paul Rösch, Olivia Hartl-Spiegelhauer. Secret of the major birch pollen allergen Bet v 1: identification of the physiological ligand. The Biochemical journal. 2014 Feb; 457(3):379-90. doi: 10.1042/bj20130413. [PMID: 24171862]
  • Almudena Trapero, Oussama Ahrazem, Angela Rubio-Moraga, Maria Luisa Jimeno, Maria Dolores Gómez, Lourdes Gómez-Gómez. Characterization of a glucosyltransferase enzyme involved in the formation of kaempferol and quercetin sophorosides in Crocus sativus. Plant physiology. 2012 Aug; 159(4):1335-54. doi: 10.1104/pp.112.198069. [PMID: 22649274]