Quercetin 3-lathyroside (BioDeep_00000001029)

 

Secondary id: BioDeep_00000270658, BioDeep_00000403100, BioDeep_00000870438, BioDeep_00001867584

human metabolite PANOMIX_OTCML-2023


代谢物信息卡片


3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxytetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-chromen-4-one

化学式: C26H28O16 (596.1377)
中文名称: 槲皮素3-桑布双糖苷
谱图信息: 最多检出来源 Viridiplantae(plant) 15.36%

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](CO1)O)O)O)c1ccc(c(c1)O)O)O)O
InChI: InChI=1S/C26H28O16/c27-6-15-18(34)20(36)24(42-25-21(37)17(33)13(32)7-38-25)26(40-15)41-23-19(35)16-12(31)4-9(28)5-14(16)39-22(23)8-1-2-10(29)11(30)3-8/h1-5,13,15,17-18,20-21,24-34,36-37H,6-7H2/t13-,15-,17+,18-,20+,21-,24-,25+,26+/m1/s1

描述信息

Quercetin 3-O-[beta-D-xylosyl-(1->2)-beta-D-glucoside] is a quercetin O-glucoside that is quercetin attached to a beta-D-sambubiosyl residue at position 3 via a glycosidc linkage. It has a role as an antioxidant and a plant metabolite. It is a quercetin O-glucoside, a disaccharide derivative and a tetrahydroxyflavone.
Quercetin 3-sambubioside is a natural product found in Lathyrus chloranthus, Euphorbia prostrata, and other organisms with data available.
Isolated from horseradish (Armoracia rusticana) leaves. Quercetin 3-lathyroside is found in horseradish and brassicas.
Quercetin 3-sambubioside is found in fruits. Quercetin 3-sambubioside is isolated from Actinidia arguta (tara vine).

同义名列表

15 个代谢物同义名

3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxytetrahydropyran-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-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one; 3-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one; 3-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2-O-|A-D-xylopyranosyl-|A-D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 2-O-beta-D-xylopyranosyl-beta-D-glucopyranoside; quercetin 3-O-beta-xylopyranosyl-(1-2)-O-beta-glucopyranoside; Quercetin 3-O-[beta-D-xylosyl-(1->2)-beta-D-glucoside]; (+)-Quercetin 3-O-sambubioside; Quercetin 3-O-sambubioside; Quercetin 3-sambubioside; Quercetin 3-lathyroside; AC1NUPP6



数据库引用编号

20 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

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)

16 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

  • Xin Li, Lipeng Yang, Shaoyang Liu, Dongqing Fei, Min Zhang, Yuxian Zhang. Effect of quercetin-3-O-sambubioside isolated from Eucommia ulmoides male flowers on spontaneous activity and convulsion rate in mice. Planta medica. 2014 Aug; 80(12):974-7. doi: 10.1055/s-0034-1382902. [PMID: 25098932]
  • Monika A Olszewska, Anna Kwapisz. Metabolite profiling and antioxidant activity of Prunus padus L. flowers and leaves. Natural product research. 2011 Jul; 25(12):1115-31. doi: 10.1080/14786410903230359. [PMID: 21347973]
  • Li-Wen Tian, Ying-Jun Zhang, Chang Qu, Yi-Fei Wang, Chong-Ren Yang. Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni. Journal of natural products. 2010 Feb; 73(2):160-3. doi: 10.1021/np900530n. [PMID: 20092288]
  • Guang-Bo Xie, Feng Niu, Xiao-Jing Wang, Lian-Di Lei, Peng-Fei Tu. Chemical constituents from the leaves of Ilex pernyi. Yao xue xue bao = Acta pharmaceutica Sinica. 2008 Jan; 43(1):60-2. doi: . [PMID: 18357733]
  • Subeki Subeki, Hideyuki Matsuura, Kosaku Takahashi, Masahiro Yamasaki, Osamu Yamato, Yoshimitsu Maede, Ken Katakura, Sumiko Kobayashi, Trimurningsih Trimurningsih, Chairul Chairul, Teruhiko Yoshihara. Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri. Journal of natural products. 2005 Apr; 68(4):537-9. doi: 10.1021/np0497245. [PMID: 15844943]
  • Feng Wei, Shuang-Cheng Ma, Lin-Yun Ma, Paul Pui-Hay But, Rui-Chao Lin, Ikhlas A Khan. Antiviral flavonoids from the seeds of Aesculus chinensis. Journal of natural products. 2004 Apr; 67(4):650-3. doi: 10.1021/np030470h. [PMID: 15104496]