Rhamnosylvitexin (BioDeep_00000230450)

Main id: BioDeep_00000003344

 

PANOMIX_OTCML-2023


代谢物信息卡片


8-((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

化学式: C27H30O14 (578.163548)
中文名称: 牡荆素鼠李糖苷, 牡荆素-2-O-鼠李糖苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=C([C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O[C@H]2[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O2)O)O)CO)C2OC(C3C=CC(O)=CC=3)=CC(=O)C=2C(O)=C1
InChI: InChI=1S/C27H30O14/c1-9-19(33)21(35)23(37)27(38-9)41-26-22(36)20(34)16(8-28)40-25(26)18-13(31)6-12(30)17-14(32)7-15(39-24(17)18)10-2-4-11(29)5-3-10/h2-7,9,16,19-23,25-31,33-37H,8H2,1H3/t9-,16+,19-,20+,21+,22-,23+,25-,26+,27-/m0/s1

描述信息

Vitexin 2-O-alpha-L-rhamnoside is a derivative of vitexin having an alpha-L-rhamnosyl residue attached at the 2-position of the glucitol moiety. It has a role as a plant metabolite. It is a C-glycosyl compound, a trihydroxyflavone and a disaccharide derivative. It is functionally related to a vitexin. It is a conjugate acid of a vitexin 2-O-alpha-L-rhamnoside(1-).
Vitexin 2-O-rhamnoside is a natural product found in Crataegus monogyna, Passiflora coactilis, and other organisms with data available.
See also: Crataegus monogyna flowering top (part of).
Vitexin-2"-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].
Vitexin-2"-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].

同义名列表

27 个代谢物同义名

8-((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one; 8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one; 8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one; (1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol; (1S)-1,5-anhydro-2-O-(alpha-L-rhamnopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol; Vitexin 2-O-rhamnoside, primary pharmaceutical reference standard; VITEXIN-2-O-RHAMNOSIDE (CONSTITUENT OF HAWTHORN LEAF WITH FLOWER); vitexin-2invertedexclamationmarka-o-rhamnoside; Vitexin 2-O-rhamnoside, analytical standard; Apigenin-8-C-glucoside-2-rhamnoside; vitexin 2-O-alpha-L-rhamnoside; 2-O-RHAMNOPYRANOSYLVITEXIN; Vitexin-2"-O-rhamnoside; Vitexin 2"-O-rhamnoside; Vitexin 2-O-rhamnoside; Vitexin-2-O-rhamnoside; vitexin-2-O-rhamnoside; 2-O-Rhamnosylvitexin; Vitexin 2-rhamnoside; Vitexin-2-rhamnoside; 2-Rhamnosylvitexin; Rhamnosylvitexin; UNII-UD7Y63I5X5; MEGxp0_001018; ACon1_001257; UD7Y63I5X5; Vitexin-2"-O-rhamnoside



数据库引用编号

8 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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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)

19 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

  • Xu Pang, Mei Wang, Shuang-Yan Wang, Jie Zhang, Ya-Peng Du, Ye Zhao, Xiao-Hui Zheng, Bai-Ping Ma. Phenolic compounds from the leaves of Crataegus pinnatifida Bge. var. major N.E.Br. And their lipid-lowering effects. Bioorganic & medicinal chemistry letters. 2021 09; 47(?):128211. doi: 10.1016/j.bmcl.2021.128211. [PMID: 34157392]
  • Jensen A Lund, Paula N Brown, Paul R Shipley. Quantification of North American and European Crataegus flavonoids by nuclear magnetic resonance spectrometry. Fitoterapia. 2020 Jun; 143(?):104537. doi: 10.1016/j.fitote.2020.104537. [PMID: 32145312]
  • Soo Yee Lee, Ahmed Mediani, Maulidiani Maulidiani, Alfi Khatib, Intan Safinar Ismail, Norhasnida Zawawi, Faridah Abas. Comparison of partial least squares and random forests for evaluating relationship between phenolics and bioactivities of Neptunia oleracea. Journal of the science of food and agriculture. 2018 Jan; 98(1):240-252. doi: 10.1002/jsfa.8462. [PMID: 28580581]
  • Paolino Ninfali, Elena Antonini, Alessandra Frati, Emanuele-Salvatore Scarpa. C-Glycosyl Flavonoids from Beta vulgaris Cicla and Betalains from Beta vulgaris rubra: Antioxidant, Anticancer and Antiinflammatory Activities-A Review. Phytotherapy research : PTR. 2017 Jun; 31(6):871-884. doi: 10.1002/ptr.5819. [PMID: 28464411]
  • Paolino Ninfali, Sabrina Dominici, Donato Angelino, Lorenzo Gennari, Costantina Buondelmonte, Luca Giorgi. An enzyme-linked immunosorbent assay for the measurement of plasma flavonoids in mice fed apigenin-C-glycoside. Journal of the science of food and agriculture. 2013 Sep; 93(12):3087-93. doi: 10.1002/jsfa.6143. [PMID: 23526334]
  • S Vargas, K Ndjoko Ioset, A-E Hay, J-R Ioset, S Wittlin, K Hostettmann. Screening medicinal plants for the detection of novel antimalarial products applying the inhibition of β-hematin formation. Journal of pharmaceutical and biomedical analysis. 2011 Dec; 56(5):880-6. doi: 10.1016/j.jpba.2011.06.026. [PMID: 21872416]