Sinapaldehyde glucoside (BioDeep_00000279351)

 

Secondary id: BioDeep_00001894464

natural product


代谢物信息卡片


(E)-3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enal

化学式: C17H22O9 (370.1263762)
中文名称: 芥子醛配糖物
谱图信息: 最多检出来源 Viridiplantae(plant) 2.8%

Reviewed

Last reviewed on 2024-07-12.

Cite this Page

Sinapaldehyde glucoside. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/sinapaldehyde_glucoside (retrieved 2024-09-20) (BioDeep RN: BioDeep_00000279351). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: COC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(=CC(=C1)\C=C\C=O)OC
InChI: InChI=1S/C17H22O9/c1-23-10-6-9(4-3-5-18)7-11(24-2)16(10)26-17-15(22)14(21)13(20)12(8-19)25-17/h3-7,12-15,17,19-22H,8H2,1-2H3/b4-3+/t12-,13-,14+,15-,17+/m1/s1

描述信息

(E)-sinapaldehyde 4-O-beta-D-glucopyranoside is a beta-D-glucoside resulting from the formal condensation of the phenolic hydroxy group of (E)-sinapaldehyde with beta-D-glucose. It has a role as a plant metabolite. It is a beta-D-glucoside, a monosaccharide derivative, a dimethoxybenzene and a member of cinnamaldehydes. It is functionally related to an (E)-sinapaldehyde.

Sinapaldehyde glucoside is a natural compound belonging to the phenolic glucoside class. It is formed by the condensation of sinapaldehyde, a type of phenolic aldehyde, with a glucose molecule through a glycosidic bond. This compound is commonly found in plants, particularly in the seeds of Brassica species, which include crops like mustard and rapeseed.
Chemically, sinapaldehyde glucoside is characterized by the presence of a sinapaldehyde moiety, which consists of a benzene ring with hydroxyl groups at the para and meta positions, and an aldehyde group at the ortho position relative to one of the hydroxyl groups. The glucose moiety is attached to the aldehyde group of sinapaldehyde via a beta-glycosidic linkage.
In terms of its properties, sinapaldehyde glucoside is typically a solid or crystalline substance with a specific melting point. It is soluble in water and polar organic solvents, reflecting its hydrophilic nature due to the presence of the glucose moiety. The compound may exhibit various biological activities, including antioxidant, anti-inflammatory, and antimicrobial effects, which are attributed to the phenolic groups present in the sinapaldehyde moiety.
Sinapaldehyde glucoside has been studied for its potential health benefits and is considered a bioactive compound in the context of dietary phytochemicals. Its presence in plant-based foods contributes to the overall health-promoting effects associated with the consumption of Brassica vegetables and related products.


(2E)-3-[4-(β-D-Glucopyranosyloxy)-3,5-dimethoxyphenyl]-2-propenal. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=154461-65-1 (retrieved 2024-07-12) (CAS RN: 154461-65-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

同义名列表

2 个代谢物同义名

Sinapaldehyde glucoside; NCGC00385983-01_C17H22O9_2,6-Dimethoxy-4-[(1E)-3-oxo-1-propen-1-yl]phenyl beta-D-glucopyranoside



数据库引用编号

10 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

代谢反应

45 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(44)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 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

  • Ui-Joung Youn, Quan Cheng Chen, Wen-Yi Jin, Ik-Soo Lee, Hong-Jin Kim, Jong-Pill Lee, Min-Jung Chang, Byung-Sun Min, Ki-Hwan Bae. Cytotoxic lignans from the stem bark of Magnolia officinalis. Journal of natural products. 2007 Oct; 70(10):1687-9. doi: 10.1021/np070388c. [PMID: 17918910]