1-Feruloyl-D-glucose (BioDeep_00001867583)

Main id: BioDeep_00000001024

 

PANOMIX_OTCML-2023


Metabolite Card


(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl 3-(4-hydroxy-3-methoxyphenyl)acrylate

  Formula: C16H20O9 (356.1107)
Chinese Names: 1-O-香兰酰-D-葡萄糖
  Spectrum Hits: Top Source () %

Molecular Structure

SMILES: COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O
InChI: InChI=1S/C16H20O9/c1-23-10-6-8(2-4-9(10)18)3-5-12(19)25-16-15(22)14(21)13(20)11(7-17)24-16/h2-6,11,13-18,20-22H,7H2,1H3/b5-3+/t11-,13-,14+,15-,16+/m1/s1


Description

1-O-feruloyl-beta-D-glucose is a beta-D-glucoside resulting from the formal condensation of the carboxy group of ferulic acid with the anomeric hydroxy group of beta-D-glucose. It has a role as an antioxidant and a plant metabolite. It is a beta-D-glucoside, a cinnamate ester, a member of phenols and an aromatic ether. It is functionally related to a ferulic acid.
1-O-feruloyl-beta-D-glucose is a natural product found in Balanophora japonica, Linaria japonica, and other organisms with data available.
A beta-D-glucoside resulting from the formal condensation of the carboxy group of ferulic acid with the anomeric hydroxy group of beta-D-glucose.

Synonyms

22 synonym names

(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl 3-(4-hydroxy-3-methoxyphenyl)acrylate; [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate; 1-O-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-beta-D-glucopyranose; 1-[3-(4-Hydroxy-3-Methoxyphenyl)-2-propenoate] beta-D-Glucopyranose; 1-[3-(4-Hydroxy-3-Methoxyphenyl)-2-propenoate] ss-D-Glucopyranose; (E)-4-hydroxy-3-methoxycinnamoyl-beta-D-glucopyranose; 1-O-trans-feruloyl-beta-D-glucopyranoside; ferulic acid beta-D-glucopyranosyl ester; 1-O-(E)-p-feruloyl-beta-D-glucopyranose; trans-p-Feruloyl beta-D-glucopyranoside; trans-p-feruloyl-beta-D-glucopyranoside; (E)-1-O-feruloyl-beta-D-glucopyranose; Ferulic Acid Acyl-beta-D-glucoside; 1-O-[(E)-feruloyl]-beta-D-glucose; Ferulic acid acyl-|A-D-glucoside; Ferulic acid acyl-??-D-glucoside; Ferulic acid acyl-β-D-glucoside; 1-O-(E)-feruloyl-beta-D-glucose; 1-O-feruloyl-beta-D-glucoside; 1-O-feruloyl-beta-D-glucose; 1-O-feruloyl-beta-glucose; 1-Feruloyl-D-glucose



Cross Reference

11 cross reference id

Classification Terms

Related Pathways

Reactome()

BioCyc(1)

PlantCyc(1)

Biological Process

3 related biological process reactions.

Reactome()

BioCyc()

WikiPathways()

Plant Reactome()

INOH()

PlantCyc()

COVID-19 Disease Map()

PathBank()

PharmGKB()

24 organism taxonomy source information

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。



Literature Reference

  • Mun Seok Jo, Seoyoung Lee, Jae Sik Yu, Su Cheol Baek, Young-Chang Cho, Ki Hyun Kim. Megastigmane Derivatives from the Cladodes of Opuntia humifusa and Their Nitric Oxide Inhibitory Activities in Macrophages. Journal of natural products. 2020 03; 83(3):684-692. doi: 10.1021/acs.jnatprod.9b01120. [PMID: 32118424]
  • Su Yang Jeong, Do Youn Jun, Young Ho Kim, Byung-Sun Min, Bo Kyung Min, Mi Hee Woo. Monoterpenoids from the aerial parts of Aruncus dioicus var. kamtschaticus and their antioxidant and cytotoxic activities. Bioorganic & medicinal chemistry letters. 2011 Jun; 21(11):3252-6. doi: 10.1016/j.bmcl.2011.04.043. [PMID: 21546250]
  • . . . . doi: . [PMID: 20971893]