trans-p-Feruloyl-beta-D-glucopyranoside (BioDeep_00000001024)

 

Secondary id: BioDeep_00000017728, BioDeep_00000019118, BioDeep_00000227127, BioDeep_00000234543, BioDeep_00000620824, BioDeep_00000871783, BioDeep_00001867583

human metabolite PANOMIX_OTCML-2023


代谢物信息卡片


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

化学式: C16H20O9 (356.110727)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 0.49%

分子结构信息

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

描述信息

Trans-p-feruloyl-beta-d-glucopyranoside, also known as 1-feruloyl-D-glucose, is a member of the class of compounds known as hydroxycinnamic acid glycosides. Hydroxycinnamic acid glycosides are glycosylated hydoxycinnamic acids derivatives. Trans-p-feruloyl-beta-d-glucopyranoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Trans-p-feruloyl-beta-d-glucopyranoside can be found in a number of food items such as green bell pepper, pepper (c. annuum), yellow bell pepper, and orange bell pepper, which makes trans-p-feruloyl-beta-d-glucopyranoside a potential biomarker for the consumption of these food products.
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.
Lavandoside is an active compound found from Lavandula spica flowers[1].

同义名列表

49 个代谢物同义名

(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; (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2E)-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; (e)-4-Hydroxy-3-methoxycinnamoyl-β-D-glucopyranose; (e)-4-Hydroxy-3-methoxycinnamoyl-b-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; 1-O-trans-Feruloyl-β-D-glucopyranoside; 1-O-trans-Feruloyl-b-D-glucopyranoside; Ferulic acid b-D-glucopyranosyl ester; (E)-1-O-feruloyl-beta-D-glucopyranose; Ferulic acid β-D-glucopyranosyl ester; 1-O-(e)-p-Feruloyl-β-D-glucopyranose; trans-p-Feruloyl-β-D-glucopyranoside; Ferulate beta-D-glucopyranosyl ester; 1-O-(e)-p-Feruloyl-b-D-glucopyranose; trans-p-Feruloyl-b-D-glucopyranoside; 1-O-(trans-Feruloyl)-beta-D-glucose; (e)-1-O-Feruloyl-b-D-glucopyranose; Ferulic Acid Acyl-beta-D-glucoside; (e)-1-O-Feruloyl-β-D-glucopyranose; Ferulate β-D-glucopyranosyl ester; 1-O-[(E)-feruloyl]-beta-D-glucose; Ferulate b-D-glucopyranosyl ester; 1-O-(trans-Feruloyl)-β-D-glucose; Ferulic acid acyl-|A-D-glucoside; 1-O-(trans-Feruloyl)-b-D-glucose; Ferulic acid acyl-??-D-glucoside; Ferulic acid acyl-β-D-glucoside; 1-O-(E)-feruloyl-beta-D-glucose; 1-O-[(e)-Feruloyl]-b-D-glucose; 1-O-[(e)-Feruloyl]-β-D-glucose; 1-O-Feruloyl-β-D-glucose; 1-O-feruloyl-beta-D-glucoside; 1-O-(e)-Feruloyl-β-D-glucose; 1-O-(e)-Feruloyl-b-D-glucose; 1-O-feruloyl-beta-D-glucose; 1-O-feruloyl-beta-glucose; 1-O-Feruloyl-b-D-glucose; 1-O-Feruloyl-β-D-glucose; 1-Feruloyl-D-glucose; Lavandoside



数据库引用编号

19 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

121 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(8)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(113)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

26 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

  • 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]