Resveratroloside (BioDeep_00000396677)

Main id: BioDeep_00000021668

 

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


(2S,3R,4S,5S,6R)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

化学式: C20H22O8 (390.1315)
中文名称: 白藜芦醇甙
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O
InChI: InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1

描述信息

Resveratroloside is a natural product found in Vitis vinifera, Pinus sylvestris, and other organisms with data available.

同义名列表

34 个代谢物同义名

2-{4-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol; 3,4',5-Trihydroxystilbene 4'-O-beta-D-glucopyranoside; (Z)-Resveratrol 4'-glucoside; Resveratrol 4'-O-glucoside; Resveratrol 4-beta-D-glucoside; Resveratrol 4'-glucoside; Resveratrol 4-glucoside; Resveratroloside; (2S,3R,4S,5S,6R)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-(4-((E)-3,5-Dihydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; .BETA.-D-GLUCOPYRANOSIDE, 4-(2-(3,5-DIHYDROXYPHENYL)ETHENYL)PHENYL, (E)-; .BETA.-D-GLUCOPYRANOSIDE, 4-((1E)-2-(3,5-DIHYDROXYPHENYL)ETHENYL)PHENYL; beta-D-Glucopyranoside, 4-(2-(3,5-dihydroxyphenyl)ethenyl)phenyl, (E)-; 4-((1E)-2-(3,5-DIHYDROXYPHENYL)ETHENYL)PHENYL .BETA.-D-GLUCOPYRANOSIDE; beta-D-Glucopyranoside, 4-((1E)-2-(3,5-dihydroxyphenyl)ethenyl)phenyl; 4-((1E)-2-(3,5-Dihydroxyphenyl)ethenyl)phenyl beta-D-glucopyranoside; B-D-glucopyranoside, 4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenyl; 4-(2-(3,5-Dihydroxyphenyl)ethenyl)phenyl beta-D-glucopyranoside; 4-[2-(3,5-Dihydroxyphenyl)ethenyl]phenyl beta-D-glucopyranoside; 3,4,5-TRIHYDROXYSTILBENE 4-MONO-.BETA.-D-GLYCOPYRANOSIDE; 3,4,5-Trihydroxystilbene 4-mono-beta-D-glycopyranoside; 3,5,4-trihydroxystilbene-4-O-beta-D-glucoside; trans-resveratrol-4-O-beta-d-glucopyranoside; trans-Resveratrol 4-O-b-D-glucopyranoside; RESVERATROL 4-O-.BETA.-D-GLUCOPYRANOSIDE; Trans-Resveratrol 4-O-beta-D-glucuronide; Resveratrol 4-o-beta-D-glucopyranoside; 3,5,4-trihydroxystilbene-4-O-glucoside; Resveratrol (3,4,5-trihydroxystilbene); E.resveratroloside; UNII-7DBS6RKM2S; 7DBS6RKM2S; GOB C



数据库引用编号

9 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)

55 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。

亚细胞结构定位 关联基因列表


文献列表

  • Bettina Rainer, Silvia Revoltella, Fabian Mayr, Julia Moesslacher, Valentina Scalfari, Roland Kohl, Birgit Waltenberger, Konrad Pagitz, Bianka Siewert, Stefan Schwaiger, Hermann Stuppner. From bench to counter: Discovery and validation of a peony extract as tyrosinase inhibiting cosmeceutical. European journal of medicinal chemistry. 2019 Dec; 184(?):111738. doi: 10.1016/j.ejmech.2019.111738. [PMID: 31655335]
  • Xiaohui Zhao, Jihong Tao, Ting Zhang, Sirong Jiang, Wei Wei, Hongping Han, Yun Shao, Guoyin Zhou, Huilan Yue. Resveratroloside Alleviates Postprandial Hyperglycemia in Diabetic Mice by Competitively Inhibiting α-Glucosidase. Journal of agricultural and food chemistry. 2019 Mar; 67(10):2886-2893. doi: 10.1021/acs.jafc.9b00455. [PMID: 30785285]
  • B A Dar, S H Lone, W A Shah, K A Bhat. LC-MS Guided Isolation of Bioactive Principles from Iris hookeriana and Bioevaluation of Isolates for Antimicrobial and Antioxidant Activities. Drug research. 2016 Aug; 66(8):427-31. doi: 10.1055/s-0042-108337. [PMID: 27281447]
  • Muhammad Usman Mirza, A Hammad Mirza, Noor-Ul-Huda Ghori, Saba Ferdous. Glycyrrhetinic acid and E.resveratroloside act as potential plant derived compounds against dopamine receptor D3 for Parkinson's disease: a pharmacoinformatics study. Drug design, development and therapy. 2015; 9(?):187-98. doi: 10.2147/dddt.s72794. [PMID: 25565772]
  • Mar Larrosa, Joao Tomé-Carneiro, María J Yáñez-Gascón, David Alcántara, María V Selma, David Beltrán, María T García-Conesa, Cristina Urbán, Ricardo Lucas, Francisco Tomás-Barberán, Juan C Morales, Juan Carlos Espín. Preventive oral treatment with resveratrol pro-prodrugs drastically reduce colon inflammation in rodents. Journal of medicinal chemistry. 2010 Oct; 53(20):7365-76. doi: 10.1021/jm1007006. [PMID: 20866032]
  • Isabel Rivero-Cruz, Laura Acevedo, José A Guerrero, Sergio Martínez, Robert Bye, Rogelio Pereda-Miranda, Scott Franzblau, Barbara N Timmermann, Rachel Mata. Antimycobacterial agents from selected Mexican medicinal plants. The Journal of pharmacy and pharmacology. 2005 Sep; 57(9):1117-26. doi: 10.1211/jpp.57.9.0007. [PMID: 16105233]
  • B C Vastano, Y Chen, N Zhu, C T Ho, Z Zhou, R T Rosen. Isolation and identification of stilbenes in two varieties of Polygonum cuspidatum. Journal of agricultural and food chemistry. 2000 Feb; 48(2):253-6. doi: 10.1021/jf9909196. [PMID: 10691624]
  • G S Jayatilake, H Jayasuriya, E S Lee, N M Koonchanok, R L Geahlen, C L Ashendel, J L McLaughlin, C J Chang. Kinase inhibitors from Polygonum cuspidatum. Journal of natural products. 1993 Oct; 56(10):1805-10. doi: 10.1021/np50100a021. [PMID: 8277318]