5-Styrylresorcinol (BioDeep_00000174063)

   

human metabolite blood metabolite


代谢物信息卡片


5-(2-phenylethenyl)-1,3-benzenediol

化学式: C14H12O2 (212.0837252)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O
InChI: InChI=1S/C14H12O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-10,15-16H

描述信息

同义名列表

5 个代谢物同义名

5-(2-phenylethenyl)-1,3-benzenediol; 5-(2-phenylethenyl)benzene-1,3-diol; 5-(2-phenylvinyl)benzene-1,3-diol; 5-Styrylresorcinol; Pinosylvin



数据库引用编号

4 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)

49 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

  • Philippe Jeandet, Bertrand Delaunois, Aziz Aziz, David Donnez, Yann Vasserot, Sylvain Cordelier, Eric Courot. Metabolic engineering of yeast and plants for the production of the biologically active hydroxystilbene, resveratrol. Journal of biomedicine & biotechnology. 2012; 2012(?):579089. doi: 10.1155/2012/579089. [PMID: 22654481]
  • A Ludwiczuk, A Saha, T Kuzuhara, Y Asakawa. Bioactivity guided isolation of anticancer constituents from leaves of Alnus sieboldiana (Betulaceae). Phytomedicine : international journal of phytotherapy and phytopharmacology. 2011 Apr; 18(6):491-8. doi: 10.1016/j.phymed.2010.10.005. [PMID: 21111588]
  • Katarína Bauerová, Silvester Poništ, Danica Mihalová, František Dráfi, Viera Kuncírová. Utilization of adjuvant arthritis model for evaluation of new approaches in rheumatoid arthritis therapy focused on regulation of immune processes and oxidative stress. Interdisciplinary toxicology. 2011 Mar; 4(1):33-9. doi: 10.2478/v10102-011-0007-9. [PMID: 21577282]
  • Pilar Rodríguez-Bonilla, José Manuel López-Nicolás, Francisco García-Carmona. Use of reversed phase high pressure liquid chromatography for the physicochemical and thermodynamic characterization of oxyresveratrol/beta-cyclodextrin complexes. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2010 Jun; 878(19):1569-75. doi: 10.1016/j.jchromb.2010.04.016. [PMID: 20444655]
  • Supriya Baikar, Nutan Malpathak. Secondary metabolites as DNA topoisomerase inhibitors: A new era towards designing of anticancer drugs. Pharmacognosy reviews. 2010 Jan; 4(7):12-26. doi: 10.4103/0973-7847.65320. [PMID: 22228937]
  • Sung Ryeol Park, Jin A Yoon, Ji Hye Paik, Je Won Park, Won Seok Jung, Yeon-Hee Ban, Eun Ji Kim, Young Ji Yoo, Ah Reum Han, Yeo Joon Yoon. Engineering of plant-specific phenylpropanoids biosynthesis in Streptomyces venezuelae. Journal of biotechnology. 2009 May; 141(3-4):181-8. doi: 10.1016/j.jbiotec.2009.03.013. [PMID: 19433224]
  • Anni M Harju, Martti Venäläinen, Tapio Laakso, Pekka Saranpää. Wounding response in xylem of Scots pine seedlings shows wide genetic variation and connection with the constitutive defence of heartwood. Tree physiology. 2009 Jan; 29(1):19-25. doi: 10.1093/treephys/tpn006. [PMID: 19203929]
  • Kati Hanhineva, Harri Kokko, Henri Siljanen, Ilana Rogachev, Asaph Aharoni, Sirpa O Kärenlampi. Stilbene synthase gene transfer caused alterations in the phenylpropanoid metabolism of transgenic strawberry (Fragaria x ananassa). Journal of experimental botany. 2009; 60(7):2093-106. doi: 10.1093/jxb/erp085. [PMID: 19443619]
  • François Simard, Jean Legault, Serge Lavoie, Vakhtang Mshvildadze, André Pichette. Isolation and identification of cytotoxic compounds from the wood of Pinus resinosa. Phytotherapy research : PTR. 2008 Jul; 22(7):919-22. doi: 10.1002/ptr.2416. [PMID: 18389469]
  • Dong Zhang, Lan Yang, Mei-hong Fu, You-you Tu. [Studies on chemical constituents of rhizome of Matteuccia struthiopteris]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2008 Jul; 33(14):1703-5. doi: ". [PMID: 18841771]
  • Connie M Remsberg, Jaime A Yáñez, Kathryn A Roupe, Neal M Davies. High-performance liquid chromatographic analysis of pterostilbene in biological fluids using fluorescence detection. Journal of pharmaceutical and biomedical analysis. 2007 Jan; 43(1):250-4. doi: 10.1016/j.jpba.2006.06.035. [PMID: 16884886]
  • Kathryn A Roupe, Jaime A Yáñez, Xiao Wei Teng, Neal M Davies. Pharmacokinetics of selected stilbenes: rhapontigenin, piceatannol and pinosylvin in rats. The Journal of pharmacy and pharmacology. 2006 Nov; 58(11):1443-50. doi: 10.1211/jpp.58.11.0004. [PMID: 17132206]
  • Jin-Chun Cheng, Jian-Guo Fang, Wei-Feng Chen, Bo Zhou, Li Yang, Zhong-Li Liu. Structure-activity relationship studies of resveratrol and its analogues by the reaction kinetics of low density lipoprotein peroxidation. Bioorganic chemistry. 2006 Jun; 34(3):142-57. doi: 10.1016/j.bioorg.2006.04.001. [PMID: 16712899]
  • Dag Ekeberg, Per-Otto Flaete, Morten Eikenes, Monica Fongen, Carl Fredrik Naess-Andresen. Qualitative and quantitative determination of extractives in heartwood of Scots pine (Pinus sylvestris L.) by gas chromatography. Journal of chromatography. A. 2006 Mar; 1109(2):267-72. doi: 10.1016/j.chroma.2006.01.027. [PMID: 16472534]
  • Hanne Hovelstad, Ingebjorg Leirset, Karin Oyaas, Anne Fiksdahl. Screening analyses of pinosylvin stilbenes, resin acids and lignans in Norwegian conifers. Molecules (Basel, Switzerland). 2006 Jan; 11(1):103-14. doi: 10.3390/11010103. [PMID: 17962750]
  • Kathryn A Roupe, Connie M Remsberg, Jaime A Yáñez, Neal M Davies. Pharmacometrics of stilbenes: seguing towards the clinic. Current clinical pharmacology. 2006 Jan; 1(1):81-101. doi: 10.2174/157488406775268246. [PMID: 18666380]
  • Liliya Serazetdinova, Klaus H Oldach, Horst Lörz. Expression of transgenic stilbene synthases in wheat causes the accumulation of unknown stilbene derivatives with antifungal activity. Journal of plant physiology. 2005 Sep; 162(9):985-1002. doi: 10.1016/j.jplph.2004.11.005. [PMID: 16173460]
  • Gao Li, Byung-Sun Min, Changji Zheng, Joongku Lee, Sei-Ryang Oh, Kyung-Seop Ahn, Hyeong-Kyu Lee. Neuroprotective and free radical scavenging activities of phenolic compounds from Hovenia dulcis. Archives of pharmacal research. 2005 Jul; 28(7):804-9. doi: 10.1007/bf02977346. [PMID: 16114495]
  • Kathryn Roupe, Steven Halls, Neal M Davies. Determination and assay validation of pinosylvin in rat serum: application to drug metabolism and pharmacokinetics. Journal of pharmaceutical and biomedical analysis. 2005 Jun; 38(1):148-54. doi: 10.1016/j.jpba.2004.12.015. [PMID: 15907633]
  • S K Lee, H J Lee, H Y Min, E J Park, K M Lee, Y H Ahn, Y J Cho, J H Pyee. Antibacterial and antifungal activity of pinosylvin, a constituent of pine. Fitoterapia. 2005 Mar; 76(2):258-60. doi: 10.1016/j.fitote.2004.12.004. [PMID: 15752644]
  • M Nuopponen, S Willför, A-S Jääskeläinen, T Vuorinen. A UV resonance Raman (UVRR) spectroscopic study on the extractable compounds in Scots pine (Pinus sylvestris) wood. Part II. Hydrophilic compounds. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2004 Nov; 60(13):2963-8. doi: 10.1016/j.saa.2004.02.007. [PMID: 15477131]
  • S-K Seppänen, L Syrjälä, K von Weissenberg, T H Teeri, L Paajanen, A Pappinen. Antifungal activity of stilbenes in in vitro bioassays and in transgenic Populus expressing a gene encoding pinosylvin synthase. Plant cell reports. 2004 Mar; 22(8):584-93. doi: 10.1007/s00299-003-0728-0. [PMID: 14714142]
  • L E Lindberg, S M Willför, B R Holmbom. Antibacterial effects of knotwood extractives on paper mill bacteria. Journal of industrial microbiology & biotechnology. 2004 Mar; 31(3):137-47. doi: 10.1007/s10295-004-0132-y. [PMID: 15112061]
  • William R McNee, Pierluigi Bonello, Andrew J Storer, David L Wood, Thomas R Gordon. Feeding response of Ips paraconfusus to phloem and phloem metabolites of Heterobasidion annosum-inoculated ponderosa pine, Pinus ponderosa. Journal of chemical ecology. 2003 May; 29(5):1183-202. doi: 10.1023/a:1023885724220. [PMID: 12857030]
  • Eckhard Wollenweber, Jan F Stevens, Marion Dörr, Andrew C Rozefelds. Taxonomic significance of flavonoid variation in temperate species of Nothofagus. Phytochemistry. 2003 Apr; 62(7):1125-31. doi: 10.1016/s0031-9422(02)00666-0. [PMID: 12591267]
  • Yu Jun Cai, Jian Guo Fang, Lan Ping Ma, Li Yang, Zhong Li Liu. Inhibition of free radical-induced peroxidation of rat liver microsomes by resveratrol and its analogues. Biochimica et biophysica acta. 2003 Jan; 1637(1):31-8. doi: 10.1016/s0925-4439(02)00174-6. [PMID: 12527404]
  • Jian-Guo Fang, Man Lu, Zhi-Hua Chen, Hui-He Zhu, Yan Li, Li Yang, Long-Min Wu, Zhong-Li Liu. Antioxidant effects of resveratrol and its analogues against the free-radical-induced peroxidation of linoleic acid in micelles. Chemistry (Weinheim an der Bergstrasse, Germany). 2002 Sep; 8(18):4191-8. doi: 10.1002/1521-3765(20020916)8:18<4191::aid-chem4191>3.0.co;2-s. [PMID: 12298009]
  • T Pacher, C Seger, D Engelmeier, S Vajrodaya, O Hofer, H Greger. Antifungal stilbenoids from Stemona collinsae. Journal of natural products. 2002 Jun; 65(6):820-7. doi: 10.1021/np0105073. [PMID: 12088422]
  • Mikael Nilsson, Susanne Wikman, Leif Eklund. Induction of discolored wood in Scots pine (Pinus sylvestris). Tree physiology. 2002 Apr; 22(5):331-8. doi: 10.1093/treephys/22.5.331. [PMID: 11960757]
  • Christelle Privat, João Paulo Telo, Vania Bernardes-Genisson, Abel Vieira, Jean-Pierre Souchard, Françoise Nepveu. Antioxidant properties of trans-epsilon-viniferin as compared to stilbene derivatives in aqueous and nonaqueous media. Journal of agricultural and food chemistry. 2002 Feb; 50(5):1213-7. doi: 10.1021/jf010676t. [PMID: 11853506]
  • S Stojanović, H Sprinz, O Brede. Efficiency and mechanism of the antioxidant action of trans-resveratrol and its analogues in the radical liposome oxidation. Archives of biochemistry and biophysics. 2001 Jul; 391(1):79-89. doi: 10.1006/abbi.2001.2388. [PMID: 11414688]