Farnesyl acetate (BioDeep_00000019378)

 

Secondary id: BioDeep_00000228120, BioDeep_00000395639, BioDeep_00000418807

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


Acetic acid (2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl ester

化学式: C17H28O2 (264.2089188)
中文名称: 金合欢醇乙酸酯 (异构体混合物), 反式,反式-十八烷基乙酸酯, 3,7,11-三甲基-2,6,10-十二烷三烯-1-醇乙酸酯, 醋酸法尼基酯
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 9.41%

分子结构信息

SMILES: C(=C\CC/C(=C/COC(=O)C)/C)(\C)/CCC=C(C)C
InChI: InChI=1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3

描述信息

Farnesyl acetate (CAS: 29548-30-9) is a flavouring compound. Farnesyl acetate has been identified in foods such as blueberries.
Flavouring compound [Flavornet]

同义名列表

22 个代谢物同义名

Acetic acid (2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl ester; (2E,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-yl acetate; 1-Acetoxy-3,7,11-trimethyl-2,6,10-dodecatriene; 3,7,11-Trimethyldodeca-2,6,10-trienyl acetate; 3,7,11-Trimethyl-2,6,10-dodecatrienyl acetate; 2-trans-6-trans-Farnesyl acetic acid; Acetic acid (2E,6E)-farnesyl ester; Farnesylacetic acid, (e,e)-isomer; 2-trans-6-trans-Farnesyl acetate; trans-2-trans-6-Farnesyl acetate; trans,trans-Farnesyl acetate; trans,trans-Farnesol acetate; all-trans-Farnesyl acetate; Acetic acid farnesyl ester; (2E,6E)-Farnesyl acetate; (E,E)-Farnesyl acetate; Farnesyl acetic acid; Farnesylacetic acid; Farnesyl acetate; Farnesol acetate; Farnesylacetate; Farnesyl acetate



数据库引用编号

14 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)

57 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

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  • Miklós Tóth, Lorenzo Furlan, István Szarukán, Antal Nagy, József Vuts, Teodora Toshova, Dimitar Velchev, Zsófia Lohonyai, Zoltán Imrei. The Addition of a Pheromone to a Floral Lure Increases Catches of Females of the Click Beetle Agriotes ustulatus (Schaller) (Coleoptera: Elateridae). Journal of chemical ecology. 2019 Aug; 45(8):667-672. doi: 10.1007/s10886-019-01087-z. [PMID: 31313134]
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  • Khalijah Awang, Halijah Ibrahim, Devi Rosmy Syamsir, Mastura Mohtar, Rasadah Mat Ali, Nor Azah Mohamad Ali. Chemical constituents and antimicrobial activity of the leaf and rhizome oils of Alpinia pahangensis Ridl., an endemic wild ginger from peninsular Malaysia. Chemistry & biodiversity. 2011 Apr; 8(4):668-73. doi: 10.1002/cbdv.201000225. [PMID: 21480512]
  • Wan Mohd Nuzul Hakimi Wan Salleh, Farediah Ahmad, Khong Heng Yen, Hasnah Mohd Sirat. Chemical compositions, antioxidant and antimicrobial activities of essential oils of Piper caninum Blume. International journal of molecular sciences. 2011; 12(11):7720-31. doi: 10.3390/ijms12117720. [PMID: 22174627]
  • T K Praveen, S Dharmaraj, Jitendra Bajaj, S P Dhanabal, S Manimaran, M J Nanjan, Rema Razdan. Hepatoprotective activity of petroleum ether, diethyl ether, and methanol extract of Scoparia dulcis L. against CCl4-induced acute liver injury in mice. Indian journal of pharmacology. 2009 Jun; 41(3):110-4. doi: 10.4103/0253-7613.55206. [PMID: 20442817]
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  • Miklós Tóth, Lorenzo Furlan, Amália Xavier, József Vuts, Teodora Toshova, Mitko Subchev, István Szarukán, Venyamin Yatsynin. New sex attractant composition for the click beetle Agriotes proximus: similarity to the pheromone of Agriotes lineatus. Journal of chemical ecology. 2008 Jan; 34(1):107-11. doi: 10.1007/s10886-007-9398-7. [PMID: 18064523]
  • Anders Vik, Anthony James, Lise-Lotte Gundersen. Screening of terpenes and derivatives for antimycobacterial activity; identification of geranylgeraniol and geranylgeranyl acetate as potent inhibitors of Mycobacterium tuberculosis in vitro. Planta medica. 2007 Oct; 73(13):1410-2. doi: 10.1055/s-2007-990238. [PMID: 17924309]
  • Kurt Mendgen, Stefan G R Wirsel, Andreas Jux, Jochen Hoffmann, Wilhelm Boland. Volatiles modulate the development of plant pathogenic rust fungi. Planta. 2006 Nov; 224(6):1353-61. doi: 10.1007/s00425-006-0320-2. [PMID: 16775700]
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  • Miklós Tóth, Lorenzo Furlan, Venyamin G Yatsynin, István Ujváry, István Szarukán, Zoltán Imrei, Till Tolasch, Wittko Francke, Werner Jossi. Identification of pheromones and optimization of bait composition for click beetle pests (Coleoptera: Elateridae) in Central and Western Europe. Pest management science. 2003 Apr; 59(4):417-25. doi: 10.1002/ps.629. [PMID: 12701702]
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