(3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene (BioDeep_00000013614)

 

Secondary id: BioDeep_00000619086, BioDeep_00001868858, BioDeep_00001891441

human metabolite PANOMIX_OTCML-2023 Endogenous Volatile Flavor Compounds


代谢物信息卡片


(3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene

化学式: C16H26 (218.2034396)
中文名称: （3E，7E）-4,8,12-三甲基十三烷-1,3,7,11-四烯
谱图信息: 最多检出来源 Viridiplantae(plant) 0.06%

分子结构信息

SMILES: C(=CCC/C(=C/CC/C(=C/C=C)/C)/C)(C)C
InChI: InChI=1S/C16H26/c1-6-9-15(4)12-8-13-16(5)11-7-10-14(2)3/h6,9-10,13H,1,7-8,11-12H2,2-5H3/b15-9+,16-13+

描述信息

(3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene is found in cardamom. (3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene is a constituent of essential oil of Elettaria cardamomum (cardamom)
Constituent of essential oil of Elettaria cardamomum (cardamom). (3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene is found in cardamom, herbs and spices, and garden tomato (variety).

同义名列表

10 个代谢物同义名

(3E,7E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene; (3E,7E)-4,8,12-Trimethyltrideca 1,3,7,11-tetraene; (3E,7E)-4,8,12-Trimethyltrideca-1,3,7,11-tetraene; (E,E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene; (e,e)-4,8,12-Trimethyltrideca-1,3,7,11-tetraene; 4,8,12-Trimethyl-1,3E,7E,11-tridecatetraene; 4,8,12-Trimethyltrideca-1,3,7,11-tetraene; 4,8,12-trimethyl-1,3,7,11-tridecatetraene; TMTT; (3E,7E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene



数据库引用编号

12 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

62 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(2)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(60)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

3 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

  • Andja Vucetic, Iris Dahlin, Olivera Petrovic-Obradovic, Robert Glinwood, Ben Webster, Velemir Ninkovic. Volatile interaction between undamaged plants affects tritrophic interactions through changed plant volatile emission. Plant signaling & behavior. 2014; 9(8):e29517. doi: 10.4161/psb.29517. [PMID: 25763628]
  • Mahabaleshwar Hegde, Janser N Oliveira, Joao G da Costa, Elisa Loza-Reyes, Ervino Bleicher, Antonio E G Santana, John C Caulfield, Patrick Mayon, Sarah Y Dewhirst, Toby J A Bruce, John A Pickett, Michael A Birkett. Aphid antixenosis in cotton is activated by the natural plant defence elicitor cis-jasmone. Phytochemistry. 2012 Jun; 78(?):81-8. doi: 10.1016/j.phytochem.2012.03.004. [PMID: 22516741]
  • Sufang Zhang, Jianing Wei, Le Kang. Transcriptional analysis of Arabidopsis thaliana response to lima bean volatiles. PloS one. 2012; 7(4):e35867. doi: 10.1371/journal.pone.0035867. [PMID: 22558246]
  • Jurgen Engelberth, Claudia Fabiola Contreras, Sriram Viswanathan. Transcriptional analysis of distant signaling induced by insect elicitors and mechanical wounding in Zea mays. PloS one. 2012; 7(4):e34855. doi: 10.1371/journal.pone.0034855. [PMID: 22511969]
  • Martin Pareja, Erika Qvarfordt, Ben Webster, Patrick Mayon, John Pickett, Michael Birkett, Robert Glinwood. Herbivory by a Phloem-feeding insect inhibits floral volatile production. PloS one. 2012; 7(2):e31971. doi: 10.1371/journal.pone.0031971. [PMID: 22384116]
  • Dorothea Tholl, Reza Sohrabi, Jung-Hyun Huh, Sungbeom Lee. The biochemistry of homoterpenes--common constituents of floral and herbivore-induced plant volatile bouquets. Phytochemistry. 2011 Sep; 72(13):1635-46. doi: 10.1016/j.phytochem.2011.01.019. [PMID: 21334702]
  • J Daniel Hare, Jia J Sun. Production of induced volatiles by Datura wrightii in response to damage by insects: effect of herbivore species and time. Journal of chemical ecology. 2011 Jul; 37(7):751-64. doi: 10.1007/s10886-011-9985-5. [PMID: 21691808]
  • Juliana Almeida, Leandro Quadrana, Ramón Asís, Nathalia Setta, Fabiana de Godoy, Luisa Bermúdez, Santiago N Otaiza, Junia V Corrêa da Silva, Alisdair R Fernie, Fernando Carrari, Magdalena Rossi. Genetic dissection of vitamin E biosynthesis in tomato. Journal of experimental botany. 2011 Jul; 62(11):3781-98. doi: 10.1093/jxb/err055. [PMID: 21527625]
  • Renato Almeida Sarmento, Felipe Lemos, Petra M Bleeker, Robert C Schuurink, Angelo Pallini, Maria Goreti Almeida Oliveira, Eraldo R Lima, Merijn Kant, Maurice W Sabelis, Arne Janssen. A herbivore that manipulates plant defence. Ecology letters. 2011 Mar; 14(3):229-36. doi: 10.1111/j.1461-0248.2010.01575.x. [PMID: 21299823]
  • Sunday Oluwafemi, Toby J A Bruce, John A Pickett, Jurriaan Ton, Michael A Birkett. Behavioral responses of the leafhopper, Cicadulina storeyi China, a major vector of maize streak virus, to volatile cues from intact and leafhopper-damaged maize. Journal of chemical ecology. 2011 Jan; 37(1):40-8. doi: 10.1007/s10886-010-9891-2. [PMID: 21191806]
  • Michiel van Wijk, Paulien J A de Bruijn, Maurice W Sabelis. Complex odor from plants under attack: herbivore's enemies react to the whole, not its parts. PloS one. 2011; 6(7):e21742. doi: 10.1371/journal.pone.0021742. [PMID: 21765908]
  • Tjeerd A L Snoeren, Iris F Kappers, Colette Broekgaarden, Roland Mumm, Marcel Dicke, Harro J Bouwmeester. Natural variation in herbivore-induced volatiles in Arabidopsis thaliana. Journal of experimental botany. 2010 Jun; 61(11):3041-56. doi: 10.1093/jxb/erq127. [PMID: 20488836]
  • Ben Webster, Salvador Gezan, Toby Bruce, Jim Hardie, John Pickett. Between plant and diurnal variation in quantities and ratios of volatile compounds emitted by Vicia faba plants. Phytochemistry. 2010 Jan; 71(1):81-9. doi: 10.1016/j.phytochem.2009.09.029. [PMID: 19863976]
  • Tjeerd A L Snoeren, Remco M P Van Poecke, Marcel Dicke. Multidisciplinary approach to unravelling the relative contribution of different oxylipins in indirect defense of Arabidopsis thaliana. Journal of chemical ecology. 2009 Sep; 35(9):1021-31. doi: 10.1007/s10886-009-9696-3. [PMID: 19798534]
  • Christian Abel, Maria Clauss, Andrea Schaub, Jonathan Gershenzon, Dorothea Tholl. Floral and insect-induced volatile formation in Arabidopsis lyrata ssp. petraea, a perennial, outcrossing relative of A. thaliana. Planta. 2009 Jun; 230(1):1-11. doi: 10.1007/s00425-009-0921-7. [PMID: 19322583]
  • Elham Attaran, Michael Rostás, Jürgen Zeier. Pseudomonas syringae elicits emission of the terpenoid (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene in Arabidopsis leaves via jasmonate signaling and expression of the terpene synthase TPS4. Molecular plant-microbe interactions : MPMI. 2008 Nov; 21(11):1482-97. doi: 10.1094/mpmi-21-11-1482. [PMID: 18842097]
  • Ben Webster, Toby Bruce, Samuel Dufour, Claudia Birkemeyer, Michael Birkett, Jim Hardie, John Pickett. Identification of volatile compounds used in host location by the black bean aphid, Aphis fabae. Journal of chemical ecology. 2008 Sep; 34(9):1153-61. doi: 10.1007/s10886-008-9510-7. [PMID: 18584254]
  • Marco Herde, Katrin Gärtner, Tobias G Köllner, Benjamin Fode, Wilhelm Boland, Jonathan Gershenzon, Christiane Gatz, Dorothea Tholl. Identification and regulation of TPS04/GES, an Arabidopsis geranyllinalool synthase catalyzing the first step in the formation of the insect-induced volatile C16-homoterpene TMTT. The Plant cell. 2008 Apr; 20(4):1152-68. doi: 10.1105/tpc.106.049478. [PMID: 18398052]
  • Gen-ichiro Arimura, Stefan Garms, Massimo Maffei, Simone Bossi, Birgit Schulze, Margit Leitner, Axel Mithöfer, Wilhelm Boland. Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling. Planta. 2008 Jan; 227(2):453-64. doi: 10.1007/s00425-007-0631-y. [PMID: 17924138]
  • Kai Ament, Chris C Van Schie, Harro J Bouwmeester, Michel A Haring, Robert C Schuurink. Induction of a leaf specific geranylgeranyl pyrophosphate synthase and emission of (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene in tomato are dependent on both jasmonic acid and salicylic acid signaling pathways. Planta. 2006 Oct; 224(5):1197-208. doi: 10.1007/s00425-006-0301-5. [PMID: 16786318]
  • Jia-Ning Wei, Le Kang. Electrophysiological and behavioral responses of a parasitic wasp to plant volatiles induced by two leaf miner species. Chemical senses. 2006 Jun; 31(5):467-77. doi: 10.1093/chemse/bjj051. [PMID: 16621971]
  • Jetske G de Boer, Maarten A Posthumus, Marcel Dicke. Identification of volatiles that are used in discrimination between plants infested with prey or nonprey herbivores by a predatory mite. Journal of chemical ecology. 2004 Nov; 30(11):2215-30. doi: 10.1023/b:joec.0000048784.79031.5e. [PMID: 15672666]
  • Terhi Vuorinen, Anne-Marja Nerg, Jarmo K Holopainen. Ozone exposure triggers the emission of herbivore-induced plant volatiles, but does not disturb tritrophic signalling. Environmental pollution (Barking, Essex : 1987). 2004 Sep; 131(2):305-11. doi: 10.1016/j.envpol.2004.02.027. [PMID: 15234097]
  • J L Blackmer, C Rodriguez-Saona, J A Byers, K L Shope, J P Smith. Behavioral response of Lygus hesperus to conspecifics and headspace volatiles of alfalfa in a Y-tube olfactometer. Journal of chemical ecology. 2004 Aug; 30(8):1547-64. doi: 10.1023/b:joec.0000042067.27698.30. [PMID: 15537158]
  • Stefano Colazza, J Steven McElfresh, Jocelyn G Millar. Identification of volatile synomones, induced by Nezara viridula feeding and oviposition on bean spp., that attract the egg parasitoid Trissolcus basalis. Journal of chemical ecology. 2004 May; 30(5):945-64. doi: 10.1023/b:joec.0000028460.70584.d1. [PMID: 15274441]
  • Cláudia A Zini, Kelen D Zanin, Eva Christensen, Elina B Caramão, Janusz Pawliszyn. Solid-phase microextraction of volatile compounds from the chopped leaves of three species of Eucalyptus. Journal of agricultural and food chemistry. 2003 Apr; 51(9):2679-86. doi: 10.1021/jf026047g. [PMID: 12696957]
  • C Rodriguez-Saona, S J Crafts-Brandner, P W Paré, T J Henneberry. Exogenous methyl jasmonate induces volatile emissions in cotton plants. Journal of chemical ecology. 2001 Apr; 27(4):679-95. doi: 10.1023/a:1010393700918. [PMID: 11446293]
  • J Engelberth, T Koch, G Schüler, N Bachmann, J Rechtenbach, W Boland. Ion channel-forming alamethicin is a potent elicitor of volatile biosynthesis and tendril coiling. Cross talk between jasmonate and salicylate signaling in lima bean. Plant physiology. 2001 Jan; 125(1):369-77. doi: 10.1104/pp.125.1.369. [PMID: 11154344]