alpha-Farnesene (BioDeep_00000000722)

Main id: BioDeep_00000859692

Secondary id: BioDeep_00001891810

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


3,7,11-Trimethyl-1,3,6,10-dodecatetraene, (trans,trans)-

化学式: C15H24 (204.18779039999998)
中文名称: 金合欢烯,异构体混合物, α-法呢烯, α-法呢烯
谱图信息: 最多检出来源 Homo sapiens(feces) 0.48%

分子结构信息

SMILES: C=C/C(=C/C/C=C(\C)/CCC=C(C)C)/C
InChI: InChI=1S/C15H24/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9-10,12H,1,7-8,11H2,2-5H3/b14-10+,15-12+

描述信息

alpha-Farnesene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (3E,6E)-alpha-Farnesene, also known as trans-alpha-Farnesene, is a sweet, bergamot, and citrus tasting flavouring ingredient. (3E,6E)-alpha-Farnesene is a constituent of the natural coating of apples and pears and other fruit. It has been identified in gingers, cottonseeds, common oregano, sweet oranges, spearmints, guava, pomes, and pears. This could make (3E,6E)-alpha-farnesene a potential biomarker for the consumption of these foods.
Alpha-farnesene is a farnesene that is 1,3,6,10-tetraene substituted by methyl groups at positions 3, 7 and 11 respectively.
alpha-Farnesene is a natural product found in Eupatorium cannabinum, Lonicera japonica, and other organisms with data available.
See also: Chamomile (part of); Cannabis sativa subsp. indica top (part of).
Constituent of the natural coating of apples and pears and other fruit. Flavouring ingredient. (3E,6E)-alpha-Farnesene is found in many foods, some of which are cottonseed, spearmint, ginger, and fruits.

同义名列表

60 个代谢物同义名

3,7,11-Trimethyl-1,3,6,10-dodecatetraene, (trans,trans)-; 1,3,6,10-Dodecatetraene, 3,7,11-trimethyl-, (3E,6E)-; 1,3,6,10-Dodecatetraene, 3,7,11-trimethyl-, (E,E)-; (3E,6E)-3,7,11-Trimethyl-1,3,6,10-dodecatetraene #; (3E,6E)-3,7,11-trimethyl-dodeca-1,3,6,10-tetraene; (3E,6E)-3,7,11-trimethyldodeca-1,3,6,10-tetraene; (3E,6E)-3,7,11-Trimethyl-1,3,6,10-dodecatetraene; 2,6,10-Trimethyl-2,6,9,11-dodecatetraene, trans-; trans-2,6,10-Trimethyl-2,6,9,11-dodecatetraene; 3,7,11-Trimethyl-(E,E)-1,3,6,10-dodecatetraene; trans-3,7,11-Trimethyl-1,3,6,10-dodecatetraene; 1,3,6,10-Dodecatetraene, 3,7,11-trimethyl-; 3,7,11-Trimethyl-dodeca-1,3,6,10-tetraene; 3,7,11-Trimethyl-1,3,6,10-dodecatetraene; 2,6,10-Trimethyldodeca-2,6,9,11-tetraene; 3,7,11-trimethyldodeca-1,3,6,10-tetraene; trans,trans-.alpha.-Farnesene; .alpha.-trans,trans-Farnesene; .alpha.-Farnesene (isomer 1); alpha-trans,trans-Farnesene; trans,trans-alpha-farnesene; CXENHBSYCFFKJS-GZCJILEISA-N; (3E,6E)- .alpha.-Farnesene; (3E,6E)-.ALPHA.-FARNESENE; alpha-Farnesene (natural); .alpha.-Farnesene, (E,E)-; .alpha.-Farnesene isomer; (E,E)-.alpha.-Farnesene; trans-.alpha.-Farnesene; trans,trans-α-Farnesene; (3E,6E)-alpha-Farnesene; .alpha.-trans-Farnesene; .ALPHA.-FARNESENE [MI]; farnesene (e,e-alpha-); (E,E)-alpha-farnesene; .alpha.-E,E-Farnesene; trans-alpha-farnesene; (E)-alpha-Farnesene; (3E,6E)-Α-farnesene; (3E,6E)-a-Farnesene; Sesquicitronellene; .alpha.-Farnesene; (E,E)-α-Farnesene; trans-α-Farnesene; alpha.-Farnesene; UNII-7E1785CZ0H; Alpha-Farnesene; trans-Farnesene; (E,E)-Farnesene; (E/Z)-Farnesene; I+/--farnesene; ??-Farnesene; Tox21_303626; α-Farnesene; a-farnesene; 7E1785CZ0H; FARNESENE-; Farnesene; (E,E)- -farnesene; α-Farnesene



数据库引用编号

24 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(0)

代谢反应

3 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(2)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

114 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

  • Wu Wang, Mindy Wang, Jiao Feng, Shijie Zhang, Yu Chen, Yuqiang Zhao, Ruiping Tian, Cancan Zhu, Niels J Nieuwenhuizen. Terpene Synthase Gene Family in Chinese Chestnut (Castanea mollissima BL.) Harbors Two Sesquiterpene Synthase Genes Implicated in Defense against Gall Wasp Dryocosmus kuriphilus. Journal of agricultural and food chemistry. 2024 Jan; 72(3):1571-1581. doi: 10.1021/acs.jafc.3c07086. [PMID: 38206573]
  • Dalila Touhami, Adedayo O Mofikoya, Robbie D Girling, Ben Langford, Pawel K Misztal, Christian Pfrang. Atmospheric Degradation of Ecologically Important Biogenic Volatiles: Investigating the Ozonolysis of (E)-β-Ocimene, Isomers of α and β-Farnesene, α-Terpinene and 6-Methyl-5-Hepten-2-One, and Their Gas-Phase Products. Journal of chemical ecology. 2024 Jan; ?(?):. doi: 10.1007/s10886-023-01467-6. [PMID: 38195852]
  • Xiaoyue Lun, Xiuxiu Xu, Yu Zhang, Ruirui Zhang, Yan Cao, Xiangzhi Zhang, Meina Jin, Zhengqun Zhang, Yunhe Zhao. An Antennae-Enriched Odorant-Binding Protein EonuOBP43 Mediate the Behavioral Response of the Tea Green Leafhopper, Empoasca onukii Matsuda to the Host and Nonhost Volatiles. Journal of agricultural and food chemistry. 2023 Dec; 71(50):20000-20010. doi: 10.1021/acs.jafc.3c07144. [PMID: 38059819]
  • Jossiê Zamperetti Donadel, Fabio Rodrigo Thewes, Luana Ferreira Dos Santos, Erani Eliseu Schultz, Magno Roberto Pasquetti Berghetti, Vagner Ludwig, Juliana Mesadri, Bruna Klein, Flavio Roberto Thewes, Suele Fernanda Prediger Schmidt, Vanderlei Both, Auri Brackmann, Daniel Alexandre Neuwald, Roger Wagner. Superficial scald development in 'Granny Smith' and 'Nicoter' apples: The role of key volatile compounds when fruit are stored under dynamic controlled atmosphere. Food research international (Ottawa, Ont.). 2023 Nov; 173(Pt 2):113396. doi: 10.1016/j.foodres.2023.113396. [PMID: 37803734]
  • Xinhua Zhang, Xiaohong Chen, Jaime A Teixeira da Silva, Ting Zhang, Yuping Xiong, Yuan Li, Yunfei Yuan, Xiaoping Pan, Guohua Ma. Characterization of sandalwood (E,E)-α-farnesene synthase whose overexpression enhances cold tolerance through jasmonic acid biosynthesis and signaling in Arabidopsis. Planta. 2023 Jul; 258(3):54. doi: 10.1007/s00425-023-04212-1. [PMID: 37515637]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Liliane Sena Pinheiro, Valter Viana Andrade-Neto, Marcio Mantuano-Barradas, Elisa Cavalcante Pereira, Rodrigo Cesar Fernandes Barbosa, Marcia Cristina Campos de Oliveira, Rubem Figueiredo Sadok Menna-Barreto, Edézio Ferreira Cunha-Júnior, Eduardo Caio Torres-Santos. Biological effects of trans, trans-farnesol in Leishmania amazonensis. Frontiers in cellular and infection microbiology. 2023; 13(?):1221246. doi: 10.3389/fcimb.2023.1221246. [PMID: 38035328]
  • Shuhua Wu, Yuhua Yang, Jiaming Chen, Jianlong Li, Guotai Jian, Jie Yang, Kaiquan Mao, Lanting Zeng, Dachuan Gu. Histone deacetylase CsHDA6 mediates the regulated formation of the anti-insect metabolite α-farnesene in tea (Camellia sinensis). Plant science : an international journal of experimental plant biology. 2023 Jan; 326(?):111501. doi: 10.1016/j.plantsci.2022.111501. [PMID: 36257410]
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  • Leo Lebanov, Shing Chung Lam, Laura Tedone, Tomislav Sostaric, Jason A Smith, Alireza Ghiasvand, Brett Paull. Radical scavenging activity and metabolomic profiling study of ylang-ylang essential oils based on high-performance thin-layer chromatography and multivariate statistical analysis. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2021 Aug; 1179(?):122861. doi: 10.1016/j.jchromb.2021.122861. [PMID: 34339956]
  • Christelle Lemaitre-Guillier, Christelle Dufresne, Agnès Chartier, Stéphanie Cluzet, Josep Valls, Lucile Jacquens, Antonin Douillet, Nicolas Aveline, Marielle Adrian, Xavier Daire. VOCs Are Relevant Biomarkers of Elicitor-Induced Defences in Grapevine. Molecules (Basel, Switzerland). 2021 Jul; 26(14):. doi: 10.3390/molecules26144258. [PMID: 34299533]
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  • Jieyang Jin, Shangrui Zhang, Mingyue Zhao, Tingting Jing, Na Zhang, Jingming Wang, Bin Wu, Chuankui Song. Scenarios of Genes-to-Terpenoids Network Led to the Identification of a Novel α/β-Farnesene/β-Ocimene Synthase in Camellia sinensis. International journal of molecular sciences. 2020 Jan; 21(2):. doi: 10.3390/ijms21020655. [PMID: 31963919]
  • Edwige J F Souleyre, Joanna K Bowen, Adam J Matich, Sumathi Tomes, Xiuyin Chen, Martin B Hunt, Mindy Y Wang, Nadeesha R Ileperuma, Kate Richards, Daryl D Rowan, David Chagné, Ross G Atkinson. Genetic control of α-farnesene production in apple fruit and its role in fungal pathogenesis. The Plant journal : for cell and molecular biology. 2019 12; 100(6):1148-1162. doi: 10.1111/tpj.14504. [PMID: 31436867]
  • Xuewen Wang, Lanting Zeng, Yinyin Liao, Jianlong Li, Jinchi Tang, Ziyin Yang. Formation of α-Farnesene in Tea (Camellia sinensis) Leaves Induced by Herbivore-Derived Wounding and Its Effect on Neighboring Tea Plants. International journal of molecular sciences. 2019 Aug; 20(17):. doi: 10.3390/ijms20174151. [PMID: 31450700]
  • Chia-Ming Liu, Shigeru Matsuyama, Yooichi Kainoh. Synergistic Effects of Volatiles from Host-Infested Plants on Host-Searching Behavior in the Parasitoid Wasp Lytopylus rufipes (Hymenoptera: Braconidae). Journal of chemical ecology. 2019 Aug; 45(8):684-692. doi: 10.1007/s10886-019-01088-y. [PMID: 31289990]
  • Bastien Durenne, Alodie Blondel, Philippe Druart, Marie-Laure Fauconnier. Epoxiconazole exposure affects terpenoid profiles of oilseed rape plantlets based on a targeted metabolomic approach. Environmental science and pollution research international. 2019 Jun; 26(17):17362-17372. doi: 10.1007/s11356-019-05110-4. [PMID: 31012076]
  • Wirginia Kukula-Koch, Wojciech Koch, Lidia Czernicka, Kazimierz Głowniak, Yoshinori Asakawa, Akemi Umeyama, Zbigniew Marzec, Takashi Kuzuhara. MAO-A Inhibitory Potential of Terpene Constituents from Ginger Rhizomes-A Bioactivity Guided Fractionation. Molecules (Basel, Switzerland). 2018 May; 23(6):. doi: 10.3390/molecules23061301. [PMID: 29844252]
  • Nitirat Chimnoi, Nanthawan Reuk-Ngam, Piyachat Chuysinuan, Panita Khlaychan, Nisachon Khunnawutmanotham, Daranee Chokchaichamnankit, Wassapol Thamniyom, Srikanjana Klayraung, Chulabhorn Mahidol, Supanna Techasakul. Characterization of essential oil from Ocimum gratissimum leaves: Antibacterial and mode of action against selected gastroenteritis pathogens. Microbial pathogenesis. 2018 May; 118(?):290-300. doi: 10.1016/j.micpath.2018.03.041. [PMID: 29578062]
  • Lanting Zeng, Yinyin Liao, Jianlong Li, Ying Zhou, Jinchi Tang, Fang Dong, Ziyin Yang. α-Farnesene and ocimene induce metabolite changes by volatile signaling in neighboring tea (Camellia sinensis) plants. Plant science : an international journal of experimental plant biology. 2017 Nov; 264(?):29-36. doi: 10.1016/j.plantsci.2017.08.005. [PMID: 28969800]
  • Ying Yu, Shiheng Lyu, Dan Chen, Yi Lin, Jianjun Chen, Guixin Chen, Naixing Ye. Volatiles Emitted at Different Flowering Stages of Jasminum sambac and Expression of Genes Related to α-Farnesene Biosynthesis. Molecules (Basel, Switzerland). 2017 Mar; 22(4):. doi: 10.3390/molecules22040546. [PMID: 28353656]
  • Yu Liu, Lu Wang, Heng Liu, Rongrong Zhao, Bin Liu, Quanjuan Fu, Yuanhu Zhang. The antioxidative defense system is involved in the premature senescence in transgenic tobacco (Nicotiana tabacum NC89). Biological research. 2016 Jul; 49(1):30. doi: 10.1186/s40659-016-0088-1. [PMID: 27370650]
  • Tomonori Asai, Tetsuya Matsukawa, Shin'ichiro Kajiyama. Metabolic changes in Citrus leaf volatiles in response to environmental stress. Journal of bioscience and bioengineering. 2016 Feb; 121(2):235-41. doi: 10.1016/j.jbiosc.2015.06.004. [PMID: 26188419]
  • Rajesh K Joshi. E,E-α-Farnesene rich essential oil of Saraca asoca (Roxb.) Wilde flower. Natural product research. 2016; 30(8):979-81. doi: 10.1080/14786419.2015.1076818. [PMID: 26306003]
  • Kevin W George, Jorge Alonso-Gutierrez, Jay D Keasling, Taek Soon Lee. Isoprenoid drugs, biofuels, and chemicals--artemisinin, farnesene, and beyond. Advances in biochemical engineering/biotechnology. 2015; 148(?):355-89. doi: 10.1007/10_2014_288. [PMID: 25577395]
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  • Nicola Busatto, Brian Farneti, Alice Tadiello, Urska Vrhovsek, Luca Cappellin, Franco Biasioli, Riccardo Velasco, Guglielmo Costa, Fabrizio Costa. Target metabolite and gene transcription profiling during the development of superficial scald in apple (Malus x domestica Borkh). BMC plant biology. 2014 Jul; 14(?):193. doi: 10.1186/s12870-014-0193-7. [PMID: 25038781]
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  • Mayuree Kanlayavattanakul, Sarun Kitsiripaisarn, Nattaya Lourith. Aroma profiles and preferences of Jasminum sambac L. flowers grown in Thailand. Journal of cosmetic science. 2013 Nov; 64(6):483-93. doi: ". [PMID: 24397885]
  • Sergio López, Carmen Quero, Juan Carlos Iturrondobeitia, Angel Guerrero, Arturo Goldarazena. Electrophysiological and behavioural responses of Pityophthorus pubescens (Coleoptera: Scolytinae) to (E,E)-α-farnesene, (R)-(+)-limonene and (S)-(-)-verbenone in Pinus radiata (Pinaceae) stands in northern Spain. Pest management science. 2013 Jan; 69(1):40-7. doi: 10.1002/ps.3359. [PMID: 22764125]
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