Linalyl oxide (BioDeep_00000017666)

 

Secondary id: BioDeep_00000620099

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


2-Furanmethanol, 5-ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-, (2R,5S)-rel-

化学式: C10H18O2 (170.1307)
中文名称: 氧化芳樟醇, 氧化芳樟醇(异构体混合物)
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 19.74%

分子结构信息

SMILES: C1C[C@@H](O[C@]1(C=C)C)C(C)(O)C
InChI: InChI=1S/C10H18O2/c1-5-10(4)7-6-8(12-10)9(2,3)11/h5,8,11H,1,6-7H2,2-4H3

描述信息

Linalyl oxide is found in citrus. Linalyl oxide is isolated from Citrus paradisi (grapefruit), Thea sinensis (tea) and many other sources. Linalyl oxide is a flavouring ingredient.This is the furanoid form of linalool oxide; there are 4 possible stereo-isomers
Linalyl oxide is a member of oxolanes.
Linalyl oxide is a natural product found in Pulicaria arabica, Carica papaya, and Camellia sinensis with data available.
Isolated from Citrus paradisi (grapefruit), Thea sinensis (tea) and many other sources. Flavouring ingredient
Linalool oxide is a secondary metabolite in elongating wheat plants with antinociceptive and anticonvulsant effects. Linalool oxide shows anxiolytic activity[1][2][3].
Linalool oxide is a secondary metabolite in elongating wheat plants with antinociceptive and anticonvulsant effects. Linalool oxide shows anxiolytic activity[1][2][3].

同义名列表

71 个代谢物同义名

2-Furanmethanol, 5-ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-, (2R,5S)-rel-; 2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, (2R,5R)-rel-; 2-Furanmethanol, 5-ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-, trans-; 2-Furanmethanol, 5-ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-, cis-; Furfuryl alcohol, tetrahydro-.alpha.,.alpha.,5-trimethyl-5-vinyl-, cis-; trans-5-Ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-2-furanmethanol; cis-5-Ethenyltetrahydro-.alpha.,.alpha.,5-Trimethyl-2-furanmethanol; 5-Ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-cis-2-furanmethanol; Furfuryl alcohol, tetrahydro-.alpha.,.alpha.,5-trimethyl-5-vinyl-; 2-Furanmethanol, 5-ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-; Z-2-Ethenyltetrahydro-.alpha.,.alpha.,5-trimethyl-furanmethanol; cis-2-Methyl-2-vinyl-5-(1-hydroxy-1-methylethyl)tetrahydrofuran; 2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-; Tetrahydro-2-methyl-5-(1-hydroxy-1-methylethyl)-2-vinylfuran; 5-Ethenyltetrahydro-alpha,alpha,5-trimethyl-2-furanmethanol; 2-((2R,5S)-5-Methyl-5-vinyltetrahydrofuran-2-yl)propan-2-ol; 5-(1-Hydroxy-1-methylethyl)-2-methyl-2-vinyltetrahydrofuran; 2-Methyl-2-vinyl-5-(1-hydroxy-1-methylethyl)tetrahydrofuran; Tetrahydro-alpha,alpha,5-trimethyl-5-vinylfuran-2-methanol; alpha,alpha,5-Trimethyl-5-vinyltetrahydrofurfuryl alcohol; 5-Ethenyltetrahydro-a,a,5-trimethyl-2-furanmethanol, 9CI; 2-Methyl-2-vinyl-5-(2-hydroxy-2-propyl)tetrahydrofuran; 2-(2-Hydroxy-2-propyl)-5-methyl-5-vinyltetrahydrofuran; 2-(5-Methyl-5-vinyltetrahydro-2-furanyl)-2-propanol #; 2-(5-Methyl-5-vinyltetrahydro-2-furanyl)-2-propanol; 2-(5-Methyl-5-vinyltetrahydrofuran-2-yl)propan-2-ol; 2-(Tetrahydro-5-methyl-5-vinyl-2-furyl)propan-2-ol; 2-(5-Methyl-5-vinyltetrahydro-1-furyl)-2-propanol; 2-(5-Methyl-5-vinyltetrahydro-2-furyl)-2-propanol; 2-(5-ETHENYL-5-METHYL-OXOLAN-2-YL)PROPAN-2-OL; 5-17-03-00253 (Beilstein Handbook Reference); 2-(5-ethenyl-5-methyloxolan-2-yl)propan-2-ol; 2-Furanmethanol,.alpha.,5-trimethyl-; 2,6-Dimethyl-3,6-oxido-7-oxten-2-ol; 2,6-Dimethyl-3,6-oxido-7-octen-2-ol; cis-Linalool oxide (furanoid form); cis-Linalool oxide (furanyl ring); Linalool oxide I (cis, furanoid); cis-Linalol oxide (furan isomer); cis-Linalool oxide (furan type); Linalool oxide B ((Z)-furanoid); Linalool oxide, natural, >=95\\%; (Z)-Linalool oxyde (furanoid); (Z)-Linalool oxide (furanoid); cis-linalool oxide (furanoid); Linalool oxide (cis-furanoid); cis-Linalyl oxide (furanoid); Linalool oxide, cis-furanoid; (Z)-Linalool oxide, furanoid; Z-Furanoid linalool oxide; cis-Furanic linalool oxid; cis-Furan linalool oxide; cis-Linalool furan oxide; Z-linalool oxide (furan); cis-Linalool oxide furan; (Z)-Furan linalool oxide; (Z)-Linalool furanoxide; cis-Linalool-3,6-oxide; cis-Linalol furanoxide; Furan linalool oxide; (Z)-Linalool oxide B; Linalool oxide, cis; Linalool 3,6-oxide; Linalool oxide B; Linolool oxide; Linalool oxide; Epoxylinalool; linalooloxide; Linalyl oxide; FEMA 3746; Linalool oxide



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

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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)

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

  • Emine Nur Herken, Ali Celik, Mustafa Aslan, Nilüfer Aydınlık. The constituents of essential oil: antimicrobial and antioxidant activity of Micromeria congesta Boiss. & Hausskn. ex Boiss. from East Anatolia. Journal of medicinal food. 2012 Sep; 15(9):835-9. doi: 10.1089/jmf.2011.0315. [PMID: 22871061]
  • Sol A Green, Xiuyin Chen, Niels J Nieuwenhuizen, Adam J Matich, Mindy Y Wang, Barry J Bunn, Yar-Khing Yauk, Ross G Atkinson. Identification, functional characterization, and regulation of the enzyme responsible for floral (E)-nerolidol biosynthesis in kiwifruit (Actinidia chinensis). Journal of experimental botany. 2012 Mar; 63(5):1951-67. doi: 10.1093/jxb/err393. [PMID: 22162874]
  • Mohammad Ali, Nisha Chaudhary. Ficus hispida Linn.: A review of its pharmacognostic and ethnomedicinal properties. Pharmacognosy reviews. 2011 Jan; 5(9):96-102. doi: 10.4103/0973-7847.79104. [PMID: 22096323]
  • M E Nehme, M A Keena, A Zhang, T C Baker, Z Xu, K Hoover. Evaluating the use of male-produced pheromone components and plant volatiles in two trap designs to monitor Anoplophora glabripennis. Environmental entomology. 2010 Feb; 39(1):169-76. doi: 10.1603/en09177. [PMID: 20146854]
  • Adam J Matich, Barry J Bunn, Martin B Hunt. The enantiomeric composition of linalool and linalool oxide in the flowers of kiwifruit (Actinidia) species. Chirality. 2010 Jan; 22(1):110-9. doi: 10.1002/chir.20713. [PMID: 19382237]
  • Jonas M Bengtsson, Yitbarek Wolde-Hawariat, Hamida Khbaish, Merid Negash, Bekele Jembere, Emiru Seyoum, Bill S Hansson, Mattias C Larsson, Ylva Hillbur. Field attractants for Pachnoda interrupta selected by means of GC-EAD and single sensillum screening. Journal of chemical ecology. 2009 Sep; 35(9):1063-76. doi: 10.1007/s10886-009-9684-7. [PMID: 19768509]
  • J M Sforcin, J T Amaral, A Fernandes, J P B Sousa, J K Bastos. Lemongrass effects on IL-1beta and IL-6 production by macrophages. Natural product research. 2009; 23(12):1151-9. doi: 10.1080/14786410902800681. [PMID: 19662581]
  • Umma Salma Jhumur, Stefan Dötterl, Andreas Jürgens. Floral odors of Silene otites: their variability and attractiveness to mosquitoes. Journal of chemical ecology. 2008 Jan; 34(1):14-25. doi: 10.1007/s10886-007-9392-0. [PMID: 18057987]
  • Jeong-Ok Kong, Il-Kwbon Park, Kwang-Sik Choi, Sang-Cheol Shin, Young-Joon Ahn. Nematicidal and Propagation Activities of Thyme Red and White Oil Compounds toward Bursaphelenchus xylophilus (Nematoda: Parasitaphelenchidae). Journal of nematology. 2007 Sep; 39(3):237-42. doi: . [PMID: 19259493]
  • Yu-Yun Hsiao, Wen-Chieh Tsai, Chang-Sheng Kuoh, Tian-Hsiang Huang, Hei-Chia Wang, Tian-Shung Wu, Yann-Lii Leu, Wen-Huei Chen, Hong-Hwa Chen. Comparison of transcripts in Phalaenopsis bellina and Phalaenopsis equestris (Orchidaceae) flowers to deduce monoterpene biosynthesis pathway. BMC plant biology. 2006 Jul; 6(?):14. doi: 10.1186/1471-2229-6-14. [PMID: 16836766]
  • Zheng-Zhu Zhang, Ying-Bo Li, Li Qi, Xiao-Chun Wan. Antifungal activities of major tea leaf volatile constituents toward Colletorichum camelliae Massea. Journal of agricultural and food chemistry. 2006 May; 54(11):3936-40. doi: 10.1021/jf060017m. [PMID: 16719518]
  • Andreas Jürgens, Stefan Dötterl. Chemical composition of anther volatiles in Ranunculaceae: genera-specific profiles in Anemone, Aquilegia, Caltha, Pulsatilla, Ranunculus, and Trollius species. American journal of botany. 2004 Dec; 91(12):1969-80. doi: 10.3732/ajb.91.12.1969. [PMID: 21652345]
  • Susanna Andersson, Heidi E M Dobson. Antennal responses to floral scents in the butterfly Heliconius melpomene. Journal of chemical ecology. 2003 Oct; 29(10):2319-30. doi: 10.1023/a:1026278531806. [PMID: 14682514]
  • Q Song, D Yang, G Zhang, C Yang. Volatiles from Ficus hispida and their attractiveness to fig wasps. Journal of chemical ecology. 2001 Oct; 27(10):1929-42. doi: 10.1023/a:1012226400586. [PMID: 11710602]