Lavandulol (BioDeep_00000895851)

   


代谢物信息卡片


4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, (theta)-

化学式: C10H18O (154.1357578)
中文名称: 熏衣草醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=CCC(CO)C(=C)C)C
InChI: InChI=1S/C10H18O/c1-8(2)5-6-10(7-11)9(3)4/h5,10-11H,3,6-7H2,1-2,4H3

描述信息

A monoterpenoid alcohol that is hepta-1-5-diene which is substituted at positions 2 and 6 by methyl groups and at position 3 by a hydroxymethyl group. It is commonly found in lavender oil.

同义名列表

16 个代谢物同义名

Lavandulol; 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, (theta)-; 4-Hexen-1-ol, 2-isopropenyl-5-methyl-, (-)- (8ci); 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, (R)-; (R)-5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol; (2R)-5-methyl-2-prop-1-en-2-yl-hex-4-en-1-ol; (2R)-5-methyl-2-prop-1-en-2-ylhex-4-en-1-ol; (2R)-2-isopropenyl-5-methyl-hex-4-en-1-ol; (2R)-2-isopropenyl-5-methylhex-4-en-1-ol; (-)-2-Isopropenyl-5-methyl-4-hexen-1-ol; (R)-(-)-Lavandulol; Lavandulol (6CI); (-)-lavandulol; (R)-lavandulol; 21090-68-6; 498-16-8



数据库引用编号

5 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。

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BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

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4 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

  • Hai-Wei Yan, Hui Zhu, Xiang Yuan, Ya-Nan Yang, Zi-Ming Feng, Jian-Shuang Jiang, Pei-Cheng Zhang. Eight new biflavonoids with lavandulyl units from the roots of Sophora flavescens and their inhibitory effect on PTP1B. Bioorganic chemistry. 2019 05; 86(?):679-685. doi: 10.1016/j.bioorg.2019.01.058. [PMID: 30831529]
  • Zerihun A Demissie, Lauren A E Erland, Mark R Rheault, Soheil S Mahmoud. The biosynthetic origin of irregular monoterpenes in Lavandula: isolation and biochemical characterization of a novel cis-prenyl diphosphate synthase gene, lavandulyl diphosphate synthase. The Journal of biological chemistry. 2013 Mar; 288(9):6333-41. doi: 10.1074/jbc.m112.431171. [PMID: 23306202]
  • S Siavash Saei-Dehkordi, Aziz A Fallah, S Saeid Saei-Dehkordi, Sanaz Kousha. Chemical composition and antioxidative activity of Echinophora platyloba DC. essential oil, and its interaction with natural antimicrobials against food-borne pathogens and spoilage organisms. Journal of food science. 2012 Nov; 77(11):M631-7. doi: 10.1111/j.1750-3841.2012.02956.x. [PMID: 23106123]
  • József Vuts, Zoltán Imrei, Miklós Töth. Development of an attractant-baited trap for Oxythyrea funesta Poda (Coleoptera: Scarabaeidae, Cetoniinae). Zeitschrift fur Naturforschung. C, Journal of biosciences. 2008 Sep; 63(9-10):761-8. doi: 10.1515/znc-2008-9-1023. [PMID: 19040118]
  • Hiroyuki Sakauchi, Hiromasa Kiyota, Shin-ya Takigawa, Takayuki Oritani, Shigefumi Kuwahara. Enzymatic resolution and odor description of both enantiomers of lavandulol, a fragrance of lavender oil. Chemistry & biodiversity. 2005 Sep; 2(9):1183-6. doi: 10.1002/cbdv.200590088. [PMID: 17193200]