alpha-fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol (BioDeep_00000228620)

Main id: BioDeep_00000004901

 

human metabolite


代谢物信息卡片


alpha-fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol

化学式: C10H18O (154.1357578)
中文名称: 溶剂红172
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1(C)[C@@H]2CC[C@@](C)(C2)[C@@H]1O
InChI: InChI=1S/C10H18O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1

描述信息

Fenchol or 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchol is a naturally occurring bicyclic monoterpenoid and an isomer of Borneol. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-eritritol-phosphate (MEP) pathway in the plastids. Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclation reactions to yield a diverse number of cyclic arrangements. Fenchol is an extremely weak basic (essentially neutral) compound (based on its pKa). It is a colorless or white solid with a characteristic scent found in basil and Aster. Fenchol is used extensively in perfumery.
Flavouring compound [Flavornet]

同义名列表

43 个代谢物同义名

alpha-fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol; rel-(1R,2R,4S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol; a-Fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol; Α-fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol; (1S,2S,4R)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol; (1S,2-endo)-1,3,3-Trimethylnorbornan-2-ol; 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol; 1,3,3-trimethyl-2-norbornanol; fenchol, ((endo)-(+-))-isomer; fenchol, ((exo)-(+-))-isomer; (-)-alpha-Fenchyl alcohol; fenchol, (1S-endo)-isomer; fenchol, (1R-endo)-isomer; fenchol, (1S-exo)-isomer; l-alpha-Fenchyl alcohol; (1S,2S,4R)-endo-Fenchol; fenchol, (endo)-isomer; fenchol, (exo)-isomer; alpha-Fenchyl alcohol; (-)-a-Fenchyl alcohol; ((endo)-(+-))-fenchol; (-)-Α-fenchyl alcohol; l-α-Fenchyl alcohol; endo-alpha-Fenchol; (±)-alpha-Fenchol; (-)-alpha-fenchol; a-Fenchyl alcohol; Α-fenchyl alcohol; (1S-endo)-Fenchol; (-)-endo-Fenchol; dl-alpha-Fenchol; Fenchyl alcohol; endo-a-Fenchol; endo-Α-fenchol; (-)-α-Fenchol; alpha-Fenchol; (±)-α-Fenchol; endo-fenchol; dl-α-Fenchol; 2-Fenchanol; a-Fenchol; Α-fenchol; Fenchol



数据库引用编号

15 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(2)

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)

30 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

  • Mohamed Salim, T K Ahmedul Kabeer, S Ajikumaran Nair, Mathew Dan, M Sabu, Sabulal Baby. Chemical profile, antiproliferative and antioxidant activities of rhizome oil of Zingiber anamalayanum from Western Ghats in India. Natural product research. 2016 Sep; 30(17):1965-8. doi: 10.1080/14786419.2015.1094802. [PMID: 26456637]
  • Rajendra C Padalia, Ram S Verma, Velusamy Sundaresan, Chandan S Chanotiya. Chemical diversity in the genus Alpinia (Zingiberaceae): comparative composition of four Alpinia species grown in Northern India. Chemistry & biodiversity. 2010 Aug; 7(8):2076-87. doi: 10.1002/cbdv.201000013. [PMID: 20730971]
  • Rajendra C Padalia, Chandan S Chanotiya, V Sundaresan. Compositional variability in essential oil from different parts of Alpinia speciosa from India. Natural product communications. 2010 Feb; 5(2):279-82. doi: . [PMID: 20334144]
  • D Yang, F Wang, J Peng, S Ren. [GC-MS analysis and inhibitory activity of the essential oil extracted from the leaves of Lindera communis]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 1999 Mar; 22(3):128-31. doi: ". [PMID: 12575094]