Tricosane (BioDeep_00000011701)

 

Secondary id: BioDeep_00000631128, BioDeep_00000860039

human metabolite


代谢物信息卡片


CH3-[CH2]21-CH3

化学式: C23H48 (324.37558079999997)
中文名称: 二十三烷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCCCCCCC
InChI: InChI=1S/C23H48/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h3-23H2,1-2H3

描述信息

N-tricosane, also known as ch3-[ch2]21-ch3, is a member of the class of compounds known as alkanes. Alkanes are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. Thus, N-tricosane is considered to be a hydrocarbon lipid molecule. N-tricosane is an alkane and waxy tasting compound and can be found in a number of food items such as kohlrabi, papaya, coconut, and ginkgo nuts, which makes N-tricosane a potential biomarker for the consumption of these food products. N-tricosane can be found primarily in saliva. The term higher alkanes is sometimes used literally as "alkanes with a higher number of carbon atoms". One definition distinguishes the higher alkanes as the n-alkanes that are solid under natural conditions .
Tricosane belongs to the class of organic compounds known as acyclic alkanes. These are acyclic hydrocarbons consisting only of n carbon atoms and m hydrogen atoms where m=2*n + 2.

同义名列表

4 个代谢物同义名

CH3-[CH2]21-CH3; N-Triacosane; N-Tricosane; TRICOSANE



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

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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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PharmGKB(0)

135 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

  • Mayanka Walia, Tavleen S Mann, Dharmesh Kumar, Vijai K Agnihotri, Bikram Singh. Chemical Composition and In Vitro Cytotoxic Activity of Essential Oil of Leaves of Malus domestica Growing in Western Himalaya (India). Evidence-based complementary and alternative medicine : eCAM. 2012; 2012(?):649727. doi: 10.1155/2012/649727. [PMID: 22619691]
  • Ill-Min Chung, Hyung-In Moon. Immunotoxicity activity of 1,2,4-trimethoxybenzene from the Paulownia coreana Uyeki. against Aedes aegypti L. Immunopharmacology and immunotoxicology. 2011 Mar; 33(1):97-9. doi: 10.3109/08923973.2010.482591. [PMID: 20476845]
  • Ljuba Evstatieva, Milka Todorova, Daniela Antonova, Jordanka Staneva. Chemical composition of the essential oils of Rhodiola rosea L. of three different origins. Pharmacognosy magazine. 2010 Oct; 6(24):256-8. doi: 10.4103/0973-1296.71782. [PMID: 21120024]
  • Recep Kotan, Ahmet Cakir, Fatih Dadasoglu, Tuba Aydin, Ramazan Cakmakci, Hakan Ozer, Saban Kordali, Ebru Mete, Neslihan Dikbas. Antibacterial activities of essential oils and extracts of Turkish Achillea, Satureja and Thymus species against plant pathogenic bacteria. Journal of the science of food and agriculture. 2010 Jan; 90(1):145-60. doi: 10.1002/jsfa.3799. [PMID: 20355025]
  • Niko Radulović, Polina Blagojević, Radosav Palić. Fatty acid derived compounds--the dominant volatile class of the essential oil poor Sonchus arvensis subsp. uliginosus (Bieb.) Nyman. Natural product communications. 2009 Mar; 4(3):405-10. doi: ". [PMID: 19413122]
  • Mila Boncheva, Fabienne Damien, Valéry Normand. Molecular organization of the lipid matrix in intact Stratum corneum using ATR-FTIR spectroscopy. Biochimica et biophysica acta. 2008 May; 1778(5):1344-55. doi: 10.1016/j.bbamem.2008.01.022. [PMID: 18298945]
  • Jules-Roger Kuiate, Jean Marie Bessière, Paul Henri Amvam Zollo, Serge Philibert Kuate. Chemical composition and antidermatophytic properties of volatile fractions of hexanic extract from leaves of Cupressus lusitanica Mill. from Cameroon. Journal of ethnopharmacology. 2006 Jan; 103(2):160-5. doi: 10.1016/j.jep.2005.07.022. [PMID: 16169171]
  • Robert J Bartelt, Allard A Cossé, Richard J Petroski, David K Weaver. Cuticular hydrocarbons and novel alkenediol iacetates from wheat stem sawfly (Cephus cinctus): natural oxidation to pheromone components. Journal of chemical ecology. 2002 Feb; 28(2):385-405. doi: 10.1023/a:1017994410538. [PMID: 11925075]