1-Nonadecanol (BioDeep_00000379385)

 

Secondary id: BioDeep_00000869603

PANOMIX_OTCML-2023


代谢物信息卡片


1-Nonadecanol; Nonadecyl alcohol; n-1-Nonadecanol; n-Nonadecanol

化学式: C19H40O (284.307899)
中文名称: 1-十九烷醇, 1-十九醇, 十九烷醇, 十九醇
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 43.9%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCCCO
InChI: InChI=1S/C19H40O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20/h20H,2-19H2,1H3

描述信息

A long-chain primary fatty alcohol that is nonadecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group.
1-Nonadecanol is a natural product found in Crataegus monogyna, Euphorbia piscatoria, and other organisms with data available.
1-Nonadecanol is one of the compositions of supercritical carbon dioxide (SC-CO2) essential oil of Heracleum thomsonii. 1-Nonadecanol is also an important aroma compound in Neotinea ustulata[1][2].
1-Nonadecanol is one of the compositions of supercritical carbon dioxide (SC-CO2) essential oil of Heracleum thomsonii. 1-Nonadecanol is also an important aroma compound in Neotinea ustulata[1][2].

同义名列表

16 个代谢物同义名

1-Nonadecanol; Nonadecyl alcohol; n-1-Nonadecanol; n-Nonadecanol; 1-Nonadecanol, European Pharmacopoeia (EP) Reference Standard; 1-hydroxynonadecane; 1-Nonadecanol, 99\\%; n-nonadecyl alcohol; Nonadecyl alcohol; n-1-nonadecanol; n-Nonadecanol-1; Nonadecanol-(1); Nonadecan-1-ol; n-Nonadecanol; 1-Nonadecanol; NONADECANOL; AI3-36471; C19H40O; 1-Nonadecanol



数据库引用编号

11 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(0)

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)

1 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

  • Ilaine T S Gehrke, Alexandre T Neto, Marcelo Pedroso, Clarice P Mostardeiro, Ivana B M Da Cruz, Ubiratan F Silva, Vinicius Ilha, Ionara I Dalcol, Ademir F Morel. Antimicrobial activity of Schinus lentiscifolius (Anacardiaceae). Journal of ethnopharmacology. 2013 Jul; 148(2):486-91. doi: 10.1016/j.jep.2013.04.043. [PMID: 23684720]
  • Gonzalo Obal, Ana Lía Ramos, Valeria Silva, Analía Lima, Carlos Batthyany, María Inés Bessio, Fernando Ferreira, Gustavo Salinas, Ana María Ferreira. Characterisation of the native lipid moiety of Echinococcus granulosus antigen B. PLoS neglected tropical diseases. 2012; 6(5):e1642. doi: 10.1371/journal.pntd.0001642. [PMID: 22616019]
  • Janine Hellenbrand, Eva-Maria Biester, Jens Gruber, Mats Hamberg, Margrit Frentzen. Fatty acyl-CoA reductases of birds. BMC biochemistry. 2011 Dec; 12(?):64. doi: 10.1186/1471-2091-12-64. [PMID: 22151413]
  • Mehdi Jalali-Heravi, Hadi Parastar, Heshmatollah Ebrahimi-Najafabadi. Characterization of volatile components of Iranian saffron using factorial-based response surface modeling of ultrasonic extraction combined with gas chromatography-mass spectrometry analysis. Journal of chromatography. A. 2009 Aug; 1216(33):6088-97. doi: 10.1016/j.chroma.2009.06.067. [PMID: 19595355]
  • Bin Li, Dong-Ming Zhang, Yong-Ming Luo. A new sesquiterpene lactone from the roots of Lasianthus acuminatissimus. Yao xue xue bao = Acta pharmaceutica Sinica. 2006 May; 41(5):426-30. doi: . [PMID: 16848318]
  • Anupam K Varshney, B Ravindra Babu, Ashok K Singh, Hari C Agarwal, Subhash C Jain. Ovipositional responses of Chilo partellus (Swinhoe) (Lepidoptera: pyralidae) to natural products from leaves of two maize (Zea mays L.) Cultivars. Journal of agricultural and food chemistry. 2003 Jul; 51(14):4008-12. doi: 10.1021/jf0211074. [PMID: 12822938]