1-Heptadecanol (BioDeep_00000397374)

 

Secondary id: BioDeep_00000863846

PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


60EE1D22-0C43-4AEE-B6F6-FBD44178F59F

化学式: C17H36O (256.2766006)
中文名称: 十七醇, 1-十七烷醇
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 73.17%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCO
InChI: InChI=1S/C17H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h18H,2-17H2,1H3

描述信息

Heptadecan-1-ol is a long-chain fatty alcohol that is heptadecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group. It has a role as a plant metabolite. It is a long-chain primary fatty alcohol and a primary alcohol.
1-Heptadecanol is a natural product found in Euphorbia piscatoria, Phyllanthus emblica, and other organisms with data available.
A long-chain primary fatty alcohol that is heptadecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group.
1-heptadecanol, also known as 1-hydroxyheptadecane or heptadecyl alcohol, is a member of the class of compounds known as long-chain fatty alcohols. Long-chain fatty alcohols are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. 1-heptadecanol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 1-heptadecanol can be found in black elderberry and potato, which makes 1-heptadecanol a potential biomarker for the consumption of these food products.
1-Heptadecanol is a long-chain primary alcohol with antibacterial activity from Solena amplexicaulis leaves[1].
1-Heptadecanol is a long-chain primary alcohol with antibacterial activity from Solena amplexicaulis leaves[1].

同义名列表

18 个代谢物同义名

60EE1D22-0C43-4AEE-B6F6-FBD44178F59F; 1-Heptadecanol, purum, >=97.0\\% (GC); 1-Heptadecanol, 98\\%; 1-Hydroxyheptadecane; n-heptadecyl alcohol; HEPTADECYL ALCOHOL; HEPTADECANOL, 1-; n-Heptadecanol-1; MARGARIC ALCOHOL; Heptadecan-1-ol; UNII-N3IL85TMCX; n-Heptadecanol; 1-Heptadecanol; Tox21_303960; Heptadecanol; N3IL85TMCX; AI3-01234; 1-Heptadecanol



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)

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

  • 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]
  • Igor Jerković, Zvonimir Marijanović, I Ljubicić, M Gugić. Contribution of the bees and combs to honey volatiles: blank-trial probe for chemical profiling of honey biodiversity. Chemistry & biodiversity. 2010 May; 7(5):1217-30. doi: 10.1002/cbdv.200900100. [PMID: 20491078]
  • Yusuke Miyajima, Hiroyuki Nakamura, Yasuhiro Kuwata, Jong-Dae Lee, Shinichiro Masunaga, Koji Ono, Kazuo Maruyama. Transferrin-loaded nido-carborane liposomes: tumor-targeting boron delivery system for neutron capture therapy. Bioconjugate chemistry. 2006 Sep; 17(5):1314-20. doi: 10.1021/bc060064k. [PMID: 16984142]
  • Hiroyuki Nakamura, Yusuke Miyajima, Toshiaki Takei, Satoshi Kasaoka, Kazuo Maruyama. Synthesis and vesicle formation of a nido-carborane cluster lipid for boron neutron capture therapy. Chemical communications (Cambridge, England). 2004 Sep; ?(17):1910-1. doi: 10.1039/b406141a. [PMID: 15340596]
  • 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]
  • H S Seo, Y Endo, M Moku, K Kawaguchi, K Fujimoto. Wax ester biosynthesis in the liver of myctophid fishes. Lipids. 2001 Apr; 36(4):389-93. doi: 10.1007/s11745-001-0733-5. [PMID: 11383691]
  • L Giuliani, G Carmignani, E Belgrano, P Puppo. Transcatheter arterial embolization in urological tumors: the use of isobutyl-2-cyanoacrylate. The Journal of urology. 1979 May; 121(5):630-4. doi: 10.1016/s0022-5347(17)56913-x. [PMID: 439260]
  • P Hernuss, E Müller Tyl, H Salzer, H Sinzinger, L Wicke, T Prey, L Reisinger. [Pollen diet as an adjuvans of radiotherapy in gynecologic carcinomas]. Strahlentherapie. 1975 Nov; 150(5):500-6. doi: NULL. [PMID: 2995]