2-hexadecynoic acid (BioDeep_00000607243)

   


代谢物信息卡片


2-hexadecynoic acid

化学式: C16H28O2 (252.20891880000002)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCCCCCCCCCCC#CC(=O)O
InChI: InChI=1S/C16H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-13H2,1H3,(H,17,18)

描述信息

同义名列表

1 个代谢物同义名

2-hexadecynoic acid



数据库引用编号

4 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)

0 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

  • Tatyana Savchenko, Evgeny Degtyaryov, Yaroslav Radzyukevich, Vlada Buryak. Therapeutic Potential of Plant Oxylipins. International journal of molecular sciences. 2022 Nov; 23(23):. doi: 10.3390/ijms232314627. [PMID: 36498955]
  • Chang Liu, Xiao-Tian Li, Rong-Rong Cheng, Zhu-Zhen Han, Li Yang, Zhong-Chen Song, Zheng-Tao Wang. Anti-oral common pathogenic bacterial active acetylenic acids from Thesium chinense Turcz. Journal of natural medicines. 2018 Mar; 72(2):433-438. doi: 10.1007/s11418-018-1180-3. [PMID: 29435792]
  • Ying Huang, Shuai-Bing Zhang, He-Ping Chen, Zhen-Zhu Zhao, Zheng-Hui Li, Tao Feng, Ji-Kai Liu. New acetylenic acids and derivatives from the Basidiomycete Craterellus lutescens (Cantharellaceae). Fitoterapia. 2016 Dec; 115(?):177-181. doi: 10.1016/j.fitote.2016.10.006. [PMID: 27773765]
  • Shoko Okada, Xue-Rong Zhou, Katherine Damcevski, Nerida Gibb, Craig Wood, Mats Hamberg, Victoria S Haritos. Diversity of Δ12 fatty acid desaturases in santalaceae and their role in production of seed oil acetylenic fatty acids. The Journal of biological chemistry. 2013 Nov; 288(45):32405-32413. doi: 10.1074/jbc.m113.511931. [PMID: 24062307]
  • Nobuwa Aoki, Kazuyuki Yamamoto, Takayuki Ogawa, Emi Ohta, Toshitaka Ikeuchi, Kazuo Kamemura, Susumu Ikegami, Shinji Ohta. Bromotheoynic acid, a brominated acetylenic acid from the marine sponge Theonella swinhoei. Natural product research. 2013; 27(2):117-22. doi: 10.1080/14786419.2012.660636. [PMID: 22324431]
  • Tao Xu, Siddharth K Tripathi, Qin Feng, Michael C Lorenz, Marsha A Wright, Melissa R Jacob, Melanie M Mask, Scott R Baerson, Xing-Cong Li, Alice M Clark, Ameeta K Agarwal. A potent plant-derived antifungal acetylenic acid mediates its activity by interfering with fatty acid homeostasis. Antimicrobial agents and chemotherapy. 2012 Jun; 56(6):2894-907. doi: 10.1128/aac.05663-11. [PMID: 22430960]
  • M-Y Yoon, G J Choi, Y H Choi, K S Jang, M S Park, B Cha, J-C Kim. Effect of polyacetylenic acids from Prunella vulgaris on various plant pathogens. Letters in applied microbiology. 2010 Nov; 51(5):511-7. doi: 10.1111/j.1472-765x.2010.02922.x. [PMID: 20849392]
  • I Stanish, A Singh. Highly stable vesicles composed of a new chain-terminus acetylenic photopolymeric phospholipid. Chemistry and physics of lipids. 2001 Aug; 112(2):99-108. doi: 10.1016/s0009-3084(01)00173-6. [PMID: 11551534]
  • G Zeni, R B Panatieri, E Lissner, P H Menezes, A L Braga, H A Stefani. Synthesis of polyacetylenic acids isolated from Heisteria acuminata. Organic letters. 2001 Mar; 3(6):819-21. doi: 10.1021/ol006946v. [PMID: 11263890]
  • D P Thewke, S R Panini, M Sinensky. Oleate potentiates oxysterol inhibition of transcription from sterol regulatory element-1-regulated promoters and maturation of sterol regulatory element-binding proteins. The Journal of biological chemistry. 1998 Aug; 273(33):21402-7. doi: 10.1074/jbc.273.33.21402. [PMID: 9694903]
  • N Tsevegsuren, W W Christie, D Lösel. Tanacetum (Chrysanthemum) corymbosum seed oil--a rich source of a novel conjugated acetylenic acid. Lipids. 1998 Jul; 33(7):723-7. doi: 10.1007/s11745-998-0262-2. [PMID: 9688176]