2-Hydroxyhexadecanoic acid (BioDeep_00000022558)

 

Secondary id: BioDeep_00000593365

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


(2S)-2-Hydroxyhexadecanoic acid

化学式: C16H32O3 (272.2351322)
中文名称: (±)-2-羟基十六烷酸, 2-羟基十六烷酸
谱图信息: 最多检出来源 Viridiplantae(plant) 6.53%

Reviewed

Last reviewed on 2024-09-13.

Cite this Page

2-Hydroxyhexadecanoic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/2-hydroxyhexadecanoic_acid (retrieved 2024-09-18) (BioDeep RN: BioDeep_00000022558). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: CCCCCCCCCCCCCCC(C(=O)O)O
InChI: InChI=1S/C16H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15,17H,2-14H2,1H3,(H,18,19)

描述信息

2-Hydroxyhexadecanoic acid (CAS: 764-67-0), also known as 2-hydroxypalmitic acid, is a member of the class of compounds known as long-chain fatty acids. Long-chain fatty acids are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. The chain of 2-hydroxyhexadecanoic acid bears a hydroxyl group. 2-Hydroxyhexadecanoic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). 2-Hydroxyhexadecanoic acid occurs in wool fat, which is used as a chewing gum softener.
2-Hydroxypalmitic acid is an intermediate in phytosphingosine metabolism[1].

同义名列表

44 个代谢物同义名

(2S)-2-Hydroxyhexadecanoic acid; (S)-alpha-Hydroxypalmitic acid; (S)-2-Hydroxyhexadecanoic acid; (±)-alpha-hydroxypalmitic acid; alpha-Hydroxyhexadecanoic acid; (±)-2-hydroxyhexadecanoic acid; DL-2-Hydroxyhexadecanoic acid; L-2-Hydroxyhexadecanoic acid; (2S)-2-Hydroxyhexadecanoate; 2S-hydroxyhexadecanoic acid; (S)-Α-hydroxypalmitic acid; 2-Hydroxyhexadecanoic acid; Α-hydroxyhexadecanoic acid; (S)-alpha-Hydroxypalmitate; alpha-Hydroxypalmitic acid; alpha-Hydroxyhexadecanoate; (S)-2-Hydroxypalmitic acid; (±)-2-hydroxyhexadecanoate; (±)-α-hydroxypalmitic acid; (±)-alpha-hydroxypalmitate; (S)-2-Hydroxyhexadecanoate; DL-2-Hydroxyhexadecanoate; DL-2-Hydroxypalmitic acid; L-2-Hydroxypalmitic acid; L-2-Hydroxyhexadecanoate; 2S-Hydroxyhexadecanoate; 2S-hydroxypalmitic acid; 2-hydroxy Palmitic Acid; Α-hydroxyhexadecanoate; 2-Hydroxyhexadecanoate; alpha-Hydroxypalmitate; (S)-Α-hydroxypalmitate; 2-Hydroxypalmitic acid; (±)-α-hydroxypalmitate; (S)-2-Hydroxypalmitate; Α-hydroxypalmitic acid; DL-2-Hydroxypalmitate; L-2-Hydroxypalmitate; 2S-Hydroxypalmitate; Α-hydroxypalmitate; 2-Hydroxypalmitate; FA(16:0(2S-OH)); FA(16:0(2-OH)); (S)-2OH PA



数据库引用编号

10 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(4)

BioCyc(0)

PlantCyc(0)

代谢反应

56 个相关的代谢反应过程信息。

Reactome(56)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

15 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

  • Hiroyuki Fukami, Hideki Tachimoto, Mikiya Kishi, Takayuki Kaga, Hatsue Waki, Machiko Iwamoto, Yasukazu Tanaka. Preparation of (13)C-labeled ceramide by acetic acid bacteria and its incorporation in mice. Journal of lipid research. 2010 Nov; 51(11):3389-95. doi: 10.1194/jlr.d009191. [PMID: 20656918]
  • Lin Guo, Dequan Zhou, Kenneth M Pryse, Adewole L Okunade, Xiong Su. Fatty acid 2-hydroxylase mediates diffusional mobility of Raft-associated lipids, GLUT4 level, and lipogenesis in 3T3-L1 adipocytes. The Journal of biological chemistry. 2010 Aug; 285(33):25438-47. doi: 10.1074/jbc.m110.119933. [PMID: 20519515]
  • Soon Dong Lee, Se Jae Kim. Aeromicrobium tamlense sp. nov., isolated from dried seaweed. International journal of systematic and evolutionary microbiology. 2007 Feb; 57(Pt 2):337-341. doi: 10.1099/ijs.0.64442-0. [PMID: 17267975]
  • K D Cox, H Scherm, M B Riley. Characterization of Armillaria spp. from peach orchards in the southeastern United States using fatty acid methyl ester profiling. Mycological research. 2006 Apr; 110(Pt 4):414-22. doi: 10.1016/j.mycres.2005.12.004. [PMID: 16546364]
  • N Takakuwa, K Saito, M Ohnishi, Y Oda. Determination of glucosylceramide contents in crop tissues and by-products from their processing. Bioresource technology. 2005 Jun; 96(9):1089-92. doi: 10.1016/j.biortech.2004.09.019. [PMID: 15668206]
  • L D Varbanets, V N Vasil'ev, O S Brovarskaia. [Characterization of lipopolysaccharides from Ralstonia solanacearum]. Mikrobiologiia. 2003 Jan; 72(1):19-25. doi: ". [PMID: 12698787]
  • K M Koshy, J M Boggs. Partial synthesis and physical properties of cerebroside sulfate containing palmitic acid or alpha-hydroxy palmitic acid. Chemistry and physics of lipids. 1983 Dec; 34(1):41-53. doi: 10.1016/0009-3084(83)90058-0. [PMID: 6661805]