Methyl stearate (BioDeep_00000017479)

 

Secondary id: BioDeep_00000418819, BioDeep_00000860890

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


InChI=1/C19H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h3-18H2,1-2H

化学式: C19H38O2 (298.28716479999997)
中文名称: 硬脂酸甲酯
谱图信息: 最多检出来源 Homo sapiens(lipidomics) 6.13%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCC(=O)OC
InChI: InChI=1S/C19H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h3-18H2,1-2H3

描述信息

Methyl stearate appears as white crystals or chunky solid. (NTP, 1992)
Methyl stearate is a fatty acid methyl ester and an octadecanoate ester. It has a role as a metabolite.
Methyl stearate is a natural product found in Cinnamomum kotoense, Hedysarum polybotrys, and other organisms with data available.
A fatty acid methyl ester obtained by formal condensation of the carboxy group of octadecanoic (stearic) acid with the hydroxy group of methanol. A natural product found in Neolitsea daibuensis.
Antifoaming agent and fermentation nutrient. Methyl stearate is found in cloves.
Methyl stearate is found in cloves. Antifoaming agent and fermentation nutrient.
Methyl stearate, isolated from Rheum palmatum L. is a compopent of of soybean and rapeseed biodiesels[1].
Methyl stearate, isolated from Rheum palmatum L. is a compopent of of soybean and rapeseed biodiesels[1].

同义名列表

50 个代谢物同义名

InChI=1/C19H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h3-18H2,1-2H; Methyl Stearate; Octadecanoic acid methyl ester; Methyl octadecanoate; Methyl stearate, United States Pharmacopeia (USP) Reference Standard; Methyl stearate, European Pharmacopoeia (EP) Reference Standard; Methyl stearate, certified reference material, TraceCERT(R); 4-METHOXY-BENZENECARBODITHIOICACIDMETHYLESTER; 4-02-00-01216 (Beilstein Handbook Reference); methyl stearate [standard material for gc]; Octadecanoic acid methyl ester (FAME MIX); Methyl stearate, analytical standard; 6A62CF35-4D1C-47C0-8186-CAB436C59C3F; n-Octadecanoic acid, methyl ester; Methyl ester of octadecanoic acid; n-Octadecanoic acid methyl ester; n-Octadecanoic acid methyl ester; Octadecanoic acid, methyl ester; OCTADECANOIC ACID,METHYL ESTER; octadecanoic acid methyl ester; Octadecanoic acid-methyl ester; STEARIC ACID METHYL ESTER [MI]; Methyl stearate, >=96\\%, FG; Methyl stearate, ~99\\% (GC); Methyl (Z)-9-octadecenoate; Stearic acid, methyl ester; Stearic acid methyl ester; METHYL STEARATE [USP-RS]; Methyl octadecanoic acid; METHYL STEARATE (USP-RS); METHYL STEARATE [INCI]; METHYL STEARATE [HSDB]; Methyl n-octadecanoate; Methyl Stearate-1-13C; METHYL STEARATE (II); METHYL STEARATE [II]; Methyl octadecanoate; Methyl stearic acid; Methyl-d3Stearate; UNII-8D4NXF3ZH7; Methyl stearate; Metholene 2218; METHYLSTEARATE; Kemester 9718; Kemester 4516; Kemester 9018; WE(1:0/18:0); WLN: 17VO1; 8D4NXF3ZH7; AI3-07960; SFE 19:0; C18 FAME



数据库引用编号

13 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)

50 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

  • Lu Han, Zijian Xu, Jianhua Huang, Zong Meng, Yuanfa Liu, Xingguo Wang. Enzymatically catalyzed synthesis of low-calorie structured lipid in a solvent-free system: optimization by response surface methodology. Journal of agricultural and food chemistry. 2011 Dec; 59(23):12635-42. doi: 10.1021/jf2029658. [PMID: 22082136]
  • Marie Trabalon. Agonistic interactions, cuticular and hemolymphatic lipid variations during the foraging period in spider females Brachypelma albopilosa (Theraphosidae). Journal of insect physiology. 2011 Jun; 57(6):735-43. doi: 10.1016/j.jinsphys.2011.02.011. [PMID: 21338607]
  • Penglin Li, Xiaoling Miao, Rongxiu Li, Jianjiang Zhong. In situ biodiesel production from fast-growing and high oil content Chlorella pyrenoidosa in rice straw hydrolysate. Journal of biomedicine & biotechnology. 2011; 2011(?):141207. doi: 10.1155/2011/141207. [PMID: 21318171]
  • Muchtaridi, Anas Subarnas, Anton Apriyantono, Resmi Mustarichie. Identification of compounds in the essential oil of nutmeg seeds (Myristica fragrans Houtt.) that inhibit locomotor activity in mice. International journal of molecular sciences. 2010 Nov; 11(11):4771-81. doi: 10.3390/ijms11114771. [PMID: 21151471]
  • Ru Yang, Mengxing Su, Min Li, Jianchun Zhang, Xinmin Hao, Hua Zhang. One-pot process combining transesterification and selective hydrogenation for biodiesel production from starting material of high degree of unsaturation. Bioresource technology. 2010 Aug; 101(15):5903-9. doi: 10.1016/j.biortech.2010.02.095. [PMID: 20231090]
  • María Ayelén Pagani, Miguel A Baltanás. Production of natural antioxidants from vegetable oil deodorizer distillates: effect of catalytic hydrogenation. Bioresource technology. 2010 Feb; 101(4):1369-76. doi: 10.1016/j.biortech.2009.09.068. [PMID: 19833504]
  • Shao-Hui Zhu, Qian-Jun Zhang, Qing Chen, Tuo Zhou, Rong-Jun Yao. [Study on the chemical constituents of Dichrocephala integrifolia]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2010 Jan; 33(1):53-5. doi: . [PMID: 20518304]
  • Martin Frenkel, Carsten Külheim, Hanna Johansson Jänkänpää, Oskar Skogström, Luca Dall'Osto, Jon Agren, Roberto Bassi, Thomas Moritz, Jon Moen, Stefan Jansson. Improper excess light energy dissipation in Arabidopsis results in a metabolic reprogramming. BMC plant biology. 2009 Jan; 9(?):12. doi: 10.1186/1471-2229-9-12. [PMID: 19171025]
  • Lei Guo, Guo Qing Li. Olfactory perception of oviposition-deterring fatty acids and their methyl esters by the Asian corn borer, Ostrinia furnacalis. Journal of insect science (Online). 2009; 9(?):1-9. doi: 10.1673/031.009.6701. [PMID: 20053122]
  • Jorge Luiz Vieira dos Anjos, Diógenes de Sousa Neto, Antonio Alonso. Effects of ethanol/l-menthol on the dynamics and partitioning of spin-labeled lipids in the stratum corneum. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V. 2007 Sep; 67(2):406-12. doi: 10.1016/j.ejpb.2007.02.004. [PMID: 17350812]
  • George F Antonious, Janet E Meyer, Jami A Rogers, Yoon-Hyeon Hu. Growing hot pepper for cabbage looper, Trichopulsia ni (Hübner) and spider mite, Tetranychus urticae (Koch) control. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2007 Jun; 42(5):559-67. doi: 10.1080/03601230701389512. [PMID: 17562464]
  • Zhorro S Nickolov, David W Britt, Jan D Miller. Sum-frequency spectroscopy analysis of two-component langmuir monolayers and the associated interfacial water structure. The journal of physical chemistry. B. 2006 Aug; 110(31):15506-13. doi: 10.1021/jp0631578. [PMID: 16884274]
  • Miguel Clemente-León, Eugenio Coronado, Alejandra Soriano-Portillo, Enrique Colacio, José M Domínguez-Vera, Natividad Galvez, Rafael Madueño, María T Martín-Romero. Magnetic Langmuir-Blodgett films of ferritin with different iron contents. Langmuir : the ACS journal of surfaces and colloids. 2006 Aug; 22(16):6993-7000. doi: 10.1021/la061284p. [PMID: 16863250]
  • J Kapuśniak, P Tomasik. Lipid microencapsulation in starch. Journal of microencapsulation. 2006 May; 23(3):341-8. doi: 10.1080/02652040600687571. [PMID: 16801245]
  • Harshil Dhruv, Revathi Pepalla, Mundeta Taveras, David W Britt. Protein insertion and patterning of PEG bearing langmuir monolayers. Biotechnology progress. 2006 Jan; 22(1):150-5. doi: 10.1021/bp050173y. [PMID: 16454505]
  • Pekka Vähäoja, Jani Närhi, Toivo Kuokkanen, Outi Naatus, Jorma Jalonen, Sulo Lahdelma. An infrared spectroscopic method for quantitative analysis of fatty alcohols and fatty acid esters in machinery oils. Analytical and bioanalytical chemistry. 2005 Sep; 383(2):305-11. doi: 10.1007/s00216-005-3405-z. [PMID: 16132128]
  • Thomas Goodman, Ezra Bussmann, Clayton Williams, Mundeta Taveras, David Britt. Electrostatic force microscopy analysis of lipid miscibility in two-component monolayers. Langmuir : the ACS journal of surfaces and colloids. 2004 Apr; 20(9):3684-9. doi: 10.1021/la036366h. [PMID: 15875400]
  • Ahmet C Gören, Gökhan Bilsel, Mehmet Altun, Fatih Satil, Tuncay Dirmenci. Fatty acid composition of seeds of Satureja thymbra and S. cuneifolia. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2003 Jul; 58(7-8):502-4. doi: 10.1515/znc-2003-7-810. [PMID: 12939035]
  • B H Chen, Y C Chen. Formation of polycyclic aromatic hydrocarbons in the smoke from heated model lipids and food lipids. Journal of agricultural and food chemistry. 2001 Nov; 49(11):5238-43. doi: 10.1021/jf0106906. [PMID: 11714310]
  • 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]