epsilon-Tocopherol (BioDeep_00000019372)

 

Secondary id: BioDeep_00000004130, BioDeep_00001871983

human metabolite Endogenous Volatile Flavor Compounds


代谢物信息卡片


(2R)-3,4-dihydro-2,5,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-2H-1-benzopyran-6-ol

化学式: C28H42O2 (410.3184632)
中文名称: 生育三烯酚
谱图信息: 最多检出来源 Homo sapiens(feces) 3.02%

分子结构信息

SMILES: CC(C)=CCCC(C)=CCCC(C)=CCCC1(C)CCc2c(C)c(O)cc(C)c2O1
InChI: InChI=1S/C28H42O2/c1-20(2)11-8-12-21(3)13-9-14-22(4)15-10-17-28(7)18-16-25-24(6)26(29)19-23(5)27(25)30-28/h11,13,15,19,29H,8-10,12,14,16-18H2,1-7H3/b21-13+,22-15+

描述信息

Isolated from wheat bran oil. epsilon-Tocopherol is found in many foods, some of which are rye, coconut, rosemary, and fennel.
epsilon-Tocopherol is found in american cranberry. epsilon-Tocopherol is isolated from wheat bran oi

同义名列表

15 个代谢物同义名

(2R)-3,4-dihydro-2,5,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-2H-1-benzopyran-6-ol; 2,5,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-1-benzopyran-6-ol; 2,5,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-1-benzopyran-6-ol; 2R,5,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-chromen-6-ol; 3,4-dihydro-2,5,8-Trimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-4H-1-benzopyran-6-ol, 9ci; .epsilon.-Tocopherol; (-)-beta-Tocotrienol; epsilon-tocopherol; D-beta-Tocotrienol; epsilon-Tokoferol; Tocotrienol, beta; beta-tocotrienol; e-Tocopherol; e-Tokoferol; beta-Tocotrienol



数据库引用编号

17 个数据库交叉引用编号

分类词条

相关代谢途径

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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)

7 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

  • Emily J Watts, Yu Shen, Ephraim P Lansky, Eviatar Nevo, Gerd Bobe, Maret G Traber. High environmental stress yields greater tocotrienol content while changing vitamin e profiles of wild emmer wheat seeds. Journal of medicinal food. 2015 Feb; 18(2):216-23. doi: 10.1089/jmf.2014.0017. [PMID: 25105230]
  • Kazuo Mukai, Eri Ishikawa, Aya Ouchi, Shin-Ichi Nagaoka, Tomomi Suzuki, Katsuhiro Izumisawa, Taisuke Koike. Kinetic study of the quenching reaction of singlet oxygen by α-, β-, γ-, δ-tocotrienols, and palm oil and soybean extracts in solution. Bioscience, biotechnology, and biochemistry. 2014; 78(12):2089-101. doi: 10.1080/09168451.2014.943653. [PMID: 25093256]
  • Daniela de Oliveira Ribeiro, Bianca Waruar Lobo, Nádia Maria Volpato, Venício Féo da Veiga, Lúcio Mendes Cabral, Valeria Pereira de Sousa. Influence of the calcium concentration in the presence of organic phosphorus on the physicochemical compatibility and stability of all-in-one admixtures for neonatal use. Nutrition journal. 2009 Oct; 8(?):51. doi: 10.1186/1475-2891-8-51. [PMID: 19857269]
  • Chisato Abe, Saiko Ikeda, Tomono Uchida, Kanae Yamashita, Tomio Ichikawa. Triton WR1339, an inhibitor of lipoprotein lipase, decreases vitamin E concentration in some tissues of rats by inhibiting its transport to liver. The Journal of nutrition. 2007 Feb; 137(2):345-50. doi: 10.1093/jn/137.2.345. [PMID: 17237309]
  • H Nakamura, F Furukawa, A Nishikawa, M Miyauchi, H Y Son, T Imazawa, M Hirose. Oral toxicity of a tocotrienol preparation in rats. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2001 Aug; 39(8):799-805. doi: 10.1016/s0278-6915(01)00025-4. [PMID: 11434987]
  • T M Black, P Wang, N Maeda, R A Coleman. Palm tocotrienols protect ApoE +/- mice from diet-induced atheroma formation. The Journal of nutrition. 2000 Oct; 130(10):2420-6. doi: 10.1093/jn/130.10.2420. [PMID: 11015467]
  • E Katsanidis, P B Addis. Novel HPLC analysis of tocopherols, tocotrienols, and cholesterol in tissue. Free radical biology & medicine. 1999 Dec; 27(11-12):1137-40. doi: 10.1016/s0891-5849(99)00205-1. [PMID: 10641704]
  • B C Pearce, R A Parker, M E Deason, D D Dischino, E Gillespie, A A Qureshi, K Volk, J J Wright. Inhibitors of cholesterol biosynthesis. 2. Hypocholesterolemic and antioxidant activities of benzopyran and tetrahydronaphthalene analogues of the tocotrienols. Journal of medicinal chemistry. 1994 Feb; 37(4):526-41. doi: 10.1021/jm00030a012. [PMID: 8120870]
  • V Piironen, P Varo, E L Syväoja, K Salminen, P Koivistoinen. High-performance liquid chromatographic determination of tocopherols and tocotrienols and its application to diets and plasma of Finnish men. I. Analytical method. International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition. 1984; 54(1):35-40. doi: . [PMID: 6735614]