Pseudoionone (BioDeep_00000024306)

   

human metabolite Endogenous natural product


代谢物信息卡片


N-[2-(1-Aziridinyl)ethyl]-3,7-dimethyl-6-octen-1-amine

化学式: C13H20O (192.1514)
中文名称: 假紫罗兰酮, 6,10-二甲基-3，5，9-十一三烯-2-酮, (E)-ψ-紫罗兰酮
谱图信息: 最多检出来源 Viridiplantae(plant) 10.34%

分子结构信息

SMILES: CC(=CCCC(=CC=CC(=O)C)C)C
InChI: InChI=1S/C13H20O/c1-11(2)7-5-8-12(3)9-6-10-13(4)14/h6-7,9-10H,5,8H2,1-4H3/b10-6+,12-9+

描述信息

Pseudoionone (CAS: 141-10-6), also known as citrylideneacetone or psi-ionone, belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. Pseudoionone is an extremely weak basic (essentially neutral) compound (based on its pKa). Pseudoionone is a sweet, balsamic, and citrus tasting compound. Outside of the human body, pseudoionone has been detected, but not quantified in, a few different foods, such as cherry tomato and garden tomato. This could make pseudoionone a potential biomarker for the consumption of these foods. Pseudoionone is used as a food additive (EAFUS: Everything Added to Food in the United States).
It is used as a food additive .

同义名列表

37 个代谢物同义名

N-[2-(1-Aziridinyl)ethyl]-3,7-dimethyl-6-octen-1-amine; (3E,5E)-6,10-Dimethylundeca-3,5,9-trien-2-one; 8-[N-aziridylethylamino]-2,6-Dimethyloctene-2; (3E,5E)-6,10-Dimethyl-3,5,9-undecatrien-2-one; (E,E)-6,10-Dimethyl-3,5,9-undecatrien-2-one; 6,10-Dimethyl-(e,e)-3,5,9-undecatrien-2-one; 3,5,9-Undecatrien-2-one, 6,10-dimethyl, #3; 3,5,9-Undecatrien-2-one, 6,10-dimethyl, #1; 3,5,9-Undecatrien-2-one, 6,10-dimethyl, #2; 2,6-Dimethyl hendeca-2,6,8-trien-10-one; 6,10-Dimethyl-3,5,9-undecatriene-2-one; 2,6-Dimethylundeca-2,6,8-triene-10-one; 2,6-Dimethylhendeca-2,6,8-trien-10-one; 2,6-Dimethyl-2,6,8-undecatrien-10-one; 6,10-Dimethylundeca-3,5,9-trien-2-one; 6,10-Dimethyl-3,5,9-undecatrien-2-one; trans,trans-Pseudoionone; laquo psiraquo -Ionone; (E,E)-Pseudoionone; 3E,5E-Pseudoionone; Citrylideneacetone; trans-.psi.-ionone; (all-E)-psi-Ionone; (all-E)-ψ-Ionone; trans-psi-Ionone; 2-Pseudoionone; trans-ψ-Ionone; Pseudoionones; 2-Pseudojonon; .psi.-ionone; Pseudoionone; phi-Ionone; psi-Ionone; ψ-Ionone; φ-Ionone; Pseudoionone; Pseudoionone



数据库引用编号

12 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

代谢反应

170 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(2)

  • carotenoid cleavage: β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial
  • carotenoid cleavage: all-trans-β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial

WikiPathways(0)

Plant Reactome(163)

INOH(0)

PlantCyc(5)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

21 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。

亚细胞结构定位 关联基因列表


文献列表

  • Fawzia H Abdel-Rahman, Nina M Alaniz, Mahmoud A Saleh. Nematicidal activity of terpenoids. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2013; 48(1):16-22. doi: 10.1080/03601234.2012.716686. [PMID: 23030436]
  • N L Rodríguez-Ávila, J A Narváez-Zapata, J E Ramírez-Benítez, M L Aguilar-Espinosa, R Rivera-Madrid. Identification and expression pattern of a new carotenoid cleavage dioxygenase gene member from Bixa orellana. Journal of experimental botany. 2011 Nov; 62(15):5385-95. doi: 10.1093/jxb/err201. [PMID: 21813796]
  • Federica Brandi, Einat Bar, Fabienne Mourgues, Györgyi Horváth, Erika Turcsi, Giovanni Giuliano, Alessandro Liverani, Stefano Tartarini, Efraim Lewinsohn, Carlo Rosati. Study of 'Redhaven' peach and its white-fleshed mutant suggests a key role of CCD4 carotenoid dioxygenase in carotenoid and norisoprenoid volatile metabolism. BMC plant biology. 2011 Jan; 11(?):24. doi: 10.1186/1471-2229-11-24. [PMID: 21269483]
  • Ester Innocent, Cosam C Joseph, Nicholas K Gikonyo, Mayunga H H Nkunya, Ahmed Hassanali. Constituents of the essential oil of Suregada zanzibariensis leaves are repellent to the mosquito, Anopheles gambiae s.s. Journal of insect science (Online). 2010; 10(?):57. doi: 10.1673/031.010.5701. [PMID: 20569134]
  • Fong-Chin Huang, Péter Molnár, Wilfried Schwab. Cloning and functional characterization of carotenoid cleavage dioxygenase 4 genes. Journal of experimental botany. 2009; 60(11):3011-22. doi: 10.1093/jxb/erp137. [PMID: 19436048]
  • Sandrine Mathieu, Valeriano Dal Cin, Zhangjun Fei, Hua Li, Peter Bliss, Mark G Taylor, Harry J Klee, Denise M Tieman. Flavour compounds in tomato fruits: identification of loci and potential pathways affecting volatile composition. Journal of experimental botany. 2009; 60(1):325-37. doi: 10.1093/jxb/ern294. [PMID: 19088332]
  • Mwafaq Ibdah, Yaniv Azulay, Vitaly Portnoy, Boris Wasserman, Einat Bar, Ayala Meir, Yossi Burger, Joseph Hirschberg, Arthur A Schaffer, Nurit Katzir, Yaakov Tadmor, Efraim Lewinsohn. Functional characterization of CmCCD1, a carotenoid cleavage dioxygenase from melon. Phytochemistry. 2006 Aug; 67(15):1579-89. doi: 10.1016/j.phytochem.2006.02.009. [PMID: 16563447]
  • Andrew J Simkin, Steven H Schwartz, Michele Auldridge, Mark G Taylor, Harry J Klee. The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles beta-ionone, pseudoionone, and geranylacetone. The Plant journal : for cell and molecular biology. 2004 Dec; 40(6):882-92. doi: 10.1111/j.1365-313x.2004.02263.x. [PMID: 15584954]