(R)-(E)-4,7-Megastigmadien-9-one (BioDeep_00000019578)

Main id: BioDeep_00000009222

Secondary id: BioDeep_00000620009

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


3-Buten-2-one, 4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (R)-(+)- (8ci)

化学式: C13H20O (192.1514)
中文名称: α-紫罗酮
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=O)/C=C/[C@H]1C(C)=CCCC1(C)C
InChI: InChI=1S/C13H20O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h6-8,12H,5,9H2,1-4H3/b8-7+/t12-/m0/s1

描述信息

(R)-(E)-4,7-Megastigmadien-9-one is a constituent of many essential oils. (R)-(E)-4,7-Megastigmadien-9-one is a flavouring agent with woody-violet fragrance
Constituent of many essential oils. Flavouring agent with woody-violet fragrance

同义名列表

16 个代谢物同义名

3-Buten-2-one, 4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (R)-(+)- (8ci); (3E)-4-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]but-3-en-2-one; 4-[(1R)-2,6,6-Trimethyl-2-cyclohexen-1-yl]-(3E)-3-buten-2-one; [R-(E)]-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one; (R-(e))-4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-buten-2-one; (R)-(E)-4,7-Megastigmadien-9-one; (+)-(6R)-alpha-Ionone; (R)-(+)-alpha-Ionone; (+)-alpha-Ionone; (R)-alpha-Ionone; .alpha.-Ionone; alpha-Ionone; α-ionone; Parmone; alpha-Ionone; alpha-Ionone



数据库引用编号

14 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)

2 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

  • S Saeidnia, Ar Gohari, N Mokhber-Dezfuli, F Kiuchi. A review on phytochemistry and medicinal properties of the genus Achillea. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences. 2011; 19(3):173-86. doi: ". [PMID: 22615655]
  • Susanne Baldermann, Masaya Kato, Miwako Kurosawa, Yoshiko Kurobayashi, Akira Fujita, Peter Fleischmann, Naoharu Watanabe. Functional characterization of a carotenoid cleavage dioxygenase 1 and its relation to the carotenoid accumulation and volatile emission during the floral development of Osmanthus fragrans Lour. Journal of experimental botany. 2010 Jun; 61(11):2967-77. doi: 10.1093/jxb/erq123. [PMID: 20478967]
  • Ufuk Ozgen, Handan Sevindik, Cavit Kazaz, Demet Yigit, Ali Kandemir, Hasan Secen, Ihsan Calis. A new sulfated alpha-ionone glycoside from Sonchus erzincanicus Matthews. Molecules (Basel, Switzerland). 2010 Apr; 15(4):2593-9. doi: 10.3390/molecules15042593. [PMID: 20428066]
  • Tatsuaki Ishida, Hiroshi Enomoto, Ritsuo Nishida. New attractants for males of the solanaceous fruit fly Bactrocera latifrons. Journal of chemical ecology. 2008 Dec; 34(12):1532-5. doi: 10.1007/s10886-008-9562-8. [PMID: 19018595]
  • Sarah M M Malowicki, Robert Martin, Michael C Qian. Comparison of sugar, acids, and volatile composition in raspberry bushy dwarf virus-resistant transgenic raspberries and the wild type 'meeker' (rubus idaeus L.). Journal of agricultural and food chemistry. 2008 Aug; 56(15):6648-55. doi: 10.1021/jf800253e. [PMID: 18598047]
  • Jules Beekwilder, Ingrid M van der Meer, Ana Simic, Jan Uitdewilligen, Jeroen van Arkel, Ric C H de Vos, Harry Jonker, Francel W A Verstappen, Harro J Bouwmeester, Ole Sibbesen, Ingmar Qvist, Jørn D Mikkelsen, Robert D Hall. Metabolism of carotenoids and apocarotenoids during ripening of raspberry fruit. BioFactors (Oxford, England). 2008; 34(1):57-66. doi: ". [PMID: 19706972]
  • Hajime Shimomura, Hideo Etoh, Masaharu Mizutani, Nobuhiro Hirai, Yasushi Todoroki. Effect of the minor ABA metabolite 7'-hydroxy-ABA on Arabidopsis ABA 8'-hydroxylase CYP707A3. Bioorganic & medicinal chemistry letters. 2007 Sep; 17(17):4977-81. doi: 10.1016/j.bmcl.2007.06.018. [PMID: 17582765]
  • María del Mar Caja, Christina Preston, Michael Kempf, Peter Schreier. Flavor authentication studies of alpha-ionone, beta-ionone, and alpha-ionol from various sources. Journal of agricultural and food chemistry. 2007 Aug; 55(16):6700-4. doi: 10.1021/jf070805r. [PMID: 17630763]
  • 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]
  • Ming Wei, Xiaojun Deng, Jiawei Du. [Analysis and identification of Liriomyza sativae-attractants from cowpea and kidney bean volatiles]. Ying yong sheng tai xue bao = The journal of applied ecology. 2005 May; 16(5):907-10. doi: . [PMID: 16110669]
  • Grant T McQuate, Young Soo Keum, Charmaine D Sylva, Qing X Li, Eric B Jang. Active ingredients in cade oil that synergize attractiveness of alpha-ionol to male Bactrocera latifrons (Diptera: Tephritidae). Journal of economic entomology. 2004 Jun; 97(3):862-70. doi: 10.1603/0022-0493(2004)097[0862:aiicot]2.0.co;2. [PMID: 15279265]
  • T Murakami, K Kohno, K Ninomiya, H Matsuda, M Yoshikawa. Medicinal foodstuffs. XXV. Hepatoprotective principle and structures of ionone glucoside, phenethyl glycoside, and flavonol oligoglycosides from young seedpods of garden peas, Pisum sativum L. Chemical & pharmaceutical bulletin. 2001 Aug; 49(8):1003-8. doi: 10.1248/cpb.49.1003. [PMID: 11515568]
  • G T McQuate, S L Peck. Enhancement of attraction of alpha-ionol to male Bactrocera latifrons (Diptera: Tephritidae) by addition of a synergist, cade oil. Journal of economic entomology. 2001 Feb; 94(1):39-46. doi: 10.1603/0022-0493-94.1.39. [PMID: 11233131]
  • N Vogt, A Englhardt. [Different forms of hyperlipoproteinemia in diabetics (author's transl)]. Medizinische Klinik. 1975 Nov; 70(46):1871-7. doi: NULL. [PMID: 171548]