FAL 8:1 (BioDeep_00000629903)

 

Secondary id: BioDeep_00000013870, BioDeep_00000227811, BioDeep_00000860545, BioDeep_00001868137


代谢物信息卡片


(2E)-2-Octenal

化学式: C8H14O (126.10445940000001)
中文名称: E-2-辛烯醛, 2-辛烯醛
谱图信息: 最多检出来源 Viridiplantae(plant) 0.06%

分子结构信息

SMILES: C/C=C/CCCCC([H])=O
InChI: InChI=1S/C8H14O/c1-2-3-4-5-6-7-8-9/h6-8H,2-5H2,1H3/b7-6+

描述信息

同义名列表

8 个代谢物同义名

6-octenal; FAL 8:1; 5-octenal; 4-octenal; 3-octenal; (2E)-2-Octenal; 2-octen-1-al; 2-octenal



数据库引用编号

28 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(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)

11 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

  • Yi Hong, Qingxia Zheng, Lingtong Cheng, Pingping Liu, Guoyun Xu, Hui Zhang, Peijian Cao, Huina Zhou. Identification and characterization of TMV-induced volatile signals in Nicotiana benthamiana: evidence for JA/ET defense pathway priming in congeneric neighbors via airborne (E)-2-octenal. Functional & integrative genomics. 2023 Aug; 23(3):272. doi: 10.1007/s10142-023-01203-z. [PMID: 37568053]
  • Jianwei Chen, Yaojia Lu, Xinyi Ye, Mahmoud Emam, Huawei Zhang, Hong Wang. Current advances in Vibrio harveyi quorum sensing as drug discovery targets. European journal of medicinal chemistry. 2020 Dec; 207(?):112741. doi: 10.1016/j.ejmech.2020.112741. [PMID: 32871343]
  • Orna Liarzi, Marina Benichis, Abraham Gamliel, David Ezra. trans-2-Octenal, a single compound of a fungal origin, controls Sclerotium rolfsii, both in vitro and in soil. Pest management science. 2020 Jun; 76(6):2068-2071. doi: 10.1002/ps.5744. [PMID: 31943663]
  • Martina Havlikova, Tereza Bosakova, Georg Petschenka, Radomir Cabala, Alice Exnerova, Zuzana Bosakova. Analysis of defensive secretion of a milkweed bug Lygaeus equestris by 1D GC-MS and GC×GC-MS: sex differences and host-plant effect. Scientific reports. 2020 02; 10(1):3092. doi: 10.1038/s41598-020-60056-9. [PMID: 32080314]
  • Antonio Raffo, Maurizio Masci, Elisabetta Moneta, Stefano Nicoli, José Sánchez Del Pulgar, Flavio Paoletti. Characterization of volatiles and identification of odor-active compounds of rocket leaves. Food chemistry. 2018 Feb; 240(?):1161-1170. doi: 10.1016/j.foodchem.2017.08.009. [PMID: 28946238]
  • John F Anderson, Francis J Ferrandino, Michael P Vasil, Robert H Bedoukian, Marie Maher, Karen Mckenzie. Relatively Small Quantities of CO2, Ammonium Bicarbonate, and a Blend of (E)-2-Hexenal Plus (E)-2-Octenal Attract Bed Bugs (Hemiptera: Cimicidae). Journal of medical entomology. 2017 03; 54(2):362-367. doi: 10.1093/jme/tjw189. [PMID: 28399295]
  • Joelle F Olson, Leonard M Ver Vers, Roger D Moon, Stephen A Kells. Two compounds in bed bug feces are sufficient to elicit off-host aggregation by bed bugs, Cimex lectularius. Pest management science. 2017 Jan; 73(1):198-205. doi: 10.1002/ps.4286. [PMID: 27060680]
  • Francisco J Hidalgo, Rosario Zamora. 2-Alkenal-scavenging ability of m-diphenols. Food chemistry. 2014 Oct; 160(?):118-26. doi: 10.1016/j.foodchem.2014.03.071. [PMID: 24799217]
  • Tolgahan Kocadağlı, Neslihan Göncüoğlu, Aytül Hamzalıoğlu, Vural Gökmen. In depth study of acrylamide formation in coffee during roasting: role of sucrose decomposition and lipid oxidation. Food & function. 2012 Sep; 3(9):970-5. doi: 10.1039/c2fo30038a. [PMID: 22796869]
  • Hiroshi M Ueno, Makoto Shiota, Noriko Ueda, Tomoyuki Isogai, Toshiya Kobayashi. Iron-lactoferrin complex reduces iron-catalyzed off-flavor formation in powdered milk with added fish oil. Journal of food science. 2012 Aug; 77(8):C853-8. doi: 10.1111/j.1750-3841.2012.02809.x. [PMID: 22860577]
  • Pierluigi Caboni, Nikoletta G Ntalli, Nadhem Aissani, Ivana Cavoski, Alberto Angioni. Nematicidal activity of (E,E)-2,4-decadienal and (E)-2-decenal from Ailanthus altissima against Meloidogyne javanica. Journal of agricultural and food chemistry. 2012 Feb; 60(4):1146-51. doi: 10.1021/jf2044586. [PMID: 22224661]
  • Taiko Miyasaki, Makiko Hamaguchi, Shiho Yokoyama. Change of volatile compounds in fresh fish meat during ice storage. Journal of food science. 2011 Nov; 76(9):C1319-25. doi: 10.1111/j.1750-3841.2011.02388.x. [PMID: 22416694]
  • Arati A Inamdar, Prakash Masurekar, Joan Wennstrom Bennett. Neurotoxicity of fungal volatile organic compounds in Drosophila melanogaster. Toxicological sciences : an official journal of the Society of Toxicology. 2010 Oct; 117(2):418-26. doi: 10.1093/toxsci/kfq222. [PMID: 20643751]
  • Vincent Harraca, Camilla Ryne, Rickard Ignell. Nymphs of the common bed bug (Cimex lectularius) produce anti-aphrodisiac defence against conspecific males. BMC biology. 2010 Sep; 8(?):121. doi: 10.1186/1741-7007-8-121. [PMID: 20828381]
  • R A Dick, M K Kwak, T R Sutter, T W Kensler. Antioxidative function and substrate specificity of NAD(P)H-dependent alkenal/one oxidoreductase. A new role for leukotriene B4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase. The Journal of biological chemistry. 2001 Nov; 276(44):40803-10. doi: 10.1074/jbc.m105487200. [PMID: 11524419]
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  • M Alaiz, S Barragán. Changes induced in bovine serum albumin following interactions with the lipid peroxidation product E-2-octenal. Chemistry and physics of lipids. 1995 Aug; 77(2):217-23. doi: 10.1016/0009-3084(95)02470-4. [PMID: 7586100]
  • M Alaiz, M Beppu, K Ohishi, K Kikugawa. Modification of delipidated apoprotein B of low density lipoprotein by lipid oxidation products in relation to macrophage scavenger receptor binding. Biological & pharmaceutical bulletin. 1994 Jan; 17(1):51-7. doi: 10.1248/bpb.17.51. [PMID: 8148817]
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  • K Hasegawa, K Fujimoto, T Kaneda, E N Frankel. Characterization of fluorescent products from reaction of methyl linoleate hydroperoxides with adenine in the presence of Fe2+ and ascorbic acid. Biochimica et biophysica acta. 1988 Oct; 962(3):371-6. doi: 10.1016/0005-2760(88)90267-6. [PMID: 3167087]
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