(R)-3,7-Dimethyl-1,6-octadien-3-ol (BioDeep_00000014735)

 

Secondary id: BioDeep_00000016652, BioDeep_00000620234, BioDeep_00000872643, BioDeep_00001891228

human metabolite PANOMIX_OTCML-2023 Endogenous Volatile Flavor Compounds


代谢物信息卡片


(R)-(-)-3,7-Dimethyl-1,6-octadien-3-ol

化学式: C10H18O (154.1357578)
中文名称: (S)-3,7-二甲基-1,6-辛二烯-3-醇, L-芳樟醇
谱图信息: 最多检出来源 Homo sapiens(feces) 0.47%

分子结构信息

SMILES: C(=CCC[C@@](C=C)(O)C)(C)C
InChI: InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m1/s1

描述信息

(R)-3,7-Dimethyl-1,6-octadien-3-ol is found in coriander. (R)-3,7-Dimethyl-1,6-octadien-3-ol is a constituent of many essential oils including Melissa officinalis (lemon balm), rose, neroli and lavender. (R)-3,7-Dimethyl-1,6-octadien-3-ol is a major component of oil of field mint (Mentha arvensis)
Constituent of many essential oils including Melissa officinalis (lemon balm), rose, neroli and lavender. Major component of oil of field mint (Mentha arvensis). L-Linalool is found in many foods, some of which are tea, cumin, pummelo, and coriander.

同义名列表

28 个代谢物同义名

(R)-(-)-3,7-Dimethyl-1,6-octadien-3-ol; (3S)-3,7-dimethylocta-1,6-dien-3-ol; (3R)-3,7-Dimethyl-1,6-octadien-3-ol; (3S)-3,7-Dimethyl-1,6-octadien-3-ol; (3R)-3,7-Dimethylocta-1,6-dien-3-ol; (R)-3,7-Dimethyl-1,6-octadien-3-ol; (-)-3,7-Dimethyl-1,6-octadien-3-ol; (S)-3,7-Dimethyl-1,6-octadien-3-ol; (R)-(-)-Linalool; (S)-(+)-Linalool; dextro-linalool; S-(+)-Linalool; Linalool, (+)-; (-)-R-Linalool; (+)-S-Linalool; (3S)-Linalool; (3R)-Linalool; (R)-linalool; (+)-Linalool; (S)-Linalool; (-)-Linalool; (S)-Linalol; (R)-Linalol; Coriandrol; L-Linalool; Licareol; (-)-Linalool; (+)-Linalool



数据库引用编号

19 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

18 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(9)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(8)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

55 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

  • Y Xiao, Q Wang, M Erb, T C J Turlings, L Ge, L Hu, J Li, X Han, T Zhang, J Lu, G Zhang, Y Lou. Specific herbivore-induced volatiles defend plants and determine insect community composition in the field. Ecology letters. 2012 Oct; 15(10):1130-9. doi: 10.1111/j.1461-0248.2012.01835.x. [PMID: 22804824]
  • Bing-Ho Cheng, Chun-Ya Lin, Ting-Feng Yeh, Sen-Sung Cheng, Shang-Tzen Chang. Potential source of S-(+)-linalool from Cinnamomum osmophloeum ct. linalool leaf: essential oil profile and enantiomeric purity. Journal of agricultural and food chemistry. 2012 Aug; 60(31):7623-8. doi: 10.1021/jf302248w. [PMID: 22769589]
  • Juri Battilana, Francesco Emanuelli, Giorgio Gambino, Ivana Gribaudo, Flavia Gasperi, Paul K Boss, Maria Stella Grando. Functional effect of grapevine 1-deoxy-D-xylulose 5-phosphate synthase substitution K284N on Muscat flavour formation. Journal of experimental botany. 2011 Nov; 62(15):5497-508. doi: 10.1093/jxb/err231. [PMID: 21868399]
  • Emily J McCallum, John Paul Cunningham, Joost Lücker, Myron P Zalucki, James J De Voss, José R Botella. Increased plant volatile production affects oviposition, but not larval development, in the moth Helicoverpa armigera. The Journal of experimental biology. 2011 Nov; 214(Pt 21):3672-7. doi: 10.1242/jeb.059923. [PMID: 21993797]
  • Teun Dekker, Rickard Ignell, Maedot Ghebru, Robert Glinwood, Richard Hopkins. Identification of mosquito repellent odours from Ocimum forskolei. Parasites & vectors. 2011 Sep; 4(?):183. doi: 10.1186/1756-3305-4-183. [PMID: 21936953]
  • A J Matich, D J Comeskey, B J Bunn, M B Hunt, D D Rowan. Biosynthesis and enantioselectivity in the production of the lilac compounds in Actinidia arguta flowers. Phytochemistry. 2011 May; 72(7):579-86. doi: 10.1016/j.phytochem.2011.01.035. [PMID: 21377706]
  • Danilo C Centeno, Sonia Osorio, Adriano Nunes-Nesi, Ana L F Bertolo, Raphael T Carneiro, Wagner L Araújo, Marie-Caroline Steinhauser, Justyna Michalska, Johannes Rohrmann, Peter Geigenberger, Sandra N Oliver, Mark Stitt, Fernando Carrari, Jocelyn K C Rose, Alisdair R Fernie. Malate plays a crucial role in starch metabolism, ripening, and soluble solid content of tomato fruit and affects postharvest softening. The Plant cell. 2011 Jan; 23(1):162-84. doi: 10.1105/tpc.109.072231. [PMID: 21239646]
  • Carolina E Reisenman, Jeffrey A Riffell, Elizabeth A Bernays, John G Hildebrand. Antagonistic effects of floral scent in an insect-plant interaction. Proceedings. Biological sciences. 2010 Aug; 277(1692):2371-9. doi: 10.1098/rspb.2010.0163. [PMID: 20335210]
  • Adam J Matich, Barry J Bunn, Martin B Hunt. The enantiomeric composition of linalool and linalool oxide in the flowers of kiwifruit (Actinidia) species. Chirality. 2010 Jan; 22(1):110-9. doi: 10.1002/chir.20713. [PMID: 19382237]
  • Xiaofeng Zhuang, William E Klingeman, Jun Hu, Feng Chen. Emission of volatile chemicals from flowering dogwood (cornus Florida L.) flowers. Journal of agricultural and food chemistry. 2008 Oct; 56(20):9570-4. doi: 10.1021/jf801651v. [PMID: 18811168]
  • Joshua S Yuan, Tobias G Köllner, Greg Wiggins, Jerome Grant, Nan Zhao, Xiaofeng Zhuang, Jörg Degenhardt, Feng Chen. Elucidation of the genomic basis of indirect plant defense against insects. Plant signaling & behavior. 2008 Sep; 3(9):720-1. doi: 10.4161/psb.3.9.6468. [PMID: 19704839]
  • Joshua S Yuan, Tobias G Köllner, Greg Wiggins, Jerome Grant, Jörg Degenhardt, Feng Chen. Molecular and genomic basis of volatile-mediated indirect defense against insects in rice. The Plant journal : for cell and molecular biology. 2008 Aug; 55(3):491-503. doi: 10.1111/j.1365-313x.2008.03524.x. [PMID: 18433439]
  • Tomoko Okamoto, Atsushi Kawakita, Makoto Kato. Interspecific variation of floral scent composition in Glochidion and its association with host-specific pollinating seed parasite (Epicephala). Journal of chemical ecology. 2007 May; 33(5):1065-81. doi: 10.1007/s10886-007-9287-0. [PMID: 17394049]
  • Stig Ulland, E Ian, A-K Borg-Karlson, H Mustaparta. Discrimination between enantiomers of linalool by olfactory receptor neurons in the cabbage moth Mamestra brassicae (L.). Chemical senses. 2006 May; 31(4):325-34. doi: 10.1093/chemse/bjj036. [PMID: 16495438]
  • Daniela Hampel, Armin Mosandl, Matthias Wüst. Biosynthesis of mono- and sesquiterpenes in strawberry fruits and foliage: 2H labeling studies. Journal of agricultural and food chemistry. 2006 Feb; 54(4):1473-8. doi: 10.1021/jf0523972. [PMID: 16478276]
  • Kyoko Kuroda, Naohiko Inoue, Yuriko Ito, Kikue Kubota, Akio Sugimoto, Takami Kakuda, Tohru Fushiki. Sedative effects of the jasmine tea odor and (R)-(-)-linalool, one of its major odor components, on autonomic nerve activity and mood states. European journal of applied physiology. 2005 Oct; 95(2-3):107-14. doi: 10.1007/s00421-005-1402-8. [PMID: 15976995]
  • T Røstelien, M Stranden, A-K Borg-Karlson, H Mustaparta. Olfactory receptor neurons in two Heliothine moth species responding selectively to aliphatic green leaf volatiles, aromatic compounds, monoterpenes and sesquiterpenes of plant origin. Chemical senses. 2005 Jun; 30(5):443-61. doi: 10.1093/chemse/bji039. [PMID: 15917371]
  • Antonio C Siani, Marcelo R R Tappin, Mônica F S Ramos, José L Mazzei, Maria Conceição K V Ramos, Francisco R De Aquino Neto, Nélson Frighetto. Linalool from Lippia alba: study of the reproducibility of the essential oil profile and the enantiomeric purity. Journal of agricultural and food chemistry. 2002 Jun; 50(12):3518-21. doi: 10.1021/jf011592n. [PMID: 12033821]
  • E Lewinsohn, F Schalechet, J Wilkinson, K Matsui, Y Tadmor, K H Nam, O Amar, E Lastochkin, O Larkov, U Ravid, W Hiatt, S Gepstein, E Pichersky. Enhanced levels of the aroma and flavor compound S-linalool by metabolic engineering of the terpenoid pathway in tomato fruits. Plant physiology. 2001 Nov; 127(3):1256-65. doi: . [PMID: 11706204]
  • J Lücker, H J Bouwmeester, W Schwab, J Blaas, L H van der Plas, H A Verhoeven. Expression of Clarkia S-linalool synthase in transgenic petunia plants results in the accumulation of S-linalyl-beta-D-glucopyranoside. The Plant journal : for cell and molecular biology. 2001 Aug; 27(4):315-24. doi: 10.1046/j.1365-313x.2001.01097.x. [PMID: 11532177]