3,7-Dimethyl-1,6-octadien-3-ol (BioDeep_00000000443)

 

Secondary id: BioDeep_00000016652

human metabolite PANOMIX_OTCML-2023 Endogenous Antitumor activity Volatile Flavor Compounds


代谢物信息卡片


Linalool, certified reference material, TraceCERT(R)

化学式: C10H18O (154.1357578)
中文名称: 芳樟醇
谱图信息: 最多检出来源 Homo sapiens(feces) 0.15%

分子结构信息

SMILES: C=CC(C)(O)CCC=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

描述信息

3,7-Dimethyl-1,6-octadien-3-ol, also known simply as linalool is a naturally occurring terpene alcohol. It belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. Linalool has a role as a plant metabolite, a volatile oil component, an antimicrobial agent and a fragrance. There are two stereoisomers of Linalool – (S)-linalool and (R)-linalool. Linalool is used as a scent in 60\\\\\% to 80\\\\\% of perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions. Linalool is also used by pest professionals as a flea, fruit fly, and cockroach insecticide. Linalool is found in more than 200 different species of plants, including many flowers and spice plants. (S)-linalool is found, for example, as a major constituent of the essential oils of coriander (Coriandrum sativum L.), cymbopogon (Cymbopogon martini var. martinii), and sweet orange (Citrus sinensis) flowers. (R)-linalool is present in lavender (Lavandula officinalis), bay laurel (Laurus nobilis), and sweet basil (Ocimum basilicum), among others. Linalool is also found in plants from the Lamiaceae family (mint and other herbs), Lauraceae (laurels, cinnamon, rosewood), Cinnamomum tamala, Solidago Meyen, Artemisia vulgaris (mugwort), Humulus lupulus. Linalool is also one of several monoterpenes that are found in cannabis plants (PMID:6991645 ). There are more than 140 known terpenes in cannabis and the combination of these terepenoids produces the skunky, fruity odor characteristic of C. savita. Like the majority of monoterpenes, linalool starts with the condensation of dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP) to form geranyl pyrophosphate (GPP) (PMID:7640522 ). Linalool is then synthesized with the aid of linalool synthase (LIS) (PMID:12572612 ). Linalool has a citrus, floral, rose, woody aroma and a citrus, orange, waxy taste. Linalool is found in a few different foods and spices, such as spearmints, corianders, common thymes, limes, grapes, lemons, grapefruit, oranges, pineapples, blackcurrants, basil, and common oregano. This could make, Linalool a potential biomarker for the consumption of these foods. Linalool is also synthesized, de novo, by yeast (C. cerevisiae) and may contribute to the floral tones found in some wines (PMID:15668008 ).
Linalool is a monoterpenoid that is octa-1,6-diene substituted by methyl groups at positions 3 and 7 and a hydroxy group at position 3. It has been isolated from plants like Ocimum canum. It has a role as a plant metabolite, a volatile oil component, an antimicrobial agent and a fragrance. It is a tertiary alcohol and a monoterpenoid.
Linalool is a natural product found in Nepeta nepetella, Teucrium montanum, and other organisms with data available.
3,7-Dimethyl-1,6-octadien-3-ol is a metabolite found in or produced by Saccharomyces cerevisiae.
See also: Cinnamon Leaf Oil (part of); Clary Sage Oil (part of); Cannabis sativa subsp. indica top (part of) ... View More ...
A monoterpenoid that is octa-1,6-diene substituted by methyl groups at positions 3 and 7 and a hydroxy group at position 3. It has been isolated from plants like Ocimum canum.
Flavouring agent. Widespread natural occurrence as the optically active and racemic forms in over 200 essential oilsand is) also present in numerous fruits.
D010575 - Pesticides > D007306 - Insecticides
D016573 - Agrochemicals
Linalool is natural monoterpene in essential olis of coriander, acts as a competitive antagonist of Nmethyl d-aspartate (NMDA) receptor, with anti-tumor, anti-cardiotoxicity activity[1].Linalool is a PPARα ligand that reduces plasma TG levels and rewires the hepatic transcriptome and plasma metabolome[2].
Linalool is a natural monoterpene which is a competitive NMDA receptor antagonist. Linalool is orally active and crosses the blood-brain barrier. Linalool has anticancer, antibacterial, anti-inflammatory, neuroprotective, anxiolytic, antidepressant, anti-stress, cardioprotective, hepatoprotective, nephroprotective and pulmonary protective activities[1][2][3][4][5].
Linalool is natural monoterpene in essential olis of coriander, acts as a competitive antagonist of Nmethyl d-aspartate (NMDA) receptor, with anti-tumor, anti-cardiotoxicity activity[1].Linalool is a PPARα ligand that reduces plasma TG levels and rewires the hepatic transcriptome and plasma metabolome[2].

同义名列表

81 个代谢物同义名

Linalool, certified reference material, TraceCERT(R); Linalool, primary pharmaceutical reference standard; 0-01-00-00462 (Beilstein Handbook Reference); dl-3,7-Dimethyl-3-hydroxy-1,6-octadiene; (R)-(-)-3,7-Dimethyl-1,6-octadien-3-ol; 7-methyl-3-methyleneocta-4,6-dien-2-ol; ( inverted exclamation markA)-Linalool; (1)-3,7-Dimethyl-1,6-octadien-3-ol; 2,7-Octadien-6-ol, 2,6-dimethyl-; 1,6-Octadien-3-ol, 3,7-dimethyl-; 2,6-Dimethyl-2,7-octadiene-6-ol; 3,7-dimethyl-octa-1,6-dien-3-ol; 3,7-Dimethyl-1, 6-octadien-3-ol; 2,6-Dimethylocta-2,7-dien-6-ol; 3,7-dimethyl-1,6-octadien-3-ol; 2,6-Dimethyl-2,7-octadien-6-ol; 3,7-Dimethylocta-1,6-dien-3-ol; Linalool, analytical standard; linalool, titanium (4+) salt; Linalool, >=97\\%, FCC, FG; 1, 3,7-dimethyl-, (-)-; WLN: 1Y1&U3XQ1&1U1 -,-; linalool, (+-)-isomer; linalool, (S)-isomer; linalool, (R)-isomer; WLN: 1U1XQ1&3UY1&1; Linalool (natural); 2,7-octadiene-6-ol; 3,6-octadien-3-ol; LINALOOL (USP-RS); LINALOOL [WHO-DD]; LINALOOL [USP-RS]; Linalool, (+/-)-; (.+/-.)-Linalool; Linalool, .beta.; LINALOOL [FHFI]; LINALOOL [INCI]; UNII-D81QY6I88E; linalool, (+-)-; LINALOOL [HSDB]; LINALYL ALCOHOL; .beta.-Linalool; LINALOOL [FCC]; Linalool, 97\\%; (+/-)-linalool; beta-Linalool; (+-)-Linalool; allo-ocimenol; 3,6-dien-3-ol; LINALOOL, DL-; LINALOOL [MI]; 2,7-dien-6-ol; (RS)-Linalool; Tox21_303037; (R)-linalool; Tox21_201658; LINALOOL OIL; ( )-linalool; LINOLOOL (D); Linalool,(S); (S)-Linalol; |A-Linalool; CAS-78-70-6; dl-Linalool; Β-linalool; D81QY6I88E; p-Linalool; b-Linalool; Linalool b; DIABEXALL; AI3-00942; FEMA 2635; linalool; Linolool; Linanool; Licareol; Phantol; Linalol; muguol; Linalool; Linalool



数据库引用编号

24 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(2)

BioCyc(0)

PlantCyc(0)

代谢反应

3 个相关的代谢反应过程信息。

Reactome(2)

  • Olfactory Signaling Pathway: GTP + odorant:Olfactory Receptor:GNAL:GDP:GNB1:GNG13 ⟶ GDP + odorant:Olfactory Receptor:GNAL:GTP:GNB1:GNG13
  • Sensory Perception: GTP + odorant:Olfactory Receptor:GNAL:GDP:GNB1:GNG13 ⟶ GDP + odorant:Olfactory Receptor:GNAL:GTP:GNB1:GNG13

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

565 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

  • Qiwei Wang, Jialing Xie, Lilei Wang, Yongwen Jiang, Yuliang Deng, Jiayi Zhu, Haibo Yuan, Yanqin Yang. Comprehensive investigation on the dynamic changes of volatile metabolites in fresh scent green tea during processing by GC-E-Nose, GC-MS, and GC × GC-TOFMS. Food research international (Ottawa, Ont.). 2024 Jul; 187(?):114330. doi: 10.1016/j.foodres.2024.114330. [PMID: 38763633]
  • Xueying Song, Xingyan Wei, Liu Liu, Yongfeng Liu. Gelatin/agar pH-indicator film based on cranberry extract loaded with linalool nanoparticle: Survey on physical, antimicrobial, and antioxidant properties. International journal of biological macromolecules. 2024 May; 268(Pt 2):131767. doi: 10.1016/j.ijbiomac.2024.131767. [PMID: 38657918]
  • Felipe Nardo Dos Santos, Laura Martins Fonseca, Cristina Jansen-Alves, Rosane Lopes Crizel, Juliani Buchveitz Pires, Isabela Schneid Kroning, Jaqueline Ferreira de Souza, André Ricardo Fajardo, Graciela Völz Lopes, Alvaro Renato Guerra Dias, Elessandra da Rosa Zavareze. Antimicrobial activity of geranium (Pelargonium graveolens) essential oil and its encapsulation in carioca bean starch ultrafine fibers by electrospinning. International journal of biological macromolecules. 2024 Apr; 265(Pt 1):130953. doi: 10.1016/j.ijbiomac.2024.130953. [PMID: 38499124]
  • Zohreh Jahanafrooz, Mir Mohammad Hossein Mousavi, Soghra Akbarzadeh, Maedeh Hemmatzadeh, Filippo Maggi, Mohammad Reza Morshedloo. Anti-breast cancer activity of the essential oil from grapefruit mint (Mentha suaveolens × piperita). Fitoterapia. 2024 Apr; 174(?):105875. doi: 10.1016/j.fitote.2024.105875. [PMID: 38417678]
  • Kenan Preljević, Ivana Pašić, Milorad Vlaović, Ivana Z Matić, Slađana Krivokapić, Nina Petrović, Tatjana Stanojković, Vladimir Živković, Svetlana Perović. Comparative analysis of chemical profiles, antioxidant, antibacterial, and anticancer effects of essential oils of two Thymus species from Montenegro. Fitoterapia. 2024 Apr; 174(?):105871. doi: 10.1016/j.fitote.2024.105871. [PMID: 38428618]
  • Guanhua Liu, Qian Wang, Hui Chen, Yuxi Wang, Xiaogui Zhou, Demeng Bao, Nuo Wang, Juan Sun, Fuyin Huang, Mei Yang, Han Zhang, Peng Yan, Xin Li, Jiang Shi, Jianyu Fu. Plant-derived monoterpene S-linalool and β-ocimene generated by CsLIS and CsOCS-SCZ are key chemical cues for attracting parasitoid wasps for suppressing Ectropis obliqua infestation in Camellia sinensis L. Plant, cell & environment. 2024 Mar; 47(3):913-927. doi: 10.1111/pce.14803. [PMID: 38168880]
  • Xuping Liu, Wenxin Yan, Sijia Liu, Jing Wu, Pingsheng Leng, Zenghui Hu. LiNAC100 contributes to linalool biosynthesis by directly regulating LiLiS in Lilium 'Siberia'. Planta. 2024 Feb; 259(4):73. doi: 10.1007/s00425-024-04340-2. [PMID: 38393405]
  • Yinliang Wang, Huanhuan Dong, Yafei Qu, Yuxin Zhou, Jianhui Qin, Kebin Li, Chen Luo, Bingzhong Ren, Yazhong Cao, Shuai Zhang, Jiao Yin, Walter S Leal. Circabidian rhythm of sex pheromone reception in a scarab beetle. Current biology : CB. 2024 02; 34(3):568-578.e5. doi: 10.1016/j.cub.2023.12.057. [PMID: 38242123]
  • Jessica P Yactayo-Chang, Geoffrey T Broadhead, Robert J Housler, Marcio F R Resende, Kashish Verma, Joe Louis, Gilles J Basset, John J Beck, Anna K Block. Maize terpene synthase 1 impacts insect behavior via the production of monoterpene volatiles β-myrcene and linalool. Phytochemistry. 2024 Feb; 218(?):113957. doi: 10.1016/j.phytochem.2023.113957. [PMID: 38154731]
  • Elisa Schuh, Sina Cassau, Ahmed R Ismaieel, Regina Stieber, Jürgen Krieger, Bill S Hansson, Silke Sachse, Sonja Bisch-Knaden. Females smell differently: characteristics and significance of the most common olfactory sensilla of female silkmoths. Proceedings. Biological sciences. 2024 Jan; 291(2015):20232578. doi: 10.1098/rspb.2023.2578. [PMID: 38228178]
  • Giulia Coradello, Chiara Setti, Roberto Donno, Matilde Ghibaudi, Federico Catalano, Nicola Tirelli. A Quantitative Re-Assessment of Microencapsulation in (Pre-Treated) Yeast. Molecules (Basel, Switzerland). 2024 Jan; 29(2):. doi: 10.3390/molecules29020539. [PMID: 38276617]
  • Cancan Song, Die Chen, Chunxian Jiang, Chengcheng Li, Lin Chen, Rong Huang, Xian Wang, Jie Qin, Qing Li. Herbivore-induced plant volatiles emitted by citrus in response to spider mite infestation can attract predatory mites. Journal of economic entomology. 2024 Jan; ?(?):. doi: 10.1093/jee/toae009. [PMID: 38253912]
  • Tianyu Huang, Meng Lai, Zhenwei Lin, Ruiqi Luo, Xuezheng Xiang, Haozhe Xu, Ning Pan, Zhaojiang Zuo. Identification of algicidal monoterpenoids from four chemotypes of Cinnamomum camphora and their algicidal mechanisms on Microcystis aeruginosa. Environmental research. 2024 Jan; 241(?):117714. doi: 10.1016/j.envres.2023.117714. [PMID: 37989462]
  • Ibrahim Taha Radwan, Nirvina Abdel Raouf Ghazawy, Abeer Mousa Alkhaibari, Hattan S Gattan, Mohammed H Alruhaili, Abdelfattah Selim, Mostafa E Salem, Eman Alaaeldin AbdelFattah, Heba M Hamama. Nanostructure Lipid Carrier of Curcumin Co-Delivered with Linalool and Geraniol Monoterpenes as Acetylcholinesterase Inhibitor of Culex pipiens. Molecules (Basel, Switzerland). 2024 Jan; 29(1):. doi: 10.3390/molecules29010271. [PMID: 38202854]
  • XiaoLong Liu, Wang Liao, ZheRan Wu, YiWen Pei, ZhiQiang Wei, Min Lu. Binding Properties of Odorant-Binding Protein 7 to Host Volatiles in Larvae of Spodoptera frugiperda. Journal of agricultural and food chemistry. 2023 Dec; 71(51):20671-20679. doi: 10.1021/acs.jafc.3c06833. [PMID: 38103022]
  • Ziwei Xin, Wenjia Wang, Weizong Yang, Yajie Li, Lixin Niu, Yanlong Zhang. Investigation of Volatile Components and Assessment of Antioxidant Potential in Seven Lamiaceae Plant Hydrosols. Molecules (Basel, Switzerland). 2023 Dec; 29(1):. doi: 10.3390/molecules29010145. [PMID: 38202728]
  • Anna Jakubska-Busse, Izabela Czeluśniak, Marek Hojniak, Monika Myśliwy, Kamil Najberek. Chemical Insect Attractants Produced by Flowers of Impatiens spp. (Balsaminaceae) and List of Floral Visitors. International journal of molecular sciences. 2023 Dec; 24(24):. doi: 10.3390/ijms242417259. [PMID: 38139088]
  • Long Liu, Fan Wang, Wei Yang, Hua Yang, Qiong Huang, Chunlin Yang, Wenkai Hui. Molecular and Functional Characterization of Pheromone Binding Protein 2 from Cyrtotrachelus buqueti (Coleoptera: Curculionidae). International journal of molecular sciences. 2023 Nov; 24(23):. doi: 10.3390/ijms242316925. [PMID: 38069247]
  • Pravesh Bhargav, Seema Chaurasia, Aashish Kumar, Gaurav Srivastava, Yatish Pant, Chandan Singh Chanotiya, Sumit Ghosh. Unraveling the terpene synthase family and characterization of BsTPS2 contributing to (S)-( +)-linalool biosynthesis in Boswellia. Plant molecular biology. 2023 Nov; 113(4-5):219-236. doi: 10.1007/s11103-023-01384-y. [PMID: 37898975]
  • Lars Hareng, Susanne N Kolle, Caroline Gomes, Steffen Schneider, Markus Wahl. Critical assessment of the endocrine potential of Linalool and Linalyl acetate: proactive testing strategy assessing estrogenic and androgenic activity of Lavender oil main components. Archives of toxicology. 2023 Oct; ?(?):. doi: 10.1007/s00204-023-03623-z. [PMID: 37906319]
  • P Tamilmani, V V Sathibabu Uddandrao, P Chandrasekaran, G Saravanan, Parim Brahmanaidu, S Sengottuvelu, S Vadivukkarasi. Linalool attenuates lipid accumulation and oxidative stress in metabolic dysfunction-associated steatotic liver disease via Sirt1/Akt/PPRA-α/AMPK and Nrf-2/HO-1 signaling pathways. Clinics and research in hepatology and gastroenterology. 2023 Oct; ?(?):102231. doi: 10.1016/j.clinre.2023.102231. [PMID: 37865226]
  • Arlene Sobrinho Ventura, Ruy Alberto Caetano Corrêa Filho, Claudia Andrea Lima Cardoso, Giovanna Rodrigues Stringhetta, Lucas de Oliveira Brasileiro, Juliana Silva Ribeiro, Scheila Anelise Pereira, Gabriela Tomas Jerônimo, Jayme Aparecido Povh. Ocimum basilicum essential oil in pacu Piaractus mesopotamicus: anesthetic efficacy, distribution, and depletion in different tissues. Veterinary research communications. 2023 Oct; ?(?):. doi: 10.1007/s11259-023-10225-8. [PMID: 37851315]
  • H Zhang, C Liu, X Lu, G Xia. Evaluation of growth adaptation of Cinnamomum camphora seedlings in ionic rare earth tailings environment. Scientific reports. 2023 Oct; 13(1):16910. doi: 10.1038/s41598-023-44145-z. [PMID: 37805611]
  • Zhengyu Bao, Mingcong Fan, Kanza Hannachi, Tingting Li, Jiajia Zhao, Yan Li, Haifeng Qian, Li Wang. Antifungal activity of star anise extract against Penicillium roqueforti and Aspergillus niger for bread shelf life. Food research international (Ottawa, Ont.). 2023 10; 172(?):113225. doi: 10.1016/j.foodres.2023.113225. [PMID: 37689961]
  • N S Younis, R M Abdelnaby, M E Mohamed. Hepatoprotective effects of linalool against liver ischemia-reperfusion: the role of Nrf2/HO-1/NQO1 and TLR4/RAGE/NFκB pathways. European review for medical and pharmacological sciences. 2023 Oct; 27(20):10094-10111. doi: 10.26355/eurrev_202310_34190. [PMID: 37916380]
  • Yan-Hong Wang, Goutam Mondal, Nicole Stevens, Cécile Bascoul, Russell J Osguthorpe, Ikhlas A Khan, Charles R Yates. Development of a Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) Method for Characterizing Linalool Oral Pharmacokinetics in Humans. Molecules (Basel, Switzerland). 2023 Sep; 28(18):. doi: 10.3390/molecules28186457. [PMID: 37764231]
  • Yeasmin Akter Munni, Raju Dash, Ho Jin Choi, Sarmistha Mitra, Md Abdul Hannan, Kishor Mazumder, Binod Timalsina, Il Soo Moon. Differential Effects of the Processed and Unprocessed Garlic (Allium sativum L.) Ethanol Extracts on Neuritogenesis and Synaptogenesis in Rat Primary Hippocampal Neurons. International journal of molecular sciences. 2023 Aug; 24(17):. doi: 10.3390/ijms241713386. [PMID: 37686193]
  • Qiying Wang, Xiaochun Wang, Linhua Huang, Yujiao Cheng, Li Ren, Huayu Yang, Changyong Zhou, Xuefeng Wang, Jun He. Promoter characterization of a citrus linalool synthase gene mediating interspecific variation in resistance to a bacterial pathogen. BMC plant biology. 2023 Aug; 23(1):405. doi: 10.1186/s12870-023-04413-6. [PMID: 37620808]
  • Takashi A Inoue, Mami Suetake, Narumi Nishidzu, Fumio Yokohari, Kinuko Niihara, Tatsuya Fukuda. Behavioral and Electrophysiological Study on Eight Japanese Papilio Species with Five Hostplant Volatiles and Linalool. Journal of chemical ecology. 2023 Aug; 49(7-8):397-407. doi: 10.1007/s10886-023-01433-2. [PMID: 37378686]
  • Bartłomiej Piasecki, Izabela Korona-Głowniak, Anna Kiełtyka-Dadasiewicz, Agnieszka Ludwiczuk. Composition and Anti-Helicobacter pylori Properties of Essential Oils Obtained from Selected Mentha Cultivars. Molecules (Basel, Switzerland). 2023 Jul; 28(15):. doi: 10.3390/molecules28155690. [PMID: 37570659]
  • Eveleny Tirsa Vaca Meza, Jorge Vasquez-Kool, Noé Ildefonso Costilla Sánchez, Amandio Vieira, Rodney Alexandre Ferreira Rodrigues, Adilson Sartoratto, Angela Del Pilar Flores Granados, Carmen Luisa Marin Tello, Ana Lucia Tasca Gois Ruiz. Chemical composition and anti-proliferative activity of essential oils from some medicinal plants from Cachicadán, Región La Libertad, Perú. Natural product research. 2023 Jul; ?(?):1-6. doi: 10.1080/14786419.2023.2238114. [PMID: 37470420]
  • Xun Wang, Jiajie Wang, Xinyi Zhang, Jia Zhang, Yujunjie Zhou, Fei Wang, Xun Li. Efficient myrcene production using linalool dehydratase isomerase and rational biochemical process in Escherichia coli. Journal of biotechnology. 2023 Jul; 371-372(?):33-40. doi: 10.1016/j.jbiotec.2023.05.008. [PMID: 37285942]
  • Shuang-Gang Duan, Ao Liu, Chao Wang, Rui-Lin Zhang, Jing Lu, Man-Qun Wang. Homeotic Protein Distal-Less Regulates NlObp8 and NlCsp10 to Impact the Recognition of Linalool in the Brown Planthopper Nilaparvata lugens. Journal of agricultural and food chemistry. 2023 Jul; 71(27):10291-10303. doi: 10.1021/acs.jafc.3c02293. [PMID: 37382541]
  • Sándor Koczor, Miklós Tóth. Field attraction of Eurydema ornata (Hemiptera: Pentatomidae) to allyl isothiocyanate. Scientific reports. 2023 Jul; 13(1):11063. doi: 10.1038/s41598-023-37705-w. [PMID: 37422493]
  • Pingping Zhou, Xiuqi Zhou, Doudou Yuan, Xin Fang, Xueqing Pang, Ke Yuan, Aipeng Li, Xiqing Wang. Combining Protein and Organelle Engineering for Linalool Overproduction in Saccharomyces cerevisiae. Journal of agricultural and food chemistry. 2023 Jul; 71(26):10133-10143. doi: 10.1021/acs.jafc.2c08416. [PMID: 37350414]
  • Maria O Taratynova, Ekaterina E Tikhonova, Iuliia M Fedyaeva, Dmitry A Dementev, Tigran V Yuzbashev, Andrey I Solovyev, Sergey P Sineoky, Evgeniya Y Yuzbasheva. Boosting Geranyl Diphosphate Synthesis for Linalool Production in Engineered Yarrowia lipolytica. Applied biochemistry and biotechnology. 2023 Jul; ?(?):. doi: 10.1007/s12010-023-04581-z. [PMID: 37392322]
  • Moritz Winker, Antoine Chauveau, Martin Smieško, Olivier Potterat, Alexander Areesanan, Amy Zimmermann-Klemd, Carsten Gründemann. Immunological evaluation of herbal extracts commonly used for treatment of mental diseases during pregnancy. Scientific reports. 2023 Jun; 13(1):9630. doi: 10.1038/s41598-023-35952-5. [PMID: 37316493]
  • Xiaohua Chen, Shufeng Shang, Fei Yan, Hai Jiang, Guanjie Zhao, Shan Tian, Rui Chen, Dejing Chen, Yafeng Dang. Antioxidant Activities of Essential Oils and Their Major Components in Scavenging Free Radicals, Inhibiting Lipid Oxidation and Reducing Cellular Oxidative Stress. Molecules (Basel, Switzerland). 2023 Jun; 28(11):. doi: 10.3390/molecules28114559. [PMID: 37299039]
  • Qian Zhao, Lina Gu, Yuqing Li, Hui Zhi, Jianrang Luo, Yanlong Zhang. Volatile Composition and Classification of Paeonia lactiflora Flower Aroma Types and Identification of the Fragrance-Related Genes. International journal of molecular sciences. 2023 May; 24(11):. doi: 10.3390/ijms24119410. [PMID: 37298360]
  • Aimé Vázquez, Nurhayat Tabanca, Paul E Kendra. HPTLC Analysis and Chemical Composition of Selected Melaleuca Essential Oils. Molecules (Basel, Switzerland). 2023 May; 28(9):. doi: 10.3390/molecules28093925. [PMID: 37175338]
  • Tian-Hao Pei, Yi-Jin Zhao, Sheng-Yuan Wang, Xiao-Feng Li, Chen-Qi Sun, Shu-Sen Shi, Meng-Lei Xu, Yu Gao. Preliminary Study on Insecticidal Potential and Chemical Composition of Five Rutaceae Essential Oils against Thrips flavus (Thysanoptera: Thripidae). Molecules (Basel, Switzerland). 2023 Mar; 28(7):. doi: 10.3390/molecules28072998. [PMID: 37049761]
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  • Miroslava Kačániová, Nenad L Vukovic, Natália Čmiková, Lucia Galovičová, Marianna Schwarzová, Veronika Šimora, Przemysław Łukasz Kowalczewski, Maciej Ireneusz Kluz, Czeslaw Puchalski, Ladislav Bakay, Milena D Vukic. Salvia sclarea Essential Oil Chemical Composition and Biological Activities. International journal of molecular sciences. 2023 Mar; 24(6):. doi: 10.3390/ijms24065179. [PMID: 36982252]
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