beta-Myrcene (BioDeep_00000000786)

 

Secondary id: BioDeep_00000859454

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H

化学式: C10H16 (136.1251936)
中文名称: 月桂烯, 香叶烯, 月桂烯
谱图信息: 最多检出来源 Macaca mulatta(otcml) 0.05%

分子结构信息

SMILES: C(=C)(C=C)CC/C=C(/C)\C
InChI: InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3

描述信息

7-Methyl-3-methylene-1,6-octadiene, also known as beta-Myrcene or myrcene is an acyclic monoterpene. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-erythritol-phosphate (MEP) pathway in the plastids. beta-Myrcene is a significant component of the essential oil of several plants, including allspice, bay, cannabis, hops, houttuynia, lemon grass, mango, myrcia, verbena, west indian bay tree, and cardamom. It is also the main component of wild thyme, the leaves of which contain up to 40\\\\% by weight of myrcene. Industrially, it is produced mainly semi-synthetically from myrcia, from which it gets its name. Myrcene has been detected as a volatile component in cannabis plant samples (PMID:26657499 ) and its essential oils (PMID:6991645 ). beta-Myrcene is the most abundant monoterpene in Cannabis and it has analgesic, anti-inflammatory, antibiotic, and antimutagenic activities. beta-Myrcene is a flavouring agent and it is used in the perfumery industry. It has a pleasant odor but is rarely used directly. It is a key intermediate in the production of several fragrances such as menthol, citral, citronellol, citronellal, geraniol, nerol, and linalool.
Myrcene, [liquid] appears as a yellow oily liquid with a pleasant odor. Flash point below 200 °F. Insoluble in water and less dense than water.
Beta-myrcene is a monoterpene that is octa-1,6-diene bearing methylene and methyl substituents at positions 3 and 7 respectively. It has a role as a plant metabolite, an anti-inflammatory agent, an anabolic agent, a fragrance, a flavouring agent and a volatile oil component.
Myrcene is a natural product found in Teucrium montanum, Xylopia aromatica, and other organisms with data available.
7-Methyl-3-methylene-1,6-octadiene is found in allspice. 7-Methyl-3-methylene-1,6-octadiene is found in many essential oils, e.g. hop oil. 7-Methyl-3-methylene-1,6-octadiene is a flavouring agent.
Myrcene is a metabolite found in or produced by Saccharomyces cerevisiae.
See also: Caraway Oil (part of); Mandarin oil (part of); Juniper Berry Oil (part of) ... View More ...
A monoterpene that is octa-1,6-diene bearing methylene and methyl substituents at positions 3 and 7 respectively.
Found in many essential oils, e.g. hop oil. Flavouring agent
Myrcene (β-Myrcene), an aromatic volatile compound, suppresses TNFα-induced NF-κB activity. Myrcene has anti-invasive effect[1][2].
Myrcene (β-Myrcene), an aromatic volatile compound, suppresses TNFα-induced NF-κB activity. Myrcene has anti-invasive effect[1][2].

同义名列表

59 个代谢物同义名

InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H; 7-Methyl-3-methylene-1,6-octadiene (beta -myrcene); Myrcene, primary pharmaceutical reference standard; 7-Methyl-3-methylene-1,6-octadiene (myrcene); 4-01-00-01108 (Beilstein Handbook Reference); 7-methyl-3-methylidene-octa-1,6-diene; Myrcene, >=95\\%, stabilized, FCC, FG; 7-methyl-3-methylideneocta-1,6-diene; 1,6-Octadiene, 7-methyl-3-methylene-; 7-Methyl-3-methyleneoctadiene-(1,6); 7-Methyl-3-methylene-octa-1,6-diene; 3-Methylene-7-methyl-1, 6-octadiene; 2-Methyl-6-methylene-2,7-octadiene; 3-Methylene-7-methyl-1,6-octadiene; 7-Methyl-3-methyleneocta-1,6-diene; 2-methyl-6-methylene-1,7-octadiene; 7-Methyl-3-methylene-1,6-octadiene; Octadiene, 7-methyl-3-methylene-; Methyl-3-methylene-1,6-octadiene; Methylene-7-methyl-1,6-octadiene; Methyl-6-methylene-2,7-octadiene; Myrcene (stabilized with BHT); Myrcene, analytical standard; Myrcene analytical standard; 1, 7-methyl-3-methylene-; Myrcene, technical grade; .BETA.-MYRCENE [IARC]; beta-MYRCENE (IARC); .BETA.-MYRCENE [MI]; WLN: 1Y1&U3YU1&1U1; |A-Myrcene (>90\\%); .beta.-Geraniolene; Myrcene (natural); ?-Myrcene (>90\\%); Myrcene, .beta.-; beta-geraniolene; UNII-3M39CZS25B; .beta.-Myrcene; MYRCENE [INCI]; MYRCENE [HSDB]; MYRCENE [FHFI]; β-Geraniolene; alpha-myrcene; beta -mircene; beta -myrcene; b-Geraniolene; MYRCENE [FCC]; beta-Mircene; beta-myrcene; Tox21_300351; 3M39CZS25B; Β-myrcene; α-myrcene; FEMA 2762; AI3-00738; b-Myrcene; Myrcene; N6Q; β-Myrcene



数据库引用编号

22 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

20 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(7)

WikiPathways(0)

Plant Reactome(4)

INOH(0)

PlantCyc(8)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

1391 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

  • 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]
  • Jinyu Zhou, Lingchao Kong, Debao Li, Xinxin Zhang, Zhijun Fu, Tengfei Pan, Yuan Yu. Nutritional and volatile profiles of pulp and flavedo from four local pummelo cultivars grown in Fujian province of China. Journal of food science. 2023 Aug; 88(8):3357-3372. doi: 10.1111/1750-3841.16701. [PMID: 37458289]
  • 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]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Maor Matzrafi, Shunamit Wolberg, Jackline Abu-Nassar, Einat Zelinger, Einat Bar, Daniella Cafri, Efraim Lewinsohn, Ilana Shtein. Distinctive foliar features and volatile profiles in three Ambrosia species (Asteraceae). Planta. 2023 Mar; 257(4):79. doi: 10.1007/s00425-023-04113-3. [PMID: 36912967]
  • Kaitlin Urso, William Vizuete, Ryan Moravec, Andrey Khlystov, Alicia Frazier, Glenn Morrison. Indoor Monoterpene Emission Rates from Commercial Cannabis Cultivation Facilities in Colorado. Journal of the Air & Waste Management Association (1995). 2023 Feb; ?(?):. doi: 10.1080/10962247.2023.2175741. [PMID: 36730104]
  • Saeeda Almarzooqi, Balaji Venkataraman, Vishnu Raj, Sultan Ali Abdulla Alkuwaiti, Karuna M Das, Peter D Collin, Thomas E Adrian, Sandeep B Subramanya. β-Myrcene Mitigates Colon Inflammation by Inhibiting MAP Kinase and NF-κB Signaling Pathways. Molecules (Basel, Switzerland). 2022 Dec; 27(24):. doi: 10.3390/molecules27248744. [PMID: 36557879]
  • Leila Gimenes, Júlio César R Lopes Silva, Roselaine Facanali, Leandro Wang Hantao, Walter José Siqueira, Marcia Ortiz Mayo Marques. Essential Oils of New Lippia alba Genotypes Analyzed by Flow-Modulated Comprehensive Two-Dimensional Gas Chromatography (GC×GC) and Chemometric Analysis. Molecules (Basel, Switzerland). 2021 Apr; 26(8):. doi: 10.3390/molecules26082332. [PMID: 33923848]
  • Pedro Soares-Castro, Filipa Soares, Pedro M Santos. Current Advances in the Bacterial Toolbox for the Biotechnological Production of Monoterpene-Based Aroma Compounds. Molecules (Basel, Switzerland). 2020 Dec; 26(1):. doi: 10.3390/molecules26010091. [PMID: 33379215]
  • Susan P Felter, Craig Llewelyn, Lisa Navarro, Xiaoling Zhang. How the 62-year old Delaney Clause continues to thwart science: Case study of the flavor substance β-myrcene. Regulatory toxicology and pharmacology : RTP. 2020 Aug; 115(?):104708. doi: 10.1016/j.yrtph.2020.104708. [PMID: 32522581]
  • Giulia Giunti, Orlando Campolo, Francesca Laudani, Giuseppe Massimo Algeri, Vincenzo Palmeri. Olive fruit volatiles route intraspecific interactions and chemotaxis in Bactrocera oleae (Rossi) (Diptera: Tephritidae) females. Scientific reports. 2020 02; 10(1):1666. doi: 10.1038/s41598-020-58379-8. [PMID: 32015351]
  • Pedro F S Toledo, Taciano P Ferreira, Isabela M A S Bastos, Sarah M Rezende, Luis O Viteri Jumbo, Julcemar Didonet, Bruno S Andrade, Tarcisio S Melo, Guy Smagghe, Eugênio E Oliveira, Raimundo W S Aguiar. Essential oil from Negramina (Siparuna guianensis) plants controls aphids without impairing survival and predatory abilities of non-target ladybeetles. Environmental pollution (Barking, Essex : 1987). 2019 Dec; 255(Pt 1):113153. doi: 10.1016/j.envpol.2019.113153. [PMID: 31520906]
  • Joel Ljunggren, Felipe Borrero-Echeverry, Amrita Chakraborty, Tobias U T Lindblom, Erik Hedenström, Maria Karlsson, Peter Witzgall, Marie Bengtsson. Yeast Volatomes Differentially Affect Larval Feeding in an Insect Herbivore. Applied and environmental microbiology. 2019 11; 85(21):. doi: 10.1128/aem.01761-19. [PMID: 31444202]
  • Tayyebeh Ghaffari, Hossein Samadi Kafil, Solmaz Asnaashari, Safar Farajnia, Abbas Delazar, Su Cheol Baek, Hamed Hamishehkar, Ki Hyun Kim. Chemical Composition and Antimicrobial Activity of Essential Oils from the Aerial Parts of Pinus eldarica Grown in Northwestern Iran. Molecules (Basel, Switzerland). 2019 Sep; 24(17):. doi: 10.3390/molecules24173203. [PMID: 31484421]
  • Xi Li, Dongqin Tang, Yimin Shi. Volatile compounds in perianth and corona of Narcissus Pseudonarcissus cultivars. Natural product research. 2019 Aug; 33(15):2281-2284. doi: 10.1080/14786419.2018.1499632. [PMID: 30375245]
  • Ramona Iseppi, Virginia Brighenti, Manuela Licata, Antonella Lambertini, Carla Sabia, Patrizia Messi, Federica Pellati, Stefania Benvenuti. Chemical Characterization and Evaluation of the Antibacterial Activity of Essential Oils from Fibre-Type Cannabis sativa L. (Hemp). Molecules (Basel, Switzerland). 2019 Jun; 24(12):. doi: 10.3390/molecules24122302. [PMID: 31234360]
  • Wanying He, Xiaoyan Li, Ying Peng, Xiaoyan He, Siyi Pan. Anti-Oxidant and Anti-Melanogenic Properties of Essential Oil from Peel of Pomelo cv. Guan Xi. Molecules (Basel, Switzerland). 2019 Jan; 24(2):. doi: 10.3390/molecules24020242. [PMID: 30634693]
  • J Fabbri, M A Maggiore, P E Pensel, C M Albani, G M Denegri, M C Elissondo. Could beta-myrcene be an alternative to albendazole for the treatment of experimental cystic echinococcosis?. Acta tropica. 2018 Nov; 187(?):5-12. doi: 10.1016/j.actatropica.2018.07.013. [PMID: 30040945]
  • Maria Bastaki, Michel Aubanel, Mark Bauter, Thierry Cachet, Jan Demyttenaere, Maodo Malick Diop, Christie L Harman, Shim-Mo Hayashi, Gerhard Krammer, Xiaodong Li, Craig Llewellyn, Odete Mendes, Kevin J Renskers, Jürgen Schnabel, Benjamin P C Smith, Sean V Taylor. Absence of renal adverse effects from β-myrcene dietary administration in OECD guideline-compliant subchronic toxicity study. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2018 Oct; 120(?):222-229. doi: 10.1016/j.fct.2018.07.004. [PMID: 30017998]
  • Cinzia Formighieri, Anastasios Melis. Cyanobacterial production of plant essential oils. Planta. 2018 Oct; 248(4):933-946. doi: 10.1007/s00425-018-2948-0. [PMID: 29974209]
  • Jiao Xie, Lili Deng, Yahan Zhou, Shixiang Yao, Kaifang Zeng. Analysis of changes in volatile constituents and expression of genes involved in terpenoid metabolism in oleocellosis peel. Food chemistry. 2018 Mar; 243(?):269-276. doi: 10.1016/j.foodchem.2017.09.142. [PMID: 29146338]
  • Dongyu Gu, Chen Fang, Jiao Yang, Minjing Li, Hengming Liu, Yi Yang. Chemical composition and α-amylase inhibitory activity of the essential oil from Sabina chinensis cv. Kaizuca leaves. Natural product research. 2018 Mar; 32(6):711-713. doi: 10.1080/14786419.2017.1332612. [PMID: 28539061]
  • Vincent O Nyasembe, David P Tchouassi, Christian W W Pirk, Catherine L Sole, Baldwyn Torto. Host plant forensics and olfactory-based detection in Afro-tropical mosquito disease vectors. PLoS neglected tropical diseases. 2018 02; 12(2):e0006185. doi: 10.1371/journal.pntd.0006185. [PMID: 29462150]
  • Hui Liu, Zhen-Long Wu, Xiao-Jun Huang, Yinghui Peng, Xiaojie Huang, Lei Shi, Ying Wang, Wen-Cai Ye. Evaluation of Diarylheptanoid-Terpene Adduct Enantiomers from Alpinia officinarum for Neuroprotective Activities. Journal of natural products. 2018 01; 81(1):162-170. doi: 10.1021/acs.jnatprod.7b00803. [PMID: 29323912]
  • Yi-Tien Chiu, Hsin-Chun Chen, Chen Chang. The Variation of Oncidium Rosy Sunset Flower Volatiles with Daily Rhythm, Flowering Period, and Flower Parts. Molecules (Basel, Switzerland). 2017 Sep; 22(9):. doi: 10.3390/molecules22091468. [PMID: 28869565]
  • Abolfazl Shakeri, Javad Akhtari, Vahid Soheili, Seyedeh Faezeh Taghizadeh, Amirhossein Sahebkar, Rezvan Shaddel, Javad Asili. Identification and biological activity of the volatile compounds of Glycyrrhiza triphylla Fisch. & C.A.Mey. Microbial pathogenesis. 2017 Aug; 109(?):39-44. doi: 10.1016/j.micpath.2017.05.022. [PMID: 28526637]
  • Babak Abdollahi Mandoulakani, Elham Eyvazpour, Morteza Ghadimzadeh. The effect of drought stress on the expression of key genes involved in the biosynthesis of phenylpropanoids and essential oil components in basil (Ocimum basilicum L.). Phytochemistry. 2017 Jul; 139(?):1-7. doi: 10.1016/j.phytochem.2017.03.006. [PMID: 28366608]
  • Pedro Soares-Castro, Pedro Montenegro-Silva, Hermann J Heipieper, Pedro M Santos. Functional Characterization of a 28-Kilobase Catabolic Island from Pseudomonas sp. Strain M1 Involved in Biotransformation of β-Myrcene and Related Plant-Derived Volatiles. Applied and environmental microbiology. 2017 05; 83(9):. doi: 10.1128/aem.03112-16. [PMID: 28213543]
  • C E S Carvalho, E P C Sobrinho-Junior, L M Brito, L A D Nicolau, T P Carvalho, A K S Moura, K A F Rodrigues, S M P Carneiro, D D R Arcanjo, A M G L Citó, F A A Carvalho. Anti-Leishmania activity of essential oil of Myracrodruon urundeuva (Engl.) Fr. All.: Composition, cytotoxity and possible mechanisms of action. Experimental parasitology. 2017 Apr; 175(?):59-67. doi: 10.1016/j.exppara.2017.02.012. [PMID: 28189487]
  • Judith K Booth, Jonathan E Page, Jörg Bohlmann. Terpene synthases from Cannabis sativa. PloS one. 2017; 12(3):e0173911. doi: 10.1371/journal.pone.0173911. [PMID: 28355238]
  • F Sadeghian, P Ebrahimi, A Shakeri, M R Jamali. Extraction of Citrus paradisi Volatile Components by Headspace Single-Drop Microextraction and Statistical Modeling. Journal of chromatographic science. 2016 Aug; 54(7):1263-9. doi: 10.1093/chromsci/bmw038. [PMID: 27048646]
  • L Irene Terry, Robert B Roemer, David T Booth, Chris J Moore, Gimme H Walter. Thermogenic respiratory processes drive the exponential increase of volatile organic compound emissions in Macrozamia cycad cones. Plant, cell & environment. 2016 07; 39(7):1588-600. doi: 10.1111/pce.12730. [PMID: 26924274]
  • Yan Qian, Sheng Yu, Ming-Qiu Shan, Wei-Feng Yao, Li Zhang. [Comparison between traditional processing and integration processing for Schizonepetae Herba based on chemical constituents and pharmacological effect]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2016 Jun; 41(11):2081-2086. doi: 10.4268/cjcmm20161117. [PMID: 28901104]
  • Srdjan Bojović, Maja Jurc, Mihailo Ristić, Zorica Popović, Rada Matić, Vera Vidaković, Milena Stefanović, Dušan Jurc. Essential-Oil Variability in Natural Populations of Pinus mugo Turra from the Julian Alps. Chemistry & biodiversity. 2016 Feb; 13(2):181-7. doi: 10.1002/cbdv.201500029. [PMID: 26880430]
  • Hossein Mahmoudvand, Farnaz Kheirandish, Mehdi Ghasemi Kia, Amir Tavakoli Kareshk, Mohammad Yarahmadi. Chemical composition, protoscolicidal effects and acute toxicity of Pistacia atlantica Desf. fruit extract. Natural product research. 2016; 30(10):1208-11. doi: 10.1080/14786419.2015.1046868. [PMID: 26252652]
  • Se Yeon Oh. An Effective Quality Control of Pharmacologically Active Volatiles of Houttuynia cordata Thunb by Fast Gas Chromatography-Surface Acoustic Wave Sensor. Molecules (Basel, Switzerland). 2015 Jun; 20(6):10298-312. doi: 10.3390/molecules200610298. [PMID: 26046325]
  • Detlef Ulrich, Thomas Nothnagel, Hartwig Schulz. Influence of cultivar and harvest year on the volatile profiles of leaves and roots of carrots (Daucus carota spp. sativus Hoffm.). Journal of agricultural and food chemistry. 2015 Apr; 63(13):3348-56. doi: 10.1021/acs.jafc.5b00704. [PMID: 25797828]
  • Pedro Soares-Castro, Pedro M Santos. Deciphering the genome repertoire of Pseudomonas sp. M1 toward β-myrcene biotransformation. Genome biology and evolution. 2014 Dec; 7(1):1-17. doi: 10.1093/gbe/evu254. [PMID: 25503374]
  • Kelsey J R P Byers, James P Vela, Foen Peng, Jeffrey A Riffell, Harvey D Bradshaw. Floral volatile alleles can contribute to pollinator-mediated reproductive isolation in monkeyflowers (Mimulus). The Plant journal : for cell and molecular biology. 2014 Dec; 80(6):1031-42. doi: 10.1111/tpj.12702. [PMID: 25319242]
  • Marie Marchini, Céline Charvoz, Laurence Dujourdy, Nicolas Baldovini, Jean-Jacques Filippi. Multidimensional analysis of cannabis volatile constituents: identification of 5,5-dimethyl-1-vinylbicyclo[2.1.1]hexane as a volatile marker of hashish, the resin of Cannabis sativa L. Journal of chromatography. A. 2014 Nov; 1370(?):200-15. doi: 10.1016/j.chroma.2014.10.045. [PMID: 25454145]
  • Zeynep Ulukanli, Salih Karabörklü, Fuat Bozok, Menderes Çenet, Bintuğ Oztürk, Mehmet Balcilar. Antimicrobial, insecticidal and phytotoxic activities of Cotinus coggyria Scop. essential oil (Anacardiaceae). Natural product research. 2014; 28(23):2150-7. doi: 10.1080/14786419.2014.928879. [PMID: 24980636]
  • Hoang D Trung, Tran D Thang, Pham H Ban, Tran M Hoi, Do N Dai, Isiaka A Ogunwande. Terpene constituents of the leaves of five Vietnamese species of Clausena (Rutaceae). Natural product research. 2014; 28(9):622-30. doi: 10.1080/14786419.2014.888555. [PMID: 24617735]
  • Do N Dai, Le T Huong, Tran D Thang, Isiaka A Ogunwande. Analysis of essential oil constituents of three Dasymaschalon species (Annonaceae) from Vietnam. Natural product research. 2014; 28(3):156-63. doi: 10.1080/14786419.2013.858339. [PMID: 24236527]
  • Mark F Cesta, Gordon C Hard, John T Boyce, Michael J Ryan, Po C Chan, Robert C Sills. Complex histopathologic response in rat kidney to oral β-myrcene: an unusual dose-related nephrosis and low-dose alpha2u-globulin nephropathy. Toxicologic pathology. 2013; 41(8):1068-77. doi: 10.1177/0192623313482057. [PMID: 23531794]
  • Tran D Thang, Le T Huong, Do N Dai, Isiaka A Ogunwande. A comparative analysis of essential oils of Goniothalamus macrocalyx Ban., Goniothalamus albiflorus Ban. and Goniothalamus tamirensis Pierre ex Fin. & Gagnep. from Vietnam. Natural product research. 2013; 27(21):1999-2005. doi: 10.1080/14786419.2013.814051. [PMID: 23822670]
  • Rajendra C Padalia, Ram S Verma, Amit Chauhan, Chandan S Chanotiya. Chemical composition of leaf and root essential oils of Boenninghausenia albiflora Reichb. from northern India. Natural product research. 2012 Nov; 26(21):2040-4. doi: 10.1080/14786419.2011.635344. [PMID: 22111591]
  • C Messaoud, H Chograni, M Boussaid. Chemical composition and antioxidant activities of essential oils and methanol extracts of three wild Lavandula L. species. Natural product research. 2012 Nov; 26(21):1976-84. doi: 10.1080/14786419.2011.635343. [PMID: 22117129]
  • Frauke Lüddeke, Aytac Dikfidan, Jens Harder. Physiology of deletion mutants in the anaerobic β-myrcene degradation pathway in Castellaniella defragrans. BMC microbiology. 2012 Sep; 12(?):192. doi: 10.1186/1471-2180-12-192. [PMID: 22947208]
  • Eunae Kim, Il-Kwon Park. Fumigant antifungal activity of Myrtaceae essential oils and constituents from Leptospermum petersonii against three Aspergillus species. Molecules (Basel, Switzerland). 2012 Sep; 17(9):10459-69. doi: 10.3390/molecules170910459. [PMID: 22945026]
  • Clécio S Ramos, Marisi G Soares, Adalberto M da Silva, Luciane G Batista-Pereira, Arlene G Corrêa, Massuo J Kato. Electrophysiological responses of the Naupactus bipes beetle to essential oils from Piperaceae species. Natural product communications. 2012 Aug; 7(8):1103-6. doi: ". [PMID: 22978240]
  • Nadir Erbilgin, L Jessie Colgan. Differential effects of plant ontogeny and damage type on phloem and foliage monoterpenes in jack pine (Pinus banksiana). Tree physiology. 2012 Aug; 32(8):946-57. doi: 10.1093/treephys/tps047. [PMID: 22659460]
  • Yan Yvon, Emmanuel Guy Raoelison, René Razafindrazaka, Adolphe Randriantsoa, Mehrez Romdhane, Naziha Chabir, Mounira Guedri Mkaddem, Jalloul Bouajila. Relation between chemical composition or antioxidant activity and antihypertensive activity for six essential oils. Journal of food science. 2012 Aug; 77(8):H184-91. doi: 10.1111/j.1750-3841.2012.02812.x. [PMID: 22860587]
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