(-)-alpha-Pinene (BioDeep_00000000774)

Main id: BioDeep_00000014901

Secondary id: BioDeep_00000872585

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


(-)-alpha-Pinene, 99\\%, optical purity ee: >=86\\% (GLC)

化学式: C10H16 (136.1251936)
中文名称: (±)-2-蒎烯, (-)-α-蒎烯, 左旋-α-蒎烯, 2-蒎烯, 左旋-alpha-蒎烯
谱图信息: 最多检出来源 unclassified Codonopsis(otcml) 75%

分子结构信息

SMILES: C1([C@@H]2C(=CC[C@H]1C2)C)(C)C
InChI: InChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9-/m0/s1

描述信息

(-)-alpha-pinene is an alpha-pinene. It is an enantiomer of a (+)-alpha-pinene.
(-)-alpha-Pinene is a natural product found in Curcuma amada, Thryptomene saxicola, and other organisms with data available.
(-)-alpha-Pinene is found in almond. alpha-Pinene is an organic compound of the terpene class, one of two isomers of pinene. It is found in the oils of many species of many coniferous trees, notably the pine. It is also found in the essential oil of rosemary (Rosmarinus officinalis). Both enantiomers are known in nature; 1S,5S- or (-)-alpha-pinene is more common in European pines, whereas the 1R,5R- or (+)-alpha-isomer is more common in North America. The racemic mixture is present in some oils such as eucalyptus oil. (Wikipedia) (-)-alpha-Pinene belongs to the family of Bicyclic Monoterpenes. These are monoterpenes containing exactly 2 rings, which are fused to each other.
alpha-Pinene (CAS: 80-56-8) is an organic compound of the terpene class and is one of two isomers of pinene. It is found in the oils of many species of many coniferous trees, notably the pine. It is also found in the essential oil of rosemary (Rosmarinus officinalis). Both enantiomers are known in nature. 1S,5S- or (-)-alpha-pinene is more common in European pines, whereas the 1R,5R- or (+)-alpha-isomer is more common in North America. The racemic mixture is present in some oils such as eucalyptus oil (Wikipedia). (-)-alpha-Pinene is found in almond.
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].
(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1].

同义名列表

83 个代谢物同义名

(-)-alpha-Pinene, 99\\%, optical purity ee: >=86\\% (GLC); (-)-alpha-Pinene, 98\\%, optical purity ee: >=81\\% (GLC); (-)-alpha-Pinene, 99\\%, optical purity ee: 97\\% (GLC); Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1S,5S)-; Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, (1S,5S)-; Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, (1S,5S)-; Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, (1S)-; (1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-ene; (1S,5S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; 4,6,6-Trimethylbicyklo(3,1,1)hept-3-en [Czech]; (1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; 4-05-00-00456 (Beilstein Handbook Reference); Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl; 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; (-)-alpha-Pinene, analytical standard; (-)-alpha-Pinene, >=97\\%, FCC, FG; GRWFGVWFFZKLTI-IUCAKERBSA-N; (1S,5S)-(-)-.ALPHA.-PINENE; (-)-(1S,5S)-alpha-pinene; (1S,5S)-(-)-alpha-Pinene; (1S)-(-)-.alpha.-Pinene; (-)-(1S)-.ALPHA.-PINENE; alpha-Pinene (natural); 2-Pinene, (1S,5S)-(-)-; 1S,5S-(-)-alpha-Pinene; .ALPHA.-PINENE, (+/-)-; (S)-(-)-.ALPHA.-PINENE; (-)-(1S)-alpha-Pinene; .ALPHA.-PINENE [FHFI]; (1S)-(-)-alpha-Pinene; alpha-pinene, pinene; (+/-)-.ALPHA.-PINENE; (1S,5S)-(-)-Α-pinene; (S)-(-)-alpha-Pinene; (1S,5S)-alpha-pinene; ALPHA-PINENE [HSDB]; .ALPHA.-PINENE [MI]; (-)-.alpha.-Pinene; .ALPHA.-PINENE-(-); (1S)-(-)-|A-Pinene; .ALPHA.-PINENE, L-; ALPHA-PINENE [FCC]; alpha-Pinene, (-)-; (-)- alpha -Pinene; (1S)-(-)-Α-pinene; 1S-.alpha.-Pinene; (1S,5S)-pin-2-ene; (1S)-(-)-a-Pinene; Alpha-Pinene ,(S); (-)-(1S)-Α-pinene; (-)-Pin-2(3)-ene; (1S,5S)-Α-pinene; (-)-alpha-Pinene; L-.alpha.-Pinene; (S)-(-)-Α-pinene; (1S,5S)-a-Pinene; (±)-alpha-Pinene; DL-ALPHA-PINENE; UNII-TZR3GM95PR; UNII-JPF3YI7O34; DL-Pin-2(3)-ene; 1S-alpha-Pinene; 1S-(-)-a-Pinene; (S)-(-)-Pinene; (-)-|A-pinene; (-)-a-pinene; Tox21_303591; (±)-2-Pinene; (±)-α-Pinene; Tox21_201760; (-)-α-Pinene; (-)-2-Pinene; alpha-pinene; 1S-a-Pinene; 1S-Α-pinene; JPF3YI7O34; L-a-Pinene; (-)--inene; TZR3GM95PR; AI3-24594; Wilt Pruf; 2-pinene; α-Pinene



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(0)

PlantCyc(0)

代谢反应

27 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(6)

WikiPathways(0)

Plant Reactome(4)

INOH(0)

PlantCyc(16)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

105 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

  • John Staton Laws, Scott D Smid. Characterizing cannabis-prevalent terpenes for neuroprotection reveal a role for α and β-pinenes in mitigating amyloid β-evoked neurotoxicity and aggregation in vitro. Neurotoxicology. 2024 Jan; 100(?):16-24. doi: 10.1016/j.neuro.2023.12.004. [PMID: 38070653]
  • Mingyu Xue, Xiaohong Xia, Yadi Deng, Fei Teng, Shiyue Zhao, Hui Li, Dejun Hao, Wei-Yi Chen. Identification and Functional Analysis of an Epsilon Class Glutathione S-Transferase Gene Associated with α-Pinene Adaptation in Monochamus alternatus. International journal of molecular sciences. 2023 Dec; 24(24):. doi: 10.3390/ijms242417376. [PMID: 38139205]
  • Neby M Mérida-Torres, Leopoldo Cruz-López, Edi A Malo, Samuel Cruz-Esteban. Attraction of the two-spotted spider mite, Tetranychus urticae (Acari: Tetranychidae), to healthy and damaged strawberry plants mediated by volatile cues. Experimental & applied acarology. 2023 Nov; 91(3):413-427. doi: 10.1007/s10493-023-00852-w. [PMID: 37861891]
  • Noura S Dosoky, Liliya N Kirpotina, Igor A Schepetkin, Andrei I Khlebnikov, Brent L Lisonbee, Jeffrey L Black, Hillary Woolf, Trever L Thurgood, Brittany L Graf, Prabodh Satyal, Mark T Quinn. Volatile Composition, Antimicrobial Activity, and In Vitro Innate Immunomodulatory Activity of Echinacea purpurea (L.) Moench Essential Oils. Molecules (Basel, Switzerland). 2023 Oct; 28(21):. doi: 10.3390/molecules28217330. [PMID: 37959750]
  • Lexiao Jin, Zhengzhi Xie, Pawel Lorkiewicz, Sanjay Srivastava, Aruni Bhatnagar, Daniel J Conklin. Endothelial-dependent Relaxation of Alpha-Pinene and Two Metabolites, Myrtenol and Verbenol, in Isolated Murine Blood Vessels. American journal of physiology. Heart and circulatory physiology. 2023 Oct; ?(?):. doi: 10.1152/ajpheart.00380.2023. [PMID: 37889254]
  • Huizhong Hu, Dengwu Li, Ruxue Bai, Weiping Zhang, Hong Luo, Enping Yu. Chemodiversity and Bioactivity of the Essential Oils of Juniperus and Implication for Taxonomy. International journal of molecular sciences. 2023 Oct; 24(20):. doi: 10.3390/ijms242015203. [PMID: 37894884]
  • Yessenia E Maldonado, Omar Malagón, Nixon Cumbicus, Gianluca Gilardoni. A new essential oil from the native Ecuadorian species Steiractinia sodiroi (Hieron.) S.F. Blake (Asteraceae): chemical and enantioselective analyses. Scientific reports. 2023 Oct; 13(1):17180. doi: 10.1038/s41598-023-44524-6. [PMID: 37821569]
  • Ji-Hong Park, Min-Jung Huh, Jae-Woo Lee, Min-Woo Lee, Dong-Ho Lee, Il Nam, Il-Kwon Park. Seasonal occurrence of bark and woodboring Coleoptera in stands of Pinus densiflora (Pinales: Pinaceae) and Larix kaempferi (Pinales: Pinaceae) and monitoring method using multifunnel traps baited with pine volatiles. Journal of economic entomology. 2023 Sep; ?(?):. doi: 10.1093/jee/toad175. [PMID: 37774406]
  • Yan Jiang, Chunli Xiu, Hongsheng Pan, Xiaoning Liu. Recruitment of Hippodamia variegata by active volatiles from Glycyrrhiza uralensis and Alhagi sparsifolia plants infested with Aphis atrata. Pest management science. 2023 Sep; ?(?):. doi: 10.1002/ps.7765. [PMID: 37691614]
  • Junming Sun, Kexin Tian, Lu Jing, Yafei Niu, Qian Lou, Hongwu Chen. Identification of characteristic aroma compounds for spicy in Iris lactea var. chinensis. Physiologia plantarum. 2023 Sep; 175(5):e14016. doi: 10.1111/ppl.14016. [PMID: 37882258]
  • Jane Marie N Caasi, Raiza Isabel D G Baldoza, Mary Sophia C Bauzon, Mirabella Anne F Odtohan, Librado A Santiago, Myla R Santiago-Bautista. In Silico Prediction of Selected Bioactive Compounds Present in Alpinia elegans (C.Presl) K.Schum Seed Oil as Potential Drug Candidates Against Human Cancer Cell Lines. Asian Pacific journal of cancer prevention : APJCP. 2023 Aug; 24(8):2601-2614. doi: 10.31557/apjcp.2023.24.8.2601. [PMID: 37642045]
  • Jingxin Cao, Xin Hao, Yang Li, Ruina Tan, Zhixin Cui, Lu Li, Yue Zhang, Jingyu Cao, Mengru Min, Liwei Liang, Zhe Xu, Wei Ma, Ling Ma. Exploring the role of detoxification genes in the resistance of Bursaphelenchus xylophilus to different exogenous nematicidal substances using transcriptomic analyses. Pesticide biochemistry and physiology. 2023 Aug; 194(?):105527. doi: 10.1016/j.pestbp.2023.105527. [PMID: 37532336]
  • Riham A El-Shiekh, Hanaa A H Kassem, Amal E Khaleel, Menna M A Abd El-Mageed. Anticholinesterases activity of Murraya koenigii (L.) Spreng. and Murraya paniculata (L.) Jacq. essential oils with GC/MS analysis and molecular docking. Natural product research. 2023 Jul; ?(?):1-5. doi: 10.1080/14786419.2023.2241150. [PMID: 37516925]
  • 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]
  • Mahmood R Nikbakhtzadeh. A synthetic lure for Anopheles gambiae (Diptera: Culicidae) based on the attractive plant Parthenium hysterophorus. Journal of medical entomology. 2023 Jun; ?(?):. doi: 10.1093/jme/tjad077. [PMID: 37364179]
  • Maria Nancy N de Lima, Jamile Silva da Costa, Bruna A Guimarães, Jofre Jacob S Freitas, William N Setzer, Joyce Kelly R da Silva, José Guilherme S Maia, Pablo Luis B Figueiredo. Chemometrics of the Composition and Antioxidant Capacity of Hyptis crenata Essential Oils from Brazil. Molecules (Basel, Switzerland). 2023 Apr; 28(8):. doi: 10.3390/molecules28083371. [PMID: 37110606]
  • Zinnat Shahina, Ragothaman M Yennamalli, Tanya E S Dahms. Key essential oil components delocalize Candida albicans Kar3p and impact microtubule structure. Microbiological research. 2023 Apr; 272(?):127373. doi: 10.1016/j.micres.2023.127373. [PMID: 37058783]
  • Jean-Luc Boevé, Gontran Sonet, Herbert R Jacobson, Sergio Angeli. Cypress terpenes in sawfly larva of Susana cupressi (Hymenoptera: Symphyta: Tenthredinoidea). Die Naturwissenschaften. 2023 Mar; 110(2):13. doi: 10.1007/s00114-023-01841-0. [PMID: 36971882]
  • James Calva, Luis Cartuche, Leydy Nathaly Castillo, Vladimir Morocho. Biological Activities and Chemical Composition of Essential Oil from Hedyosmum purpurascens (Todzia)-An Endemic Plant in Ecuador. Molecules (Basel, Switzerland). 2023 Mar; 28(5):. doi: 10.3390/molecules28052366. [PMID: 36903611]
  • Gaia Stringari, Joan Villanueva, Antoni Rosell-Melé, Nuria Moraleda-Cibrián, Francesco Orsini, Gara Villalba, Xavier Gabarrell. Assessment of greenhouse emissions of the green bean through the static enclosure technique. The Science of the total environment. 2023 Feb; ?(?):162319. doi: 10.1016/j.scitotenv.2023.162319. [PMID: 36801412]
  • Xu-Yi Ling, Xiao-Jing Lin, Lin-Xuan Huang, Peng Yang, Jin-Fen Yang. [Comparison of catalytic functions and expression patterns of two pinene synthases from Wurfbainia villosa]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2023 Feb; 48(3):642-648. doi: 10.19540/j.cnki.cjcmm.20221101.103. [PMID: 36872227]
  • Helia Rahmani, Mohammad Raman Moloudi, Paria Hashemi, Kambiz Hassanzadeh, Esmael Izadpanah. Alpha-Pinene Alleviates Motor Activity in Animal Model of Huntington's Disease via Enhancing Antioxidant Capacity. Neurochemical research. 2023 Jan; ?(?):. doi: 10.1007/s11064-023-03860-9. [PMID: 36689085]
  • Guangchao Cui, Xiang Zhou, Qian Wang, Kai Zhang, Lei Qin, Jixing Guo. The Sequence Characteristics and Binding Properties of the Odorant-Binding Protein 2 of Euplatypus parallelus to Semiochemicals. International journal of molecular sciences. 2023 Jan; 24(2):. doi: 10.3390/ijms24021714. [PMID: 36675226]
  • Maria Nancy N de Lima, Bruna A Guimarães, Ana Lídia S de Castro, Kevellen B Ribeiro, Daniele C Miller, Pedro Iuri C da Silva, Jofre Jacob S Freitas, Anderson B de Lima, William N Setzer, Joyce Kelly R da Silva, José Guilherme S Maia, Pablo Luis B Figueiredo. Chemical composition and antinociceptive and anti-inflammatory activity of the essential oil of Hyptis crenata Pohl ex Benth. from the Brazilian Amazon. Journal of ethnopharmacology. 2023 Jan; 300(?):115720. doi: 10.1016/j.jep.2022.115720. [PMID: 36113677]
  • Yeqin Huang, Heran Xu, Mengting Ding, Jingyi Li, Di Wang, Hui Li, Meiyu Sun, Fei Xia, Hongtong Bai, Min Wang, Meiling Mo, Lei Shi. Screening of Rosemary Essential Oils with Different Phytochemicals for Antioxidant Capacity, Keratinocyte Cytotoxicity, and Anti-Proliferative Activity. Molecules (Basel, Switzerland). 2023 Jan; 28(2):. doi: 10.3390/molecules28020586. [PMID: 36677644]
  • Yongquan Li, Yanfang Gao, Lin Deng, Huiming Lian, Wei Guo, Wei Wu, Bine Xue, Baobin Li, Yuzhen Su, Hui Zhang. Volatile Profiling and Transcriptome Sequencing Provide Insights into the Biosynthesis of α-Pinene and β-Pinene in Liquidambar formosana Hance Leaves. Genes. 2023 Jan; 14(1):. doi: 10.3390/genes14010163. [PMID: 36672904]
  • Saeid Gasemi, Hassan Mahdavikia, Esmaeil Rezaei-Chiyaneh, Farzad Banaei-Asl, Aria Dolatabadian, Amir Sadeghpour. Co-inoculation of mycorrhizal fungi and plant growth-promoting rhizobacteria improve growth, biochemical and physiological attributes in Dracocephalum kotschyi Boiss. under water deficit stress. PeerJ. 2023; 11(?):e16474. doi: 10.7717/peerj.16474. [PMID: 38047030]
  • Sudipta Jena, Asit Ray, Omprakash Mohanta, Prabhat Kumar Das, Ambika Sahoo, Sanghamitra Nayak, Pratap Chandra Panda. Neocinnamomum caudatum Essential Oil Ameliorates Lipopolysaccharide-Induced Inflammation and Oxidative Stress in RAW 264.7 Cells by Inhibiting NF-κB Activation and ROS Production. Molecules (Basel, Switzerland). 2022 Nov; 27(23):. doi: 10.3390/molecules27238193. [PMID: 36500283]
  • Mohammad Mahdi Karimkhani, Mahmoud Nasrollahzadeh, Mehdi Maham, Abdollah Jamshidi, Mohammad Saeed Kharazmi, Danial Dehnad, Seid Mahdi Jafari. Extraction and purification of α-pinene; a comprehensive review. Critical reviews in food science and nutrition. 2022 Nov; ?(?):1-26. doi: 10.1080/10408398.2022.2140331. [PMID: 36384372]
  • Bin Liu, Hui Chen. Disruption of CYP6DF1 and CYP6DJ2 increases the susceptibility of Dendroctonus armandi to (+)-α-pinene. Pesticide biochemistry and physiology. 2022 Nov; 188(?):105270. doi: 10.1016/j.pestbp.2022.105270. [PMID: 36464375]
  • Bin Liu, Danyang Fu, Hang Ning, Ming Tang, Hui Chen. Knockdown of CYP6CR2 and CYP6DE5 reduces tolerance to host plant allelochemicals in the Chinese white pine beetle Dendroctonus armandi. Pesticide biochemistry and physiology. 2022 Oct; 187(?):105180. doi: 10.1016/j.pestbp.2022.105180. [PMID: 36127042]
  • Bin Liu, Ming Tang, Hui Chen. Activation of the ROS/CncC Signaling Pathway Regulates Cytochrome P450 CYP4BQ1 Responsible for (+)-α-Pinene Tolerance in Dendroctonus armandi. International journal of molecular sciences. 2022 Sep; 23(19):. doi: 10.3390/ijms231911578. [PMID: 36232876]
  • Rajnish Srivastava, Pratim K Choudhury, Suresh Kumar Dev, Vaibhav Rathore. Formulation and Evaluation of α-Pinene Loaded Self-emulsifying Nanoformulation for In-Vivo Anti-Parkinson's Activity. Recent patents on nanotechnology. 2022; 16(2):139-159. doi: 10.2174/1872210515666210329161439. [PMID: 33781196]
  • Mengci Chen, Youming Qiao, Xiaolong Quan, Huilan Shi, Zhonghua Duan. Physiological, biochemical and phytohormone responses of Elymus nutans to α-pinene-induced allelopathy. PeerJ. 2022; 10(?):e14100. doi: 10.7717/peerj.14100. [PMID: 36196396]
  • Zinnat Shahina, Raymond Al Homsi, Jared D W Price, Malcolm Whiteway, Taranum Sultana, Tanya E S Dahms. Rosemary essential oil and its components 1,8-cineole and α-pinene induce ROS-dependent lethality and ROS-independent virulence inhibition in Candida albicans. PloS one. 2022; 17(11):e0277097. doi: 10.1371/journal.pone.0277097. [PMID: 36383525]
  • Salman S Alharthi, Ahmed Noah Badr, Karolina Gromadzka, Kinga Stuper-Szablewska, Adel Gabr Abdel-Razek, Khaled Selim. Bioactive Molecules of Mandarin Seed Oils Diminish Mycotoxin and the Existence of Fungi. Molecules (Basel, Switzerland). 2021 Nov; 26(23):. doi: 10.3390/molecules26237130. [PMID: 34885712]
  • Tianming Zhao, Chao Ma, Guofei Zhu. Chemical Composition and Biological Activities of Essential Oils from the Leaves, Stems, and Roots of Kadsura coccinea. Molecules (Basel, Switzerland). 2021 Oct; 26(20):. doi: 10.3390/molecules26206259. [PMID: 34684838]
  • Alexis St-Gelais, Eliana M Maldonado, Gloria Saavedra, Samuel Siles-Alvarado, Jérôme Alsarraf, Guy Collin, André Pichette. Essential Oils from Bolivia. XV. Herzogole, an Original Monoterpene Benzodioxole from an Essential Oil from Pentacalia herzogii (Cabrera) Cuatrec. Molecules (Basel, Switzerland). 2021 Sep; 26(19):. doi: 10.3390/molecules26195766. [PMID: 34641307]
  • Rajashri R Naik, Ashok K Shakya, Benedetta Ferri, Ghaleb A Oriquat, Luisa Pistelli, Nawfal A M Numan. Volatile Composition and Biological Activity of Jordanian Commercial Samples of R. coriaria L. Fruits. Molecules (Basel, Switzerland). 2021 Sep; 26(18):. doi: 10.3390/molecules26185691. [PMID: 34577162]
  • Xuan Song, Yao-Guo Qin, Yue Yin, Zheng-Xi Li. Identification and Behavioral Assays of Alarm Pheromone in the Vetch Aphid Megoura viciae. Journal of chemical ecology. 2021 Sep; 47(8-9):740-746. doi: 10.1007/s10886-021-01297-4. [PMID: 34347235]
  • Eduardo Valarezo, Vladimir Morocho, Luis Cartuche, Fernanda Chamba-Granda, Magdaly Correa-Conza, Ximena Jaramillo-Fierro, Miguel Angel Meneses. Variability of the Chemical Composition and Bioactivity between the Essential Oils Isolated from Male and Female Specimens of Hedyosmum racemosum (Ruiz & Pav.) G. Don. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154613. [PMID: 34361766]
  • Zenab Aly Torky, Ashaimaa Y Moussa, Eman A Abdelghffar, Usama K Abdel-Hameed, Omayma A Eldahshan. Chemical profiling, antiviral and antiproliferative activities of the essential oil of Phlomis aurea Decne grown in Egypt. Food & function. 2021 May; 12(10):4630-4643. doi: 10.1039/d0fo03417g. [PMID: 33912870]
  • Judith Salas-Oropeza, Manuel Jimenez-Estrada, Armando Perez-Torres, Andres Eliu Castell-Rodriguez, Rodolfo Becerril-Millan, Marco Aurelio Rodriguez-Monroy, Katia Jarquin-Yañez, Maria Margarita Canales-Martinez. Wound Healing Activity of α-Pinene and α-Phellandrene. Molecules (Basel, Switzerland). 2021 Apr; 26(9):. doi: 10.3390/molecules26092488. [PMID: 33923276]
  • Liucija Kamaitytė-Bukelskienė, Kristina Ložienė, Juozas Labokas. Dynamics of Isomeric and Enantiomeric Fractions of Pinene in Essential Oil of Picea abies Annual Needles during Growing Season. Molecules (Basel, Switzerland). 2021 Apr; 26(8):. doi: 10.3390/molecules26082138. [PMID: 33917721]
  • Assia Zeghib, Claude-Alain Calliste, Alain Simon, Rim Charfeddine, Mahjoub Aouni, Jean-Luc Duroux, Ahmed Kabouche, Zahia Kabouche. Chemical composition and biological potential of Thymus Willdenowii Boiss. & Reut. essential oil. Natural product research. 2021 Mar; 35(5):845-848. doi: 10.1080/14786419.2019.1602830. [PMID: 30990332]
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