Carene (BioDeep_00000395620)

 

Secondary id: BioDeep_00000007629, BioDeep_00000016650, BioDeep_00000858573, BioDeep_00000859519

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


(+)-3-delta-Carene, primary pharmaceutical reference standard

化学式: C10H16 (136.1252)
中文名称: (1S)-(+)-3-蒈烯, (+)-3-蒈烯, 3-卡琳, 3-蒈烯
谱图信息: 最多检出来源 Viridiplantae(plant) 13.31%

分子结构信息

SMILES: CC1=CCC2C(C1)C2(C)C
InChI: InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3

描述信息

(+)-car-3-ene is a car-3-ene (3,7,7-trimethylbicyclo[4.1.0]hept-3-ene) that has S configuration at position 1 and R configuration at position 6. It is an enantiomer of a (-)-car-3-ene.
(+)-3-Carene is a natural product found in Molopospermum peloponnesiacum, Kippistia suaedifolia, and other organisms with data available.

同义名列表

57 个代谢物同义名

(+)-3-delta-Carene, primary pharmaceutical reference standard; Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-, (1S,6R)-; Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S,6R)-; Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S)-; (1R,6S)-4,7,7-trimethylbicyclo[4.1.0]hept-3-ene; (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene; (1S)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene; (1S)-3,7,7-Trimethylbicyclo(4.1.0)hept-3-ene; Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-; (+)-3-Carene 1000 microg/mL in Isopropanol; (+)-3-Carene, analytical standard; 3,7,7-trimethyl bicyclohept-3-ene; 4,7,7-Trimethyl-3-norcarene; BQOFWKZOCNGFEC-BDAKNGLRSA-N; 3-carene, (S)-(cis)-isomer; (1S)-(+)-3-Carene, 99\\%; 1alpha,6alpha-car-3-ene; 3-Carene, (1S,6R)-(+)-; 3-carene, (R)-isomer; (1S,6R)-(+)-3-carene; (+)-Delta(3)-carene; (+)-.delta.3-Carene; (1S)-(+)-3-Carene; .DELTA.-caR-3-ene; (+)-delta3-Carene; (1S,6R)-3-Carene; (+)-alpha-carene; .delta. 3-carene; (S)-(+)-3-Carene; .delta.-3-Carene; 3-.delta.-Carene; delta(3)-carene; UNII-XBL40A7IA6; delta-3-carene; (+)-D-3-Carene; 3-Carene, (+)-; delta3-carene; (+)-car-3-ene; (+)-3-Carene; Isodiprene; XBL40A7IA6; 3-carene; CHEBI:7; Carene; 3,7,7-trimethyl-bicyclo[4.1.0]hept-3-ene; 3,7,7-Trimethylbicyclo[4.1.0]-3-heptene; 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene; (+-)-delta3-Carene; Delta-car-3-ene; 3-delta-Carene; (+-)-3-Carene; alpha-Carene; Car-3-ene; 3-Carene; (+)-3-Carene; Car-3-ene; (+)-3-Carene



数据库引用编号

26 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

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)

286 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。

亚细胞结构定位 关联基因列表
Cytoplasm 9 AHR, ALOX5, ARNT, CAT, CYP2B6, CYP2C19, CYP2D6, PMP2, TYR
Peripheral membrane protein 4 ACHE, ALOX5, CYP1B1, CYP2B6
Endoplasmic reticulum membrane 7 CYP1A2, CYP1B1, CYP2B6, CYP2C19, CYP2D6, RAC2, SPP1
Nucleus 6 ACHE, AHR, ARNT, CS, OGDH, PMP2
cytosol 5 AHR, ALOX5, CAT, PMP2, RAC2
mitochondrial membrane 1 OGDH
nuclear body 1 ARNT
nucleoplasm 4 AHR, ALOX5, ARNT, ATP2B1
RNA polymerase II transcription regulator complex 1 ARNT
Cell membrane 3 ACHE, ATP2B1, SPP1
lamellipodium 1 RAC2
Multi-pass membrane protein 2 ATP2B1, SPP1
Synapse 2 ACHE, ATP2B1
cell surface 1 ACHE
glutamatergic synapse 1 ATP2B1
Golgi apparatus 3 ACHE, ATRN, SPP1
lysosomal membrane 1 GAA
neuromuscular junction 1 ACHE
presynaptic membrane 1 ATP2B1
Cytoplasm, cytosol 1 ALOX5
Lysosome 2 GAA, TYR
plasma membrane 8 ACHE, ATP2B1, ATRN, BCHE, CYP2C19, GAA, RAC2, SPP1
synaptic vesicle membrane 1 ATP2B1
Membrane 7 ACHE, ATP2B1, CAT, CS, CYP1B1, CYP2D6, GAA
basolateral plasma membrane 1 ATP2B1
extracellular exosome 8 ATP2B1, ATRN, CAT, CS, GAA, PMP2, RAC2, SPP1
Lysosome membrane 1 GAA
endoplasmic reticulum 1 CYP2D6
extracellular space 5 ACHE, ALOX5, ATRN, BCHE, SPP1
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 4 ACHE, ALOX5, SPP1, TYR
mitochondrion 5 CAT, CS, CYP1B1, CYP2D6, OGDH
protein-containing complex 2 AHR, CAT
intracellular membrane-bounded organelle 9 ATP2B1, CAT, CYP1A2, CYP1B1, CYP2B6, CYP2C19, CYP2D6, GAA, TYR
Microsome membrane 4 CYP1A2, CYP1B1, CYP2B6, CYP2D6
Single-pass type I membrane protein 2 ATRN, TYR
Secreted 4 ACHE, BCHE, GAA, SPP1
extracellular region 6 ACHE, ALOX5, BCHE, CAT, GAA, SPP1
Single-pass membrane protein 1 CYP2D6
mitochondrial outer membrane 1 RAC2
[Isoform 2]: Secreted 1 ATRN
Mitochondrion matrix 1 CS
mitochondrial matrix 3 CAT, CS, OGDH
Extracellular side 1 ACHE
transcription regulator complex 2 AHR, ARNT
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
Nucleus membrane 1 ALOX5
nuclear membrane 1 ALOX5
Melanosome membrane 1 TYR
Golgi-associated vesicle 1 TYR
Cytoplasm, perinuclear region 1 ALOX5
focal adhesion 2 CAT, RAC2
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
lateral plasma membrane 1 ATP2B1
chromatin 2 AHR, ARNT
cell projection 2 ATP2B1, SPP1
phagocytic vesicle membrane 1 RAC2
blood microparticle 1 BCHE
Basolateral cell membrane 1 ATP2B1
Lipid-anchor, GPI-anchor 1 ACHE
[Isoform 3]: Secreted 1 ATRN
nuclear envelope 2 ALOX5, RAC2
Nucleus envelope 1 ALOX5
aryl hydrocarbon receptor complex 2 AHR, ARNT
tertiary granule membrane 1 GAA
Melanosome 1 TYR
Presynaptic cell membrane 1 ATP2B1
side of membrane 1 ACHE
myelin sheath 1 PMP2
ficolin-1-rich granule lumen 2 ALOX5, CAT
secretory granule lumen 2 ALOX5, CAT
endoplasmic reticulum lumen 2 BCHE, SPP1
nuclear matrix 1 ALOX5
azurophil granule membrane 1 GAA
immunological synapse 1 ATP2B1
Nucleus matrix 1 ALOX5
nuclear envelope lumen 2 ALOX5, BCHE
oxoglutarate dehydrogenase complex 1 OGDH
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
[Isoform 1]: Cell membrane 1 ATRN
catalase complex 1 CAT
NADPH oxidase complex 1 RAC2
Nucleus intermembrane space 1 ALOX5
autolysosome lumen 1 GAA
photoreceptor ribbon synapse 1 ATP2B1
[Isoform H]: Cell membrane 1 ACHE
nuclear aryl hydrocarbon receptor complex 2 AHR, ARNT
cytosolic aryl hydrocarbon receptor complex 1 AHR


文献列表

  • Edmund J Norris, Jeffrey R Bloomquist. Fir (Abies balsamea) (Pinales: Pinaceae) needle essential oil enhances the knockdown activity of select insecticides. Journal of medical entomology. 2023 Nov; 60(6):1350-1356. doi: 10.1093/jme/tjad101. [PMID: 37963276]
  • 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]
  • Renxuan Zou, Baoyu Li, Wengui Duan, Guishan Lin, Yucheng Cui. Synthesis of 3-carene-derived nanocellulose/1,3,4-thiadiazole-amide complexes with antifungal activity for plant protection. Pest management science. 2022 Aug; 78(8):3277-3286. doi: 10.1002/ps.6952. [PMID: 35484724]
  • Lina Pan, Weifang Xiang, Zeyang Sun, Yixin Yang, Jiayi Han, Yonghui Wang, Chuncai Yan, Min Li. CcOBP2 plays a crucial role in 3-carene olfactory response of the parasitoid wasp Chouioia cunea. Insect biochemistry and molecular biology. 2020 02; 117(?):103286. doi: 10.1016/j.ibmb.2019.103286. [PMID: 31760134]
  • Mei Wang, Amar G Chittiboyina, Jon F Parcher, Zulfiqar Ali, Paul Ford, Jianping Zhao, Bharathi Avula, Yan-Hong Wang, Ikhlas A Khan. Piper nigrum Oil - Determination of Selected Terpenes for Quality Evaluation. Planta medica. 2019 Feb; 85(3):185-194. doi: 10.1055/a-0782-0548. [PMID: 30440078]
  • Emanuele Pallozzi, Ilaria Lusini, Lucia Cherubini, Ramilla A Hajiaghayeva, Paolo Ciccioli, Carlo Calfapietra. Differences between a deciduous and a conifer tree species in gaseous and particulate emissions from biomass burning. Environmental pollution (Barking, Essex : 1987). 2018 Mar; 234(?):457-467. doi: 10.1016/j.envpol.2017.11.080. [PMID: 29207297]
  • Gabriel Garcia, Adrien Garcia, Marc Gibernau, Ange Bighelli, Félix Tomi. Chemical compositions of essential oils of five introduced conifers in Corsica. Natural product research. 2017 Jul; 31(14):1697-1703. doi: 10.1080/14786419.2017.1285299. [PMID: 28278672]
  • Mary L Reid, Jagdeep K Sekhon, Lanielle M LaFramboise. Toxicity of Monoterpene Structure, Diversity and Concentration to Mountain Pine Beetles, Dendroctonus ponderosae: Beetle Traits Matter More. Journal of chemical ecology. 2017 Apr; 43(4):351-361. doi: 10.1007/s10886-017-0824-1. [PMID: 28258318]
  • Lunzhao Yi, Naiping Dong, Shao Liu, Zhibiao Yi, Yi Zhang. Chemical features of Pericarpium Citri Reticulatae and Pericarpium Citri Reticulatae Viride revealed by GC-MS metabolomics analysis. Food chemistry. 2015 Nov; 186(?):192-9. doi: 10.1016/j.foodchem.2014.07.067. [PMID: 25976810]
  • Dušan Materić, Matteo Lanza, Philipp Sulzer, Jens Herbig, Dan Bruhn, Claire Turner, Nigel Mason, Vincent Gauci. Monoterpene separation by coupling proton transfer reaction time-of-flight mass spectrometry with fastGC. Analytical and bioanalytical chemistry. 2015 Oct; 407(25):7757-63. doi: 10.1007/s00216-015-8942-5. [PMID: 26253230]
  • Yukari Sunohara, Yohei Baba, Shigeru Matsuyama, Kaori Fujimura, Hiroshi Matsumoto. Screening and identification of phytotoxic volatile compounds in medicinal plants and characterizations of a selected compound, eucarvone. Protoplasma. 2015 Jul; 252(4):1047-59. doi: 10.1007/s00709-014-0739-4. [PMID: 25534256]
  • Rodrigo Alonso, Federico J Berli, Rubén Bottini, Patricia Piccoli. Acclimation mechanisms elicited by sprayed abscisic acid, solar UV-B and water deficit in leaf tissues of field-grown grapevines. Plant physiology and biochemistry : PPB. 2015 Jun; 91(?):56-60. doi: 10.1016/j.plaphy.2015.03.011. [PMID: 25885355]
  • Lukas Schmidt, Vladimir N Belov, Thomas Göen. Human metabolism of Δ3-carene and renal elimination of Δ3-caren-10-carboxylic acid (chaminic acid) after oral administration. Archives of toxicology. 2015 Mar; 89(3):381-92. doi: 10.1007/s00204-014-1251-5. [PMID: 24819613]
  • Le T Huong, Do N Dai, Tran D Thang, Tran T Bach, Isiaka A Ogunwande. Volatile constituents of Amomum maximum Roxb and Amomum microcarpum C. F. Liang & D. Fang: two Zingiberaceae grown in Vietnam. Natural product research. 2015; 29(15):1469-72. doi: 10.1080/14786419.2014.1003064. [PMID: 25600992]
  • Peter Harley, Allyson Eller, Alex Guenther, Russell K Monson. Observations and models of emissions of volatile terpenoid compounds from needles of ponderosa pine trees growing in situ: control by light, temperature and stomatal conductance. Oecologia. 2014 Sep; 176(1):35-55. doi: 10.1007/s00442-014-3008-5. [PMID: 25015120]
  • Daniele Fraternale, Guido Flamini, Donata Ricci. Essential oil composition and antimicrobial activity of Angelica archangelica L. (Apiaceae) roots. Journal of medicinal food. 2014 Sep; 17(9):1043-7. doi: 10.1089/jmf.2013.0012. [PMID: 24788027]
  • Samy A Selim, Mohammed E Adam, Sherif M Hassan, Abdulrhman R Albalawi. Chemical composition, antimicrobial and antibiofilm activity of the essential oil and methanol extract of the Mediterranean cypress (Cupressus sempervirens L.). BMC complementary and alternative medicine. 2014 Jun; 14(?):179. doi: 10.1186/1472-6882-14-179. [PMID: 24890383]
  • Do N Dai, Tran D Thang, Isiaka A Ogunwande. Chemical composition of essential oils from the leaves and stem barks of Vietnamese species of Polyalthia harmandii, Polyalthia jucunda and Polyalthia thorelii. Natural product research. 2014; 28(8):555-62. doi: 10.1080/14786419.2014.886209. [PMID: 24520907]
  • Lukas Schmidt, Vladimir N Belov, Thomas Göen. Sensitive monitoring of monoterpene metabolites in human urine using two-step derivatisation and positive chemical ionisation-tandem mass spectrometry. Analytica chimica acta. 2013 Sep; 793(?):26-36. doi: 10.1016/j.aca.2013.07.046. [PMID: 23953203]
  • P A Olounladé, E V B Azando, M S Hounzangbé-Adoté, T B Tam Ha, E Leroy, C Moulis, N Fabre, J F Magnaval, H Hoste, A Valentin. In vitro anthelmintic activity of the essential oils of Zanthoxylum zanthoxyloides and Newbouldia laevis against Strongyloides ratti. Parasitology research. 2012 Apr; 110(4):1427-33. doi: 10.1007/s00436-011-2645-4. [PMID: 21960378]
  • Danilo Aros, Veronica Gonzalez, Rudolf K Allemann, Carsten T Müller, Carlo Rosati, Hilary J Rogers. Volatile emissions of scented Alstroemeria genotypes are dominated by terpenes, and a myrcene synthase gene is highly expressed in scented Alstroemeria flowers. Journal of experimental botany. 2012 Apr; 63(7):2739-52. doi: 10.1093/jxb/err456. [PMID: 22268153]
  • Emmanuel Buschiazzo, Carol Ritland, Jörg Bohlmann, Kermit Ritland. Slow but not low: genomic comparisons reveal slower evolutionary rate and higher dN/dS in conifers compared to angiosperms. BMC evolutionary biology. 2012 Jan; 12(?):8. doi: 10.1186/1471-2148-12-8. [PMID: 22264329]
  • Marcela Dvorakova, Irena Valterova, David Saman, Tomas Vanek. Biotransformation of (1S)-2-carene and (1S)-3-carene by Picea abies suspension culture. Molecules (Basel, Switzerland). 2011 Dec; 16(12):10541-55. doi: 10.3390/molecules161210541. [PMID: 22183881]
  • A Vazquez-Luna, F Rivera-Cabrera, L J Perez-Flores, R Diaz-Sobac. Effect of rootstock on mango fruit susceptibility to infestation by Anastrepha obliqua. Journal of economic entomology. 2011 Dec; 104(6):1991-8. doi: 10.1603/ec11223. [PMID: 22299362]
  • Axel Schmidt, Raimund Nagel, Trygve Krekling, Erik Christiansen, Jonathan Gershenzon, Paal Krokene. Induction of isoprenyl diphosphate synthases, plant hormones and defense signalling genes correlates with traumatic resin duct formation in Norway spruce (Picea abies). Plant molecular biology. 2011 Dec; 77(6):577-90. doi: 10.1007/s11103-011-9832-7. [PMID: 22002747]
  • Marie Danielsson, Karl Lundén, Malin Elfstrand, Jiang Hu, Tao Zhao, Jenny Arnerup, Katarina Ihrmark, Gunilla Swedjemark, Anna-Karin Borg-Karlson, Jan Stenlid. Chemical and transcriptional responses of Norway spruce genotypes with different susceptibility to Heterobasidion spp. infection. BMC plant biology. 2011 Nov; 11(?):154. doi: 10.1186/1471-2229-11-154. [PMID: 22067529]
  • M B Gholivand, M Rahimi-Nasrabadi, E Mehraban, M Niasari, H Batooli. Determination of the chemical composition and in vitro antioxidant activities of essential oil and methanol extracts of Echinophora platyloba DC. Natural product research. 2011 Oct; 25(17):1585-95. doi: 10.1080/14786419.2010.490915. [PMID: 21644173]
  • Smail Aazza, Badiâ Lyoussi, Maria G Miguel. Antioxidant and antiacetylcholinesterase activities of some commercial essential oils and their major compounds. Molecules (Basel, Switzerland). 2011 Sep; 16(9):7672-90. doi: 10.3390/molecules16097672. [PMID: 21900869]
  • Aaron S Adams, Celia K Boone, Jörg Bohlmann, Kenneth F Raffa. Responses of bark beetle-associated bacteria to host monoterpenes and their relationship to insect life histories. Journal of chemical ecology. 2011 Aug; 37(8):808-17. doi: 10.1007/s10886-011-9992-6. [PMID: 21710365]
  • Gábor Markó, Ildikó Novák, Jeno Bernáth, Vilmos Altbäcker. Both gas chromatography and an electronic nose reflect chemical polymorphism of juniper shrubs browsed or avoided by sheep. Journal of chemical ecology. 2011 Jul; 37(7):705-13. doi: 10.1007/s10886-011-9974-8. [PMID: 21626295]
  • Christopher I Keeling, Sabrina Weisshaar, Steven G Ralph, Sharon Jancsik, Britta Hamberger, Harpreet K Dullat, Jörg Bohlmann. Transcriptome mining, functional characterization, and phylogeny of a large terpene synthase gene family in spruce (Picea spp.). BMC plant biology. 2011 Mar; 11(?):43. doi: 10.1186/1471-2229-11-43. [PMID: 21385377]
  • Aihong Zhao, Xiuwei Yang, Xinbao Yang, Wenquan Wang, Haiyan Tao. [GC-MS analysis of essential oil from root of Angelica dahurica cv. Qibaizhi]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Mar; 36(5):603-7. doi: 10.4268/cjcmm20110519. [PMID: 21657081]
  • Dawn E Hall, Jeanne A Robert, Christopher I Keeling, Dominik Domanski, Alfonso Lara Quesada, Sharon Jancsik, Michael A Kuzyk, Britta Hamberger, Christoph H Borchers, Jörg Bohlmann. An integrated genomic, proteomic and biochemical analysis of (+)-3-carene biosynthesis in Sitka spruce (Picea sitchensis) genotypes that are resistant or susceptible to white pine weevil. The Plant journal : for cell and molecular biology. 2011 Mar; 65(6):936-48. doi: 10.1111/j.1365-313x.2010.04478.x. [PMID: 21323772]
  • Sébastien Verne, Barry Jaquish, Rick White, Carol Ritland, Kermit Ritland. Global transcriptome analysis of constitutive resistance to the white pine weevil in spruce. Genome biology and evolution. 2011; 3(?):851-67. doi: 10.1093/gbe/evr069. [PMID: 21852250]
  • Zhudong Liu, Bo Wang, Bingbing Xu, Jianghua Sun. Monoterpene variation mediated attack preference evolution of the bark beetle Dendroctonus valens. PloS one. 2011; 6(7):e22005. doi: 10.1371/journal.pone.0022005. [PMID: 21811555]
  • Xavier Font, Adriana Artola, Antoni Sánchez. Detection, composition and treatment of volatile organic compounds from waste treatment plants. Sensors (Basel, Switzerland). 2011; 11(4):4043-59. doi: 10.3390/s110404043. [PMID: 22163835]
  • Carmine Summo, Francesco Caponio, Francesco Tricarico, Antonella Pasqualone, Tommaso Gomes. Evolution of the volatile compounds of ripened sausages as a function of both storage time and composition of packaging atmosphere. Meat science. 2010 Nov; 86(3):839-44. doi: 10.1016/j.meatsci.2010.07.006. [PMID: 20678868]
  • Luis Sampedro, Xoaquín Moreira, Joan Llusia, Josep Peñuelas, Rafael Zas. Genetics, phosphorus availability, and herbivore-derived induction as sources of phenotypic variation of leaf volatile terpenes in a pine species. Journal of experimental botany. 2010 Oct; 61(15):4437-47. doi: 10.1093/jxb/erq246. [PMID: 20952630]
  • Tao Zhao, Paal Krokene, Niklas Björklund, Bo Långström, Halvor Solheim, Erik Christiansen, Anna-Karin Borg-Karlson. The influence of Ceratocystis polonica inoculation and methyl jasmonate application on terpene chemistry of Norway spruce, Picea abies. Phytochemistry. 2010 Aug; 71(11-12):1332-41. doi: 10.1016/j.phytochem.2010.05.017. [PMID: 20557909]
  • Min Lu, Michael J Wingfield, Nancy E Gillette, Sylvia R Mori, Jiang-Hua Sun. Complex interactions among host pines and fungi vectored by an invasive bark beetle. The New phytologist. 2010 Aug; 187(3):859-66. doi: 10.1111/j.1469-8137.2010.03316.x. [PMID: 20546136]
  • Carolina I Paris, Joan Llusia, Josep Peñuelas. Changes in monoterpene emission rates of Quercus ilex infested by aphids tended by native or invasive Lasius ant species. Journal of chemical ecology. 2010 Jul; 36(7):689-98. doi: 10.1007/s10886-010-9815-1. [PMID: 20549328]
  • Tjeerd A L Snoeren, Iris F Kappers, Colette Broekgaarden, Roland Mumm, Marcel Dicke, Harro J Bouwmeester. Natural variation in herbivore-induced volatiles in Arabidopsis thaliana. Journal of experimental botany. 2010 Jun; 61(11):3041-56. doi: 10.1093/jxb/erq127. [PMID: 20488836]
  • Hui-Jing Gu, Sen-Sung Cheng, Chun-Ya Lin, Chin-Gi Huang, Wei-June Chen, Shang-Tzen Chang. Repellency of essential oils of Cryptomeria japonica (Pinaceae) against adults of the mosquitoes Aedes aegypti and Aedes albopictus (Diptera:Culicidae). Journal of agricultural and food chemistry. 2009 Dec; 57(23):11127-33. doi: 10.1021/jf9024486. [PMID: 19902948]
  • Katherine G Zulak, Dustin N Lippert, Michael A Kuzyk, Dominik Domanski, Tina Chou, Christoph H Borchers, Jörg Bohlmann. Targeted proteomics using selected reaction monitoring reveals the induction of specific terpene synthases in a multi-level study of methyl jasmonate-treated Norway spruce (Picea abies). The Plant journal : for cell and molecular biology. 2009 Dec; 60(6):1015-30. doi: 10.1111/j.1365-313x.2009.04020.x. [PMID: 19754519]
  • Björn Hamberger, Dawn Hall, Mack Yuen, Claire Oddy, Britta Hamberger, Christopher I Keeling, Carol Ritland, Kermit Ritland, Jörg Bohlmann. Targeted isolation, sequence assembly and characterization of two white spruce (Picea glauca) BAC clones for terpenoid synthase and cytochrome P450 genes involved in conifer defence reveal insights into a conifer genome. BMC plant biology. 2009 Aug; 9(?):106. doi: 10.1186/1471-2229-9-106. [PMID: 19656416]
  • L Nzira, M Per, F Peter, B Claus. Lippia javanica (Burm F) Spreng: its general constituents and bioactivity on mosquitoes. Tropical biomedicine. 2009 Apr; 26(1):85-91. doi: ". [PMID: 19696732]
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