Valencene (BioDeep_00000872588)

Main id: BioDeep_00000000969

 

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


NAPHTHALENE, 1,2,3,5,6,7,8,8A-OCTAHYDRO-1,8A-DIMETHYL-7-(1-METHYLETHENYL)-, (1R-(1.ALPHA.,7.BETA.,8A.ALPHA.))-

化学式: C15H24 (204.1878)
中文名称: (+)-瓦伦亚烯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C=C(C)C1CCC2=CCCC(C)C2(C)C1
InChI: InChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h7,12-13H,1,5-6,8-10H2,2-4H3

描述信息

(+)-valencene is a carbobicyclic compound and sesquiterpene that is 1,2,3,4,4a,5,6,7-octahydronaphthalene which is substituted a prop-1-en-2-yl group at position 3 and by methyl groups at positions 4a and 5 (the 3R,4aS,5R- diastereoisomer). It is a sesquiterpene, a carbobicyclic compound and a polycyclic olefin.
Valencene is a natural product found in Xylopia sericea, Helichrysum odoratissimum, and other organisms with data available.
Constituent of orange oil. Valencene is found in many foods, some of which are citrus, common oregano, rosemary, and sweet orange.
Valencene is a sesquiterpene isolated from Cyperus rotundus, possesses antiallergic, antimelanogenesis, anti-infammatory, and antioxidant activitivies. Valencene inhibits the exaggerated expression of Th2 chemokines and proinflammatory chemokines through blockade of the NF-κB pathway. Valencene is used to flavor foods and drinks[1][2][3].

同义名列表

29 个代谢物同义名

NAPHTHALENE, 1,2,3,5,6,7,8,8A-OCTAHYDRO-1,8A-DIMETHYL-7-(1-METHYLETHENYL)-, (1R-(1.ALPHA.,7.BETA.,8A.ALPHA.))-; Naphthalene, 1,2,3,5,6,7,8,8A-octahydro-1,8A-dimethyl-7-(1-methylethenyl)-, (1R-(1alpha,7beta,8aalpha))-; 1,2,3,5,6,7,8,8a-Octahydro-1,8A-dimethyl-7-(1-methylethenyl)naphthalene, (1R-(1alpha,7beta,8aalpha))-; (1R-(1alpha,7beta,8alpha))-1,2,3,5,6,7,8,8a-Octahydro-1,8a-dimethyl-7-(1-methylvinyl)naphthalene; Naphthalene, 1,2,3,5,6,7,8,8a-octahydro-1,8a-dimethyl-7-(1-methylethenyl)-, (1R,7R,8aS)-; (3R,4aS,5R)-4a,5-dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene; (3R,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene; (3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene; 4alpha,10alpha-Dimethyl-6beta-isopropyl-.DELTA.1,9-octalin; 4alpha,10alpha-Dimethyl-6beta-isopropyl-delta1,9-octalin; 4.beta.H,5.alpha.-Eremophila-1(10),11-diene; 4Betah,5alpha-eremophila-1(10),11-diene; ent-7betaH-eremophila-10(1),11-diene; (+)-Valencene, analytical standard; (+)-Valencene, technical, >=70\\%; QEBNYNLSCGVZOH-NFAWXSAZSA-N; Valencene, natural, >=65\\%; (+)-Valencene, tech grade; Valencene (natural); (A+/-)-valencene; VALENCENE [FHFI]; VALENCENE [INCI]; UNII-96H21P91IG; (+)-Valencene; Tox21_302397; 96H21P91IG; Valencene; Valencen; (+)-Valencene



数据库引用编号

18 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)

268 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 7 ALB, FDPS, HMGB1, MAPK8, MSRA, NQO1, PTGS2
Peripheral membrane protein 3 CYP1B1, HMGB1, PTGS2
Endoplasmic reticulum membrane 5 CYP1B1, FDFT1, HMOX1, HTN1, PTGS2
Nucleus 7 ALB, CYC1, GABPA, HMGB1, HMOX1, MAPK8, NQO1
cytosol 6 ALB, FDPS, HMOX1, MAPK8, MSRA, NQO1
dendrite 1 NQO1
centrosome 1 ALB
nucleoplasm 6 FDPS, GABPA, HMGB1, HMOX1, MAPK8, MSRA
Cell membrane 4 HMGB1, ORAI1, TNF, TRPV1
Lipid-anchor 1 MSRA
Cytoplasmic side 1 HMOX1
Multi-pass membrane protein 3 FDFT1, ORAI1, TRPV1
Synapse 3 ACAN, MAPK8, NQO1
cell surface 2 HMGB1, TNF
glutamatergic synapse 1 ACAN
Golgi apparatus 2 ALB, ATRN
mitochondrial inner membrane 1 CYC1
neuronal cell body 3 NQO1, TNF, TRPV1
Cytoplasm, cytosol 1 NQO1
endosome 1 HMGB1
plasma membrane 7 ATRN, HMGB1, IGHE, MSRA, ORAI1, TNF, TRPV1
Membrane 9 CYC1, CYP1B1, FDFT1, FDPS, HMOX1, MSRA, NQO1, ORAI1, TRPV1
axon 1 MAPK8
basolateral plasma membrane 1 ORAI1
caveola 1 PTGS2
extracellular exosome 3 ALB, ATRN, MSRA
endoplasmic reticulum 6 ALB, FDFT1, HMGB1, HMOX1, HTN1, PTGS2
extracellular space 7 ACAN, ALB, ATRN, HMGB1, HMOX1, IGHE, TNF
lysosomal lumen 1 ACAN
perinuclear region of cytoplasm 1 HMOX1
mitochondrion 4 CYC1, CYP1B1, HTN1, MSRA
protein-containing complex 2 ALB, PTGS2
intracellular membrane-bounded organelle 2 CYP1B1, MSRA
Microsome membrane 2 CYP1B1, PTGS2
Single-pass type I membrane protein 2 ATRN, IGHE
Secreted 2 ALB, HMGB1
extracellular region 7 ACAN, ALB, HMGB1, HTN1, IGHE, PROK2, TNF
Single-pass membrane protein 1 CYC1
mitochondrial outer membrane 1 HMOX1
[Isoform 2]: Secreted 1 ATRN
mitochondrial matrix 1 FDPS
Extracellular side 1 HMGB1
anchoring junction 1 ALB
external side of plasma membrane 2 TNF, TRPV1
Secreted, extracellular space, extracellular matrix 1 ACAN
actin cytoskeleton 1 MSRA
midbody 1 MSRA
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
postsynaptic membrane 1 TRPV1
Mitochondrion inner membrane 1 CYC1
Membrane raft 2 ORAI1, TNF
GABA-ergic synapse 2 ACAN, TRPV1
Peroxisome 1 FDPS
basement membrane 1 ACAN
collagen-containing extracellular matrix 1 ACAN
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Postsynaptic cell membrane 1 TRPV1
Cell projection, neuron projection 1 TRPV1
neuron projection 1 PTGS2
ciliary basal body 1 ALB
chromatin 1 GABPA
IgE immunoglobulin complex 1 IGHE
phagocytic cup 1 TNF
Chromosome 1 HMGB1
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
Basolateral cell membrane 1 ORAI1
[Isoform 2]: Cell membrane 1 IGHE
[Isoform 3]: Secreted 1 ATRN
plasma membrane raft 1 ORAI1
ficolin-1-rich granule lumen 1 HMGB1
secretory granule lumen 1 HMGB1
Golgi lumen 1 ACAN
endoplasmic reticulum lumen 2 ALB, PTGS2
transcription repressor complex 1 HMGB1
platelet alpha granule lumen 1 ALB
perineuronal net 1 ACAN
Single-pass type IV membrane protein 1 HMOX1
respiratory chain complex III 1 CYC1
calcium channel complex 1 ORAI1
endoplasmic reticulum-Golgi intermediate compartment 1 HMGB1
basal dendrite 1 MAPK8
[Isoform 1]: Cell membrane 1 ATRN
condensed chromosome 1 HMGB1
Cell projection, dendritic spine membrane 1 TRPV1
dendritic spine membrane 1 TRPV1
[Isoform 3]: Cell membrane 1 IGHE
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
alphav-beta3 integrin-HMGB1 complex 1 HMGB1
perisynaptic extracellular matrix 1 ACAN
ciliary transition fiber 1 ALB
[Isoform Alpha]: Cell membrane 1 ORAI1
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
[Isoform beta]: Cell membrane 1 ORAI1


文献列表

  • Lingling Ma, Tao Wu, Peiling Liu, Dongying Chen, Shengliang Cai, Hefeng Chen, Jingtao Zhou, Chaoyi Zhu, Shuang Li. Green Production of a High-value Mosquito Insecticide of Nootkatone from Seaweed Hydrolysates. Journal of agricultural and food chemistry. 2023 Dec; 71(48):18919-18927. doi: 10.1021/acs.jafc.3c06708. [PMID: 37991146]
  • Xiaomin Deng, Ziling Ye, Jingyu Duan, Fangfang Chen, Yao Zhi, Man Huang, Minjian Huang, Weijia Cheng, Yujie Dou, Zhaolin Kuang, Yanglei Huang, Guangkai Bian, Zixin Deng, Tiangang Liu, Li Lu. Complete pathway elucidation and heterologous reconstitution of (+)-nootkatone biosynthesis from Alpinia oxyphylla. The New phytologist. 2023 Nov; ?(?):. doi: 10.1111/nph.19375. [PMID: 37933426]
  • Chunyang Cao, Haiyan Zhang, Xuan Cao, Sijia Kong, Beiwei Zhu, Xinping Lin, Yongjin J Zhou. Construction and Optimization of Nonclassical Isoprenoid Biosynthetic Pathways in Yeast Peroxisomes for (+)-Valencene Production. Journal of agricultural and food chemistry. 2023 Jul; ?(?):. doi: 10.1021/acs.jafc.3c02932. [PMID: 37437260]
  • Fapetu Kemi Busayo, Jin-Ling Yang, Xu-Po Ding, Ya-Li Wang, Cui-Juan Gai, Fei Wu, Hao-Fu Dai, Wen-Li Mei, Hui-Qin Chen. Identification of volatile compounds and their bioactivities from unpolar fraction of Alpinia oxyphylla Miq. and mining key genes of nootkatone biosynthesis. Natural product research. 2023 Jun; ?(?):1-6. doi: 10.1080/14786419.2023.2220063. [PMID: 37278024]
  • Lindaiane B R Dantas, Isabel S Alcântara, Cícero Pedro S Júnior, Maria Rayane C de Oliveira, Anita O B P B Martins, Ticiano M Dantas, Jaime Ribeiro-Filho, Henrique Douglas M Coutinho, Fabíolla R S Passos, Lucindo J Quintans-Júnior, Jackson Roberto G S Almeida, Natália Cruz-Martins, Bonglee Kim, Irwin Rose Alencar de Menezes. In vivo and in silico anti-inflammatory properties of the sesquiterpene valencene. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Sep; 153(?):113478. doi: 10.1016/j.biopha.2022.113478. [PMID: 36076580]
  • Yuqin Gou, Fangyuan Zhang, Yueli Tang, Chunxue Jiang, Ge Bai, He Xie, Min Chen, Zhihua Liao. Engineering Nootkatone Biosynthesis in Artemisia annua. ACS synthetic biology. 2021 05; 10(5):957-963. doi: 10.1021/acssynbio.1c00016. [PMID: 33973783]
  • Haipeng Zhang, Huan Wen, Jiajing Chen, Zhaoxin Peng, Meiyan Shi, Mengjun Chen, Ziyu Yuan, Yuan Liu, Hongyan Zhang, Juan Xu. Volatile Compounds in Fruit Peels as Novel Biomarkers for the Identification of Four Citrus Species. Molecules (Basel, Switzerland). 2019 Dec; 24(24):. doi: 10.3390/molecules24244550. [PMID: 31842378]
  • Qibin Yu, Ming Huang, Hongge Jia, Yuan Yu, Anne Plotto, Elizabeth A Baldwin, Jinhe Bai, Nian Wang, Frederick G Gmitter. Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene. BMC plant biology. 2019 Mar; 19(1):101. doi: 10.1186/s12870-019-1701-6. [PMID: 30866831]
  • Ana E T Alcoba, Daiana C de Melo, Priscila M de Andrade, Herbert J Dias, Mariana C Pagotti, Lizandra G Magalhães, Walnir G F Júnior, Antônio E M Crotti, Mayker L D Miranda. Chemical composition and in vitro antileishmanial and cytotoxic activities of the essential oils of Ocotea dispersa (Nees) Mez and Ocotea odorifera (Vell) Rohwer (Lauraceae). Natural product research. 2018 Dec; 32(23):2865-2868. doi: 10.1080/14786419.2017.1385007. [PMID: 29022353]
  • Rungarun Tisgratog, Chutipong Sukkanon, John P Grieco, Unchalee Sanguanpong, Kamlesh R Chauhan, Joel R Coats, Theeraphap Chareonviriyaphap. Evaluation of the Constituents of Vetiver Oil Against Anopheles minimus (Diptera: Culicidae), a Malaria Vector in Thailand. Journal of medical entomology. 2018 01; 55(1):193-199. doi: 10.1093/jme/tjx188. [PMID: 29029183]
  • Cassandra Federman, Christopher Ma, Debabrata Biswas. Major components of orange oil inhibit Staphylococcus aureus growth and biofilm formation, and alter its virulence factors. Journal of medical microbiology. 2016 Jul; 65(7):688-695. doi: 10.1099/jmm.0.000286. [PMID: 27259704]
  • Shu-Ling Shen, Xue-Ren Yin, Bo Zhang, Xiu-Lan Xie, Qian Jiang, Donald Grierson, Kun-Song Chen. CitAP2.10 activation of the terpene synthase CsTPS1 is associated with the synthesis of (+)-valencene in 'Newhall' orange. Journal of experimental botany. 2016 07; 67(14):4105-15. doi: 10.1093/jxb/erw189. [PMID: 27194737]
  • Katarina Cankar, Esmer Jongedijk, Martin Klompmaker, Timotej Majdic, Roland Mumm, Harro Bouwmeester, Dirk Bosch, Jules Beekwilder. (+)-Valencene production in Nicotiana benthamiana is increased by down-regulation of competing pathways. Biotechnology journal. 2015 Jan; 10(1):180-9. doi: 10.1002/biot.201400288. [PMID: 25159317]
  • Robin-Hagen Leonhardt, Ralf G Berger. Nootkatone. Advances in biochemical engineering/biotechnology. 2015; 148(?):391-404. doi: 10.1007/10_2014_279. [PMID: 25326849]
  • Kamala Jayanthi Pagadala Damodaram, Vivek Kempraj, Ravindra Mahadappa Aurade, Sowmya Bandhisara Rajasekhar, Ravindra Kothapalli Venkataramanappa, Bakthavatsalam Nandagopal, Abraham Verghese. Centuries of domestication has not impaired oviposition site-selection function in the silkmoth, Bombyx mori. Scientific reports. 2014 Dec; 4(?):7472. doi: 10.1038/srep07472. [PMID: 25503440]
  • Jonas Frohwitter, Sabine A E Heider, Petra Peters-Wendisch, Jules Beekwilder, Volker F Wendisch. Production of the sesquiterpene (+)-valencene by metabolically engineered Corynebacterium glutamicum. Journal of biotechnology. 2014 Dec; 191(?):205-13. doi: 10.1016/j.jbiotec.2014.05.032. [PMID: 24910970]
  • Jules Beekwilder, Adèle van Houwelingen, Katarina Cankar, Aalt D J van Dijk, René M de Jong, Geert Stoopen, Harro Bouwmeester, Jihane Achkar, Theo Sonke, Dirk Bosch. Valencene synthase from the heartwood of Nootka cypress (Callitropsis nootkatensis) for biotechnological production of valencene. Plant biotechnology journal. 2014 Feb; 12(2):174-82. doi: 10.1111/pbi.12124. [PMID: 24112147]
  • Kehai Liu, Qiulin Chen, Yanjun Liu, Xiaoyan Zhou, Xichang Wang. Isolation and biological activities of decanal, linalool, valencene, and octanal from sweet orange oil. Journal of food science. 2012 Nov; 77(11):C1156-61. doi: 10.1111/j.1750-3841.2012.02924.x. [PMID: 23106968]
  • Selvaraju Kanagarajan, Saraladevi Muthusamy, Anna Gliszczyńska, Anneli Lundgren, Peter E Brodelius. Functional expression and characterization of sesquiterpene synthases from Artemisia annua L. using transient expression system in Nicotiana benthamiana. Plant cell reports. 2012 Jul; 31(7):1309-19. doi: 10.1007/s00299-012-1250-z. [PMID: 22565787]
  • 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]
  • Keqin Yu, Qiang Xu, Xinlei Da, Fei Guo, Yuduan Ding, Xiuxin Deng. Transcriptome changes during fruit development and ripening of sweet orange (Citrus sinensis). BMC genomics. 2012 Jan; 13(?):10. doi: 10.1186/1471-2164-13-10. [PMID: 22230690]
  • Trinh-Don Nguyen, Gillian MacNevin, Dae-Kyun Ro. De novo synthesis of high-value plant sesquiterpenoids in yeast. Methods in enzymology. 2012; 517(?):261-78. doi: 10.1016/b978-0-12-404634-4.00013-9. [PMID: 23084943]
  • Mokhtar Guerfel, Mohamed Ben Mansour, Youssef Ouni, Flamini Guido, Dalenda Boujnah, Mokhtar Zarrouk. Triacylglycerols composition and volatile compounds of virgin olive oil from Chemlali cultivar: comparison among different planting densities. TheScientificWorldJournal. 2012; 2012(?):354019. doi: 10.1100/2012/354019. [PMID: 22629139]
  • Petra M Bleeker, Eleni A Spyropoulou, Paul J Diergaarde, Hanne Volpin, Michiel T J De Both, Philipp Zerbe, Joerg Bohlmann, Vasiliki Falara, Yuki Matsuba, Eran Pichersky, Michel A Haring, Robert C Schuurink. RNA-seq discovery, functional characterization, and comparison of sesquiterpene synthases from Solanum lycopersicum and Solanum habrochaites trichomes. Plant molecular biology. 2011 Nov; 77(4-5):323-36. doi: 10.1007/s11103-011-9813-x. [PMID: 21818683]
  • Konstantin Tsoyi, Hwa Jin Jang, Young Soo Lee, Young Min Kim, Hye Jung Kim, Han Geuk Seo, Jae Heun Lee, Jong Hwan Kwak, Dong-Ung Lee, Ki Churl Chang. (+)-Nootkatone and (+)-valencene from rhizomes of Cyperus rotundus increase survival rates in septic mice due to heme oxygenase-1 induction. Journal of ethnopharmacology. 2011 Oct; 137(3):1311-7. doi: 10.1016/j.jep.2011.07.062. [PMID: 21843620]
  • Moran Farhi, Elena Marhevka, Tania Masci, Evgeniya Marcos, Yoram Eyal, Mariana Ovadis, Hagai Abeliovich, Alexander Vainstein. Harnessing yeast subcellular compartments for the production of plant terpenoids. Metabolic engineering. 2011 Sep; 13(5):474-81. doi: 10.1016/j.ymben.2011.05.001. [PMID: 21601648]
  • Abdul Ahad, Mohammed Aqil, Kanchan Kohli, Yasmin Sultana, Mohd Mujeeb, Asgar Ali. Role of novel terpenes in transcutaneous permeation of valsartan: effectiveness and mechanism of action. Drug development and industrial pharmacy. 2011 May; 37(5):583-96. doi: 10.3109/03639045.2010.532219. [PMID: 21469947]
  • Jeong Ho Jin, Dong-Ung Lee, Yeong Shik Kim, Hyun Pyo Kim. Anti-allergic activity of sesquiterpenes from the rhizomes of Cyperus rotundus. Archives of pharmacal research. 2011 Feb; 34(2):223-8. doi: 10.1007/s12272-011-0207-z. [PMID: 21380805]
  • Katarina Cankar, Adèle van Houwelingen, Dirk Bosch, Theo Sonke, Harro Bouwmeester, Jules Beekwilder. A chicory cytochrome P450 mono-oxygenase CYP71AV8 for the oxidation of (+)-valencene. FEBS letters. 2011 Jan; 585(1):178-82. doi: 10.1016/j.febslet.2010.11.040. [PMID: 21115006]
  • Qing Liu, Mohammad Majdi, Katarina Cankar, Miriam Goedbloed, Tatsiana Charnikhova, Francel W A Verstappen, Ric C H de Vos, Jules Beekwilder, Sander van der Krol, Harro J Bouwmeester. Reconstitution of the costunolide biosynthetic pathway in yeast and Nicotiana benthamiana. PloS one. 2011; 6(8):e23255. doi: 10.1371/journal.pone.0023255. [PMID: 21858047]
  • Alírica I Suárez, Marly Oropeza, Luis Vásquez, Stephen Tillett, Reinaldo S Compagnone. Chemical composition of the essential oil of Croton gossypiifolius from Venezuela. Natural product communications. 2011 Jan; 6(1):97-9. doi: . [PMID: 21366055]
  • Gabino Ríos, Miguel A Naranjo, María-Jesús Rodrigo, Enriqueta Alós, Lorenzo Zacarías, Manuel Cercós, Manuel Talón. Identification of a GCC transcription factor responding to fruit colour change events in citrus through the transcriptomic analyses of two mutants. BMC plant biology. 2010 Dec; 10(?):276. doi: 10.1186/1471-2229-10-276. [PMID: 21159189]
  • Mengsu Huang, Christian Abel, Reza Sohrabi, Jana Petri, Ina Haupt, John Cosimano, Jonathan Gershenzon, Dorothea Tholl. Variation of herbivore-induced volatile terpenes among Arabidopsis ecotypes depends on allelic differences and subcellular targeting of two terpene synthases, TPS02 and TPS03. Plant physiology. 2010 Jul; 153(3):1293-310. doi: 10.1104/pp.110.154864. [PMID: 20463089]
  • Ilizandra A Fernandes, Maria Carolina Esmelindro, Marcos L Corazza, Elton Franceschi, Helen Treichel, Debora de Oliveira, Caren D Frizzo, J Vladimir Oliveira. Catalytic oxidation of concentrated orange oil phase by synthetic metallic complexes biomimetic to MMO enzyme. Journal of the science of food and agriculture. 2010 Jul; 90(9):1460-6. doi: 10.1002/jsfa.3964. [PMID: 20549797]
  • Lisieux de Santana Julião, Humberto R Bizzo, Andressa M Souza, Maria Cristina S Lourenço, Pedro Eduardo A Silva, Eliana S Tavares, Luca Rastrelli, Suzana Guimarães Leitão. Essential oils from two Lantana species with antimycobacterial activity. Natural product communications. 2009 Dec; 4(12):1733-6. doi: . [PMID: 20120116]
  • T K Praveen, S Dharmaraj, Jitendra Bajaj, S P Dhanabal, S Manimaran, M J Nanjan, Rema Razdan. Hepatoprotective activity of petroleum ether, diethyl ether, and methanol extract of Scoparia dulcis L. against CCl4-induced acute liver injury in mice. Indian journal of pharmacology. 2009 Jun; 41(3):110-4. doi: 10.4103/0253-7613.55206. [PMID: 20442817]
  • Ramón E Robles-Zepeda, Edmundo Lozoya-Gloria, Mercedes G López, María L Villarreal, Enrique Ramírez-Chávez, Jorge Molina-Torres. Montanoa tomentosa glandular trichomes containing kaurenoic acids chemical profile and distribution. Fitoterapia. 2009 Jan; 80(1):12-7. doi: 10.1016/j.fitote.2008.09.002. [PMID: 18824221]
  • Mohammad A Asadollahi, Jérôme Maury, Kasper Møller, Kristian Fog Nielsen, Michel Schalk, Anthony Clark, Jens Nielsen. Production of plant sesquiterpenes in Saccharomyces cerevisiae: effect of ERG9 repression on sesquiterpene biosynthesis. Biotechnology and bioengineering. 2008 Feb; 99(3):666-77. doi: 10.1002/bit.21581. [PMID: 17705244]
  • Gen-ichiro Arimura, Stefan Garms, Massimo Maffei, Simone Bossi, Birgit Schulze, Margit Leitner, Axel Mithöfer, Wilhelm Boland. Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling. Planta. 2008 Jan; 227(2):453-64. doi: 10.1007/s00425-007-0631-y. [PMID: 17924138]
  • Manuel Talon, Fred G Gmitter. Citrus genomics. International journal of plant genomics. 2008; 2008(?):528361. doi: 10.1155/2008/528361. [PMID: 18509486]
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