(+)-Longifolene (BioDeep_00000327975)

Main id: BioDeep_00000004306

 

PANOMIX_OTCML-2023


代谢物信息卡片


(+)-Longifolene

化学式: C15H24 (204.18779039999998)
中文名称: 长叶烯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C=C1C2(C)CCCC(C)(C)C13CCC2C3
InChI: InChI=1S/C15H24/c1-10-11-6-7-12-13(11)14(2,3)8-5-9-15(10,12)4/h11-13H,1,5-9H2,2-4H3

描述信息

(+)-Longifolene is a sesquiterpenoid and a metabolite in rabbits. (+)-Longifolen is converted to primary, secondary or tertiary alcohols in rabbits, among which the primary alcohol is predominant[1].
(+)-Longifolene is a sesquiterpenoid and a metabolite in rabbits. (+)-Longifolen is converted to primary, secondary or tertiary alcohols in rabbits, among which the primary alcohol is predominant[1].
(+)-Longifolene is a sesquiterpenoid and a metabolite in rabbits. (+)-Longifolen is converted to primary, secondary or tertiary alcohols in rabbits, among which the primary alcohol is predominant[1].

同义名列表

2 个代谢物同义名

(+)-Longifolene; LONGIFOLENE



数据库引用编号

10 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)

28 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

  • Furong Xia, Jingping Du, Kai Wang, Lu Liu, Limin Ba, Huan Liu, Yanhui Liu. Application of Multiple Strategies To Debottleneck the Biosynthesis of Longifolene by Engineered Saccharomyces cerevisiae. Journal of agricultural and food chemistry. 2022 Sep; 70(36):11336-11343. doi: 10.1021/acs.jafc.2c04405. [PMID: 36047715]
  • Madhuri Grover, Tapan Behl, Tarun Virmani, Mohit Sanduja, Hafiz A Makeen, Mohammed Albratty, Hassan A Alhazmi, Abdulkarim M Meraya, Simona Gabriela Bungau. Exploration of Cytotoxic Potential of Longifolene/Junipene Isolated from Chrysopogon zizanioides. Molecules (Basel, Switzerland). 2022 Sep; 27(18):. doi: 10.3390/molecules27185764. [PMID: 36144491]
  • Yujin Cao, Rubing Zhang, Wei Liu, Guang Zhao, Wei Niu, Jiantao Guo, Mo Xian, Huizhou Liu. Manipulation of the precursor supply for high-level production of longifolene by metabolically engineered Escherichia coli. Scientific reports. 2019 01; 9(1):95. doi: 10.1038/s41598-018-36495-w. [PMID: 30643175]
  • 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]
  • Miao Wang, Dongyu Gu, Haoquan Li, Qi Wang, Jie Kang, Tingting Chu, Hong Guo, Yi Yang, Jing Tian. Rapid prediction and identification of lipase inhibitors in volatile oil from Pinus massoniana L. needles. Phytochemistry. 2017 Sep; 141(?):114-120. doi: 10.1016/j.phytochem.2017.06.002. [PMID: 28609696]
  • N Karami, A Karimi, A Aliahmadi, F Mirzajan, H Rezadoost, A Ghassempour, F Fallah. Identification of bacteria using volatile organic compounds. Cellular and molecular biology (Noisy-le-Grand, France). 2017 Feb; 63(2):112-121. doi: 10.14715/cmb/2017.63.2.18. [PMID: 28364792]
  • Ilan Botnick, Wentao Xue, Einat Bar, Mwafaq Ibdah, Amnon Schwartz, Daniel M Joel, Efraim Lev, Aaron Fait, Efraim Lewinsohn. Distribution of primary and specialized metabolites in Nigella sativa seeds, a spice with vast traditional and historical uses. Molecules (Basel, Switzerland). 2012 Aug; 17(9):10159-77. doi: 10.3390/molecules170910159. [PMID: 22922285]
  • Lin Yang, Lirui Qiao, Dan Xie, Jungui Dai, Shunxing Guo. [Sesquiterpenes and monoterpene from Aquilaria sinensis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 Jul; 37(13):1973-6. doi: . [PMID: 23019881]
  • Rafal Szmigielski, Marek Cieslak, Krzysztof J Rudziński, Barbara Maciejewska. Identification of volatiles from Pinus silvestris attractive for Monochamus galloprovincialis using a SPME-GC/MS platform. Environmental science and pollution research international. 2011 Aug; 19(7):2860-9. doi: 10.1007/s11356-012-0792-5. [PMID: 22322293]
  • Cheryl Lans, Nancy Turner. Organic parasite control for poultry and rabbits in British Columbia, Canada. Journal of ethnobiology and ethnomedicine. 2011 Jul; 7(?):21. doi: 10.1186/1746-4269-7-21. [PMID: 21756341]
  • 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]
  • 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]
  • Amir Reza Jassbi, Simin Zamanizadehnajari, Ian Thomas Baldwin. Phytotoxic volatiles in the roots and shoots of Artemisia tridentata as detected by headspace solid-phase microextraction and gas chromatographic-mass spectrometry analysis. Journal of chemical ecology. 2010 Dec; 36(12):1398-407. doi: 10.1007/s10886-010-9885-0. [PMID: 21086024]
  • Frank Bedon, Claude Bomal, Sébastien Caron, Caroline Levasseur, Brian Boyle, Shawn D Mansfield, Axel Schmidt, Jonathan Gershenzon, Jacqueline Grima-Pettenati, Armand Séguin, John MacKay. Subgroup 4 R2R3-MYBs in conifer trees: gene family expansion and contribution to the isoprenoid- and flavonoid-oriented responses. Journal of experimental botany. 2010 Sep; 61(14):3847-64. doi: 10.1093/jxb/erq196. [PMID: 20732878]
  • Andréa Y Gordien, Alexander I Gray, Scott G Franzblau, Véronique Seidel. Antimycobacterial terpenoids from Juniperus communis L. (Cuppressaceae). Journal of ethnopharmacology. 2009 Dec; 126(3):500-5. doi: 10.1016/j.jep.2009.09.007. [PMID: 19755141]
  • Diana Köpke, Roland Schröder, Hanna M Fischer, Jonathan Gershenzon, Monika Hilker, Axel Schmidt. Does egg deposition by herbivorous pine sawflies affect transcription of sesquiterpene synthases in pine?. Planta. 2008 Aug; 228(3):427-38. doi: 10.1007/s00425-008-0747-8. [PMID: 18493792]
  • Li Lin Zhao, Wei Wei, Le Kang, Jiang Hua Sun. Chemotaxis of the pinewood nematode, Bursaphelenchus xylophilus, to volatiles associated with host pine, Pinus massoniana, and its vector Monochamus alternatus. Journal of chemical ecology. 2007 Jun; 33(6):1207-16. doi: 10.1007/s10886-007-9289-y. [PMID: 17447123]
  • José Luis Torres-Estrada, R Amanda Meza-Alvarez, Juan Cibrián-Tovar, Mario H Rodríguez-López, Juan I Arredondo-Jiménez, Leopoldo Cruz-López, Julio C Rojas-Leon. Vegetation-derived cues for the selection of oviposition substrates by Anopheles albimanus under laboratory conditions. Journal of the American Mosquito Control Association. 2005 Dec; 21(4):344-9. doi: 10.2987/8756-971x(2006)21[344:vcftso]2.0.co;2. [PMID: 16506557]
  • Shan-Shan Yao, Wen-Fei Guo, Yi Lu, Yuan-Xun Jiang. Flavor characteristics of lapsang souchong and smoked lapsang souchong, a special Chinese black tea with pine smoking process. Journal of agricultural and food chemistry. 2005 Nov; 53(22):8688-93. doi: 10.1021/jf058059i. [PMID: 16248572]
  • Julieta Rubio, José S Calderón, Angélica Flores, Clementina Castroa, Carlos L Céspedes. Trypanocidal activity of oleoresin and terpenoids isolated from Pinus oocarpa. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2005 Sep; 60(9-10):711-6. doi: 10.1515/znc-2005-9-1009. [PMID: 16320613]
  • Dezene P W Huber, Ryan N Philippe, Lufiani L Madilao, Rona N Sturrock, Jörg Bohlmann. Changes in anatomy and terpene chemistry in roots of Douglas-fir seedlings following treatment with methyl jasmonate. Tree physiology. 2005 Aug; 25(8):1075-83. doi: 10.1093/treephys/25.8.1075. [PMID: 15929938]
  • Johannes Panten, Heinz-Jürgen Bertram, Horst Surburg. New woody and ambery notes from cedarwood and turpentine oil. Chemistry & biodiversity. 2004 Dec; 1(12):1936-48. doi: 10.1002/cbdv.200490148. [PMID: 17191830]
  • P B Pedersen, J D Miller. The fungal metabolite culmorin and related compounds. Natural toxins. 1999; 7(6):305-9. doi: 10.1002/1522-7189(199911/12)7:6<305::aid-nt72>3.0.co;2-g. [PMID: 11122521]