Junipen (BioDeep_00000603357)

Main id: BioDeep_00000004306

 

PANOMIX_OTCML-2023


代谢物信息卡片


(+)-Longifolen;(1S,3aR,4S,8aS)-(+)-decahydro-4,8,8-trimethyl-9-methylene-1,4-methanoazulene;(1S,3aR,4S,8aS)-4,8,8-trimethyl-9-methylenedecahydro-1,4-methanoazulene

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: C1C[C@]2([H])C(=C)[C@@]3(C)CCCC(C)(C)[C@]2([H])[C@]31[H]
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/t11-,12-,13+,15-/m1/s1

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

9 个代谢物同义名

(+)-Longifolen;(1S,3aR,4S,8aS)-(+)-decahydro-4,8,8-trimethyl-9-methylene-1,4-methanoazulene;(1S,3aR,4S,8aS)-4,8,8-trimethyl-9-methylenedecahydro-1,4-methanoazulene; Longifolen;[1S-(1alpha,3abeta,4alpha,8abeta)]-decahydro-4,8,8-trimethyl-9-methylene-1,4-methanoazulene; (1S,3aR,4S,8aS)-4,8,8-trimethyl-9-methylidenedecahydro-1,4-methanoazulene; (+)-Longifolene; d-longifolene; kuromatsuene; Kuromatsuen; junipene; Junipen



数据库引用编号

7 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)

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]
  • Maria Graça Miguel, Maria Dulce Antunes. Is propolis safe as an alternative medicine?. Journal of pharmacy & bioallied sciences. 2011 Oct; 3(4):479-95. doi: 10.4103/0975-7406.90101. [PMID: 22219581]
  • 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]
  • Bharti Sapra, Subheet Jain, A K Tiwary. Percutaneous permeation enhancement by terpenes: mechanistic view. The AAPS journal. 2008; 10(1):120-32. doi: 10.1208/s12248-008-9012-0. [PMID: 18446512]
  • 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]
  • 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]
  • . . . . doi: . [PMID: 17192005]