(E)-carveol (BioDeep_00000638362)

Main id: BioDeep_00000004185

 


代谢物信息卡片


(1S-trans)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol

化学式: C10H16O (152.12010859999998)
中文名称: (1R,5S)-rel-香芹醇, 香芹醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CCC(CC1O)C(=C)C
InChI: InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10+/m1/s1

描述信息

同义名列表

3 个代谢物同义名

(1S-trans)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol; (-)-trans-Carveol; (E)-carveol



数据库引用编号

12 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)

55 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

  • S Jana, G S Shekhawat. Anethum graveolens: An Indian traditional medicinal herb and spice. Pharmacognosy reviews. 2010 Jul; 4(8):179-84. doi: 10.4103/0973-7847.70915. [PMID: 22228959]
  • Peng Wang, Chui Hua Kong, Chao Xian Zhang. Chemical composition and antimicrobial activity of the essential oil from Ambrosia trifida L. Molecules (Basel, Switzerland). 2006 Jul; 11(7):549-55. doi: 10.3390/11070549. [PMID: 17971726]
  • Kerry L Ringer, Edward M Davis, Rodney Croteau. Monoterpene metabolism. Cloning, expression, and characterization of (-)-isopiperitenol/(-)-carveol dehydrogenase of peppermint and spearmint. Plant physiology. 2005 Mar; 137(3):863-72. doi: 10.1104/pp.104.053298. [PMID: 15734920]
  • Vijai K Agnihotri, Rajendra K Thappa, Baleshwar Meena, Bal K Kapahi, Rajendra K Saxena, Ghulam N Qazi, Shri G Agarwal. Essential oil composition of aerial parts of Angelica glauca growing wild in North-West Himalaya (India). Phytochemistry. 2004 Aug; 65(16):2411-3. doi: 10.1016/j.phytochem.2004.07.004. [PMID: 15381015]
  • Katumi Umano, Yukio Hagi, Takayuki Shibamoto. Volatile chemicals identified in extracts from newly hybrid citrus, dekopon (Shiranuhi mandarin Suppl. J.). Journal of agricultural and food chemistry. 2002 Sep; 50(19):5355-9. doi: 10.1021/jf0203951. [PMID: 12207474]
  • Matthias Wüst, Rodney B Croteau. Hydroxylation of specifically deuterated limonene enantiomers by cytochrome p450 limonene-6-hydroxylase reveals the mechanism of multiple product formation. Biochemistry. 2002 Feb; 41(6):1820-7. doi: 10.1021/bi011717h. [PMID: 11827526]
  • M Wüst, D B Little, M Schalk, R Croteau. Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from mint (Mentha) species: evidence for catalysis within sterically constrained active sites. Archives of biochemistry and biophysics. 2001 Mar; 387(1):125-36. doi: 10.1006/abbi.2000.2248. [PMID: 11368174]
  • E W Watt, J Wiley, G F Fletcher. Effect of dietary control and exercise training on daily food intake and serum lipids in postmyocardial infarction patients. The American journal of clinical nutrition. 1976 Aug; 29(8):900-4. doi: 10.1093/ajcn/29.8.900. [PMID: 181978]