Bornyl acetate (BioDeep_00000228005)

Main id: BioDeep_00000395765

 

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate

化学式: C12H20O2 (196.14632200000003)
中文名称: (-)-冰片醇乙酸酯, 乙酸冰片酯, （1S，2R，4S）-（-）-乙酸硼酸酯, （-）-乙酸硼酸酯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=O)OC1CC2CCC1(C)C2(C)C
InChI: InChI=1S/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/m0/s1

描述信息

Bornyl acetate, also known as bornyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Bornyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Bornyl acetate is a camphor, cedar, and herbal tasting compound and can be found in a number of food items such as nutmeg, rosemary, spearmint, and sunflower, which makes bornyl acetate a potential biomarker for the consumption of these food products.
(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].
Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

同义名列表

22 个代谢物同义名

(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate; (1S-endo)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate; (1S)-1,7,7-Trimethylbicyclo[2.2.1]-2-heptanol acetate; 1S-endo-Bornyl acetate; (-)-Bornyl acetic acid; endo-bornyl acetate; (-)-Borneol acetate; Bornyl acetic ester; levo-Bornyl acetate; (-)-Bornyl acetate; Bornyl acetic acid; (±)-Bornyl acetate; (+)-Bornyl acetate; dl-Bornyl acetate; Bornyl ethanoate; L-Bornyl acetate; Borneyl acetate; Bornyl acetate; L-(-)-Bornyl acetate; (1S,2R,4S)-(-)-Bornyl acetate; (1S,2R,4S)-(-)-Bornyl acetate; (-)-Bornyl acetate



数据库引用编号

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789 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。

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