5EL0Y7P6LP (BioDeep_00000396400)

Main id: BioDeep_00000004944

 

PANOMIX_OTCML-2023


代谢物信息卡片


1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-, (S)-(-)-

化学式: C10H14O (150.1044594)
中文名称: (-)-紫苏醛, 紫苏醛
谱图信息: 最多检出来源 Viridiplantae(plant) 2.42%

分子结构信息

SMILES: C=C(C)[C@@H]1CC=C(C=O)CC1
InChI: InChI=1S/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,7,10H,1,4-6H2,2H3/t10-/m1/s1

描述信息

(-)-Perillaldehyde is a natural product found in Perilla frutescens var. crispa, Valeriana officinalis, and other organisms with data available.
See also: Paeonia lactiflora root (part of).
L-Perillaldehyde is a major component in the essential oil containing in Perillae Herba. Inhalation of L-Perillaldehyde shows antidepressant-like activity through the olfactory nervous function[1].
L-Perillaldehyde is a major component in the essential oil containing in Perillae Herba. Inhalation of L-Perillaldehyde shows antidepressant-like activity through the olfactory nervous function[1].

同义名列表

40 个代谢物同义名

1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-, (S)-(-)-; 1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-, (4S)-; 1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-, (S)-; 1-CYCLOHEXENE-1-CARBOXALDEHYDE, 4-ISOPROPENYL-, (S)-(-)-; (4S)-4-(1-Methylethenyl)-1-cyclohexene-1-carboxaldehyde; (4S)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carbaldehyde; (S)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carbaldehyde; (S)-4-Isopropenyl-1-cyclohexene-1-carboxaldehyde; 4-Isopropenyl-1-cyclohexene-1-carbaldehyde, (S)-; (S)-4-(prop-1-en-2-yl)cyclohex-1-enecarbaldehyde; (4S)-4-prop-1-en-2-ylcyclohexene-1-carbaldehyde; (4S)-4-Isopropenyl-1-cyclohexen-1-carbaldehyde; (S)-4-Isopropenyl-cyclohexene-1-carboxaldehyde; (S)-(-)-Perillaldehyde, technical grade, 92\\%; (4S)-4-isopropenylcyclohexene-1-carbaldehyde; (S)-(-)-Perillaldehyde, analytical standard; (S)-(-)-Perillaldehyde, >=92\\%; (4S)-p-Mentha-1,8-dien-7-al; RUMOYJJNUMEFDD-SNVBAGLBSA-N; PERILLALDEHYDE L-FORM [MI]; (S)-p-Mentha-1,8-dien-7-al; (S)-(-)-Perillic aldehyde; (-)-Perillaldehyde - 95\\%; (4S)-perillyl aldehyde; (S)-(-)-Perillaldehyde; (-)-perillyl aldehyde; PERILLALDEHYDE L-FORM; (-)-Perilla aldehyde; Perillaldehyde, (-)-; (-)-Perillaaldehyde; (?)-Perillaaldehyde; S(-)-Perillaldehyde; (-)-Perillaldehyde; (s)-perillaldehyde; 1-Perillaldehyde; L-Perillaldehyde; UNII-5EL0Y7P6LP; PERILLALDEHYDE; Tox21_300969; 5EL0Y7P6LP



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(1)

代谢反应

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(1)

  • perillyl aldehyde biosynthesis: (4S)-perillyl alcohol + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ (4S)-perillyl aldehyde + H2O + an oxidized [NADPH-hemoprotein reductase]

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

  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Mendel Friedman, Robert Buick, Christopher T Elliott. Antibacterial activities of naturally occurring compounds against antibiotic-resistant Bacillus cereus vegetative cells and spores, Escherichia coli, and Staphylococcus aureus. Journal of food protection. 2004 Aug; 67(8):1774-8. doi: 10.4315/0362-028x-67.8.1774. [PMID: 15330549]
  • Paul McGeady, Daniel L Wansley, David A Logan. Carvone and perillaldehyde interfere with the serum-induced formation of filamentous structures in Candida albicans at substantially lower concentrations than those causing significant inhibition of growth. Journal of natural products. 2002 Jul; 65(7):953-5. doi: 10.1021/np010621l. [PMID: 12141851]