(+)-Neomenthol (BioDeep_00000014728)

Main id: BioDeep_00000397415

 

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


(1S,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexan-1-ol

化学式: C10H20O (156.1514)
中文名称: (1Alpha,2Alpha,5β)-(+-)-5-甲基, (+)-新薄荷醇, DL-薄荷醇, l-薄荷醇, (+/-)-新薄荷醇, （+）-新薄荷醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O
InChI: InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10+/m1/s1

描述信息

Constituent of Japanese peppermint oil. Flavouring ingredient. (+)-Neomenthol is found in many foods, some of which are yellow bell pepper, broccoli, spearmint, and sweet orange.
(+)-Neomenthol is found in cabbage. (+)-Neomenthol is a constituent of Japanese peppermint oil. (+)-Neomenthol is a flavouring ingredient
(+)-Neomenthol is a potent miticide. (+)-Neomenthol shows acaricidal activitie with LD50 values of 0.32, 0.256 μg/mL for Dermatophagoides farinae and Dermatophagoides pteronyssinus, respectively[1].
(+)-Neomenthol is a potent miticide. (+)-Neomenthol shows acaricidal activitie with LD50 values of 0.32, 0.256 μg/mL for Dermatophagoides farinae and Dermatophagoides pteronyssinus, respectively[1].
DL-Menthol is a relative configuration of (-)-Menthol. DL-Menthol relates to the activation of GABAA receptor[1].
DL-Menthol is a relative configuration of (-)-Menthol. DL-Menthol relates to the activation of GABAA receptor[1].
DL-Menthol is a relative configuration of (-)-Menthol. DL-Menthol relates to the activation of GABAA receptor[1].

同义名列表

15 个代谢物同义名

(1S,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexan-1-ol; (1S,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexanol; (1S,2S,5R)-2-Isopropyl-5-methylcyclohexanol; (1S,2S,5R)-(+)-Neomenthol; dextro,laevo-neomenthol; (+)-neomenthol; D-Neomenthol; FEMA 2666; Menthol; Racementhol; DL-Menthol; (+)-Neomenthol; l-Menthol; Menthol; (+)-Neomenthol



数据库引用编号

25 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

代谢反应

4 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(2)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

46 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。

亚细胞结构定位 关联基因列表


文献列表

  • Ana M Fortes, Patricia Agudelo-Romero, Marta S Silva, Kashif Ali, Lisete Sousa, Federica Maltese, Young H Choi, Jerome Grimplet, José M Martinez-Zapater, Robert Verpoorte, Maria S Pais. Transcript and metabolite analysis in Trincadeira cultivar reveals novel information regarding the dynamics of grape ripening. BMC plant biology. 2011 Nov; 11(?):149. doi: 10.1186/1471-2229-11-149. [PMID: 22047180]
  • Anna-Margareta Rydén, Carolien Ruyter-Spira, Ralph Litjens, Shunji Takahashi, Wim Quax, Hiroyuki Osada, Harro Bouwmeester, Oliver Kayser. Molecular cloning and characterization of a broad substrate terpenoid oxidoreductase from Artemisia annua. Plant & cell physiology. 2010 Jul; 51(7):1219-28. doi: 10.1093/pcp/pcq073. [PMID: 20483909]
  • Jörg Ziegler, Peter J Facchini, René Geissler, Jürgen Schmidt, Christian Ammer, Robert Kramell, Susan Voigtländer, Andreas Gesell, Silke Pienkny, Wolfgang Brandt. Evolution of morphine biosynthesis in opium poppy. Phytochemistry. 2009 Oct; 70(15-16):1696-707. doi: 10.1016/j.phytochem.2009.07.006. [PMID: 19665152]
  • Marco Mucciarelli, Wanda Camusso, Massimo Maffei, Paola Panicco, Carlo Bicchi. Volatile terpenoids of endophyte-free and infected peppermint (Mentha piperita L.): chemical partitioning of a symbiosis. Microbial ecology. 2007 Nov; 54(4):685-96. doi: 10.1007/s00248-007-9227-0. [PMID: 17370029]
  • M Maffei, W Camusso, S Sacco. Effect of Mentha x piperita essential oil and monoterpenes on cucumber root membrane potential. Phytochemistry. 2001 Nov; 58(5):703-7. doi: 10.1016/s0031-9422(01)00313-2. [PMID: 11672734]