(±)-3-Methyl-1-pentanol (BioDeep_00000021613)
human metabolite
代谢物信息卡片
化学式: C6H14O (102.10445940000001)
中文名称: 3-甲基-1-戊醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCC(C)CCO
InChI: InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3
描述信息
(±)-3-Methyl-1-pentanol, also known as 3-ethylbutanol or 3-methyl-(+/-)-1-pentanol, belongs to the class of organic compounds known as primary alcohols. Primary alcohols are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl). (±)-3-Methyl-1-pentanol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Thus, (±)-3-Methyl-1-pentanol is considered to be a fatty alcohol lipid molecule. (±)-3-Methyl-1-pentanol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. (±)-3-Methyl-1-pentanol is a cocoa, cognac, and fruity tasting compound. (±)-3-Methyl-1-pentanol has been detected, but not quantified, in cornmints.
(±)-3-methyl-1-pentanol, also known as 3-ethylbutanol or 3-methyl-(.+/-.)-1-pentanol, is a member of the class of compounds known as primary alcohols. Primary alcohols are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl). Thus, (±)-3-methyl-1-pentanol is considered to be a fatty alcohol lipid molecule (±)-3-methyl-1-pentanol is soluble (in water) and an extremely weak acidic compound (based on its pKa). (±)-3-methyl-1-pentanol can be found primarily in feces. Within the cell, (±)-3-methyl-1-pentanol is primarily located in the cytoplasm. It can also be found in the extracellular space.
同义名列表
数据库引用编号
10 个数据库交叉引用编号
- ChEBI: CHEBI:87381
- PubChem: 11508
- HMDB: HMDB0033676
- KNApSAcK: C00035792
- foodb: FDB008173
- chemspider: 11024
- CAS: 343268-11-1
- CAS: 20281-83-8
- CAS: 589-35-5
- PMhub: MS000067259
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)
6 个相关的物种来源信息
- 265783 - Artemisia capillaris: 10.1016/J.JPBA.2004.01.025
- 9606 - Homo sapiens: -
- 73200 - Pelargonium graveolens: 10.1002/HLCA.19840670504
- 4081 - Solanum lycopersicum: 10.1021/JF00014A016
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 569774 - 金线莲: -
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
- Miklós Tóth, István Szarukán, Béla Dorogi, Attila Gulyás, Pál Nagy, Zoltán Rozgonyi. Male and female noctuid moths attracted to synthetic lures in Europe.
Journal of chemical ecology.
2010 Jun; 36(6):592-8. doi:
10.1007/s10886-010-9789-z
. [PMID: 20449640] - Laura R Jarboe, Xueli Zhang, Xuan Wang, Jonathan C Moore, K T Shanmugam, Lonnie O Ingram. Metabolic engineering for production of biorenewable fuels and chemicals: contributions of synthetic biology.
Journal of biomedicine & biotechnology.
2010; 2010(?):761042. doi:
10.1155/2010/761042
. [PMID: 20414363] - H J Doller, J D Connor, D R Lock, R S Sloviter, B H Dvorchik, E S Vesell. Levodopa pharmacokinetics. Alterations after benserazide, a decarboxylase inhibitor.
Drug metabolism and disposition: the biological fate of chemicals.
1978 Mar; 6(2):164-8. doi:
NULL
. [PMID: 26532]