3-Hexanol (BioDeep_00000021967)
human metabolite Endogenous natural product
代谢物信息卡片
化学式: C6H14O (102.1045)
中文名称: 3-己醇
谱图信息:
最多检出来源 not specific(not specific) 0%
分子结构信息
SMILES: CCCC(CC)O
InChI: InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3
描述信息
3-Hexanol, also known as fema 3351 or 3-hexyl alcohol, belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R) (R,R=alkyl, aryl). 3-Hexanol is an alcoholic, ether, and medicinal tasting compound. 3-Hexanol is found, on average, in the highest concentration within safflowers. 3-Hexanol has also been detected, but not quantified, in several different foods, such as green bell peppers, orange bell peppers, pepper (c. annuum), red bell peppers, and yellow bell peppers.
3-Hexanol occurs naturally in the flavor and aroma of plants such as pineapple and is used as a food additive to add flavor. 3-Hexanol is found in many foods, some of which are pepper (c. annuum), red bell pepper, orange bell pepper, and green bell pepper.
同义名列表
6 个代谢物同义名
Ethyl propyl carbinol; 3-Hexyl alcohol; hexan-3-ol; 3-HEXANOL; FEMA 3351; 3-Hexanol
数据库引用编号
11 个数据库交叉引用编号
- ChEBI: CHEBI:88653
- PubChem: 12178
- HMDB: HMDB0031493
- ChEMBL: CHEMBL46678
- Wikipedia: 3-hexanol
- KNApSAcK: C00055659
- foodb: FDB008073
- chemspider: 11678
- CAS: 623-37-0
- PMhub: MS000074968
- LOTUS: LTS0232984
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)
22 个相关的物种来源信息
- 260129 - Acca: LTS0232984
- 260130 - Acca sellowiana: 10.1016/S0031-9422(00)97781-1
- 260130 - Acca sellowiana: LTS0232984
- 25641 - Aloe: LTS0232984
- 1080010 - Aloe africana: 10.1021/JF010179C
- 1080010 - Aloe africana: LTS0232984
- 51383 - Asphodelaceae: LTS0232984
- 2706 - Citrus: LTS0232984
- 558547 - Citrus deliciosa: 10.1590/S0100-40422002000700009
- 85571 - Citrus reticulata: 10.1590/S0100-40422002000700009
- 85571 - Citrus reticulata: LTS0232984
- 2759 - Eukaryota: LTS0232984
- 58987 - Freesia: LTS0232984
- 9606 - Homo sapiens: -
- 26339 - Iridaceae: LTS0232984
- 4447 - Liliopsida: LTS0232984
- 3398 - Magnoliopsida: LTS0232984
- 3931 - Myrtaceae: LTS0232984
- 23513 - Rutaceae: LTS0232984
- 35493 - Streptophyta: LTS0232984
- 58023 - Tracheophyta: LTS0232984
- 33090 - Viridiplantae: LTS0232984
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 |
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文献列表
- Sebastian Peter, Matthias Kinne, Xiaoshi Wang, René Ullrich, Gernot Kayser, John T Groves, Martin Hofrichter. Selective hydroxylation of alkanes by an extracellular fungal peroxygenase.
The FEBS journal.
2011 Oct; 278(19):3667-75. doi:
10.1111/j.1742-4658.2011.08285.x
. [PMID: 21812933] - Virginie Gosset, Nicolas Harmel, Cornelia Göbel, Frédéric Francis, Eric Haubruge, Jean-Paul Wathelet, Patrick du Jardin, Ivo Feussner, Marie-Laure Fauconnier. Attacks by a piercing-sucking insect (Myzus persicae Sultzer) or a chewing insect (Leptinotarsa decemlineata Say) on potato plants (Solanum tuberosum L.) induce differential changes in volatile compound release and oxylipin synthesis.
Journal of experimental botany.
2009; 60(4):1231-40. doi:
10.1093/jxb/erp015
. [PMID: 19221142] - Hui-Lin Yu, Yong-Jun Zhang, Wen-Liang Pan, Yu-Yuan Guo, Xi-Wu Gao. [Identification of volatiles from field cotton plant under different induction treatments].
Ying yong sheng tai xue bao = The journal of applied ecology.
2007 Apr; 18(4):859-64. doi:
"
. [PMID: 17615885] - M Sano. Subcellular localizations of guanylate cyclase and 3',5'-cyclic nucleotide phosphodiesterase in sea urchin sperm.
Biochimica et biophysica acta.
1976 Apr; 428(2):525-31. doi:
10.1016/0304-4165(76)90061-1
. [PMID: 6049]