Isopentyl isopentanoate (BioDeep_00000014684)
Secondary id: BioDeep_00001873910
human metabolite Endogenous
代谢物信息卡片
化学式: C10H20O2 (172.14632200000003)
中文名称: 异戊酸异戊酯
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C)CCOC(=O)CC(C)C
InChI: InChI=1S/C10H20O2/c1-8(2)5-6-12-10(11)7-9(3)4/h8-9H,5-7H2,1-4H3
描述信息
Isopentyl isopentanoate, also known as iso-amyl isovalerate or 3-methylbutyl isovalerate, belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Isopentyl isopentanoate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.
Constituent of banana fruit and tomatoes and alcoholic beverages e.g. cognac, cider. Flavouring agent. Isopentyl isopentanoate is found in many foods, some of which are spearmint, orange mint, garden tomato, and alcoholic beverages.
同义名列表
24 个代谢物同义名
Butanoic acid, 3-methyl-, 3-methylbutyl ester; 3-Methylbutanoic acid 3-methylbutyl ester; Isovaleric acid, isopentyl ester; 3-methylbutyl 3-methylbutanoate; Isopentyl alcohol, isovalerate; 3-Methylbutyl 3-methylbutyrate; Isopentyl 3-methylbutanoate; Isopentyl isopentanoic acid; Isopentyl 3-methylbutyrate; 3-Methylbutyl isovalerate; Isoamyl 3-methylbutanoate; Isoamyl 3-methylbutyrate; Isopentyl isopentanoate; Isoamyl isovalerianate; Isoamyl isopentanoate; Isopentyl isovalerate; iso-Amyl isovalerate; ISOAMYL ISOVALERATE; Isoamyl valerianate; Apple essence; Solusterol; Apple oil; FEMA 2085; WE 10:0
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:31727
- KEGG: C12289
- PubChem: 12613
- HMDB: HMDB0030029
- Metlin: METLIN69415
- ChEMBL: CHEMBL3189076
- LipidMAPS: LMFA07010919
- foodb: FDB001327
- chemspider: 12093
- CAS: 659-70-1
- PMhub: MS000182433
- PubChem: 14433
- NIKKAJI: J2.103B
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)
30 个相关的物种来源信息
- 698833 - Elsholtzia fruticosa: 10.1055/S-2006-961490
- 1711142 - Eucalyptus angulosa: 10.1002/FFJ.2730090305
- 1711173 - Eucalyptus behriana: 10.1002/FFJ.2730100605
- 1341233 - Eucalyptus bridgesiana: 10.1080/10412905.1991.9697984
- 34316 - Eucalyptus camaldulensis: 10.1080/10412905.1991.9697921
- 1711216 - Eucalyptus ceratocorys: 10.1002/FFJ.2730090305
- 1711242 - Eucalyptus cuprea: 10.1002/FFJ.2730100605
- 1711273 - Eucalyptus dolichorhyncha: 10.1002/FFJ.2730090305
- 1226037 - Eucalyptus fasciculosa: 10.1002/FFJ.2730100605
- 1711306 - Eucalyptus forrestiana: 10.1002/FFJ.2730090305
- 1711342 - Eucalyptus incrassata: 10.1002/FFJ.2730090305
- 1226038 - Eucalyptus intertexta: 10.1002/FFJ.2730100605
- 87673 - Eucalyptus lansdowneana: 10.1002/FFJ.2730100605
- 34318 - Eucalyptus leucoxylon: 10.1002/FFJ.2730100605
- 1234623 - Eucalyptus melanophloia: 10.1002/FFJ.2730100605
- 87674 - Eucalyptus nitens: 10.1016/S0031-9422(00)94539-4
- 1711436 - Eucalyptus ochrophloia: 10.1002/FFJ.2730100605
- 2660570 - Eucalyptus odorata: 10.1002/FFJ.2730100605
- 183848 - Eucalyptus populnea: 10.1002/FFJ.2730100605
- 795992 - Eucalyptus porosa: 10.1002/FFJ.2730100605
- 1711536 - Eucalyptus sparsa: 10.1002/FFJ.2730100605
- 87686 - Eucalyptus stoatei: 10.1002/FFJ.2730090305
- 1711566 - Eucalyptus tetraptera: 10.1002/FFJ.2730090305
- 1711585 - Eucalyptus viridis: 10.1002/FFJ.2730100605
- 380073 - Heracleum dissectum: 10.1021/NP50041A034
- 193516 - Hippophae rhamnoides: 10.1002/PCA.2413
- 9606 - Homo sapiens: -
- 65561 - Hypericum perforatum: 10.1080/14786411003792165
- 190902 - Mentha aquatica: 10.1271/NOGEIKAGAKU1924.67.1417
- 59170 - Valeriana jatamansi: 10.1002/CBDV.201100059
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
- Mohammad M Hudaib, Khaled A Tawaha, Mohammad K Mohammad, Areej M Assaf, Ala Y Issa, Feras Q Alali, Talal A Aburjai, Yasser K Bustanji. Xanthine oxidase inhibitory activity of the methanolic extracts of selected Jordanian medicinal plants.
Pharmacognosy magazine.
2011 Oct; 7(28):320-4. doi:
10.4103/0973-1296.90413
. [PMID: 22262935] - Mohamed Sellami, Imen Aissa, Fakher Frikha, Youssef Gargouri, Nabil Miled. Immobilized Rhizopus oryzae lipase catalyzed synthesis of palm stearin and cetyl alcohol wax esters: optimization by response surface methodology.
BMC biotechnology.
2011 Jun; 11(?):68. doi:
10.1186/1472-6750-11-68
. [PMID: 21682865] - Ian A Southwell. 25 years of natural product R&D with New South Wales agriculture.
Molecules (Basel, Switzerland).
2005 Oct; 10(10):1232-41. doi:
10.3390/10101232
. [PMID: 18007515]