2-Nonanol (BioDeep_00000024834)
human metabolite Endogenous Volatile Flavor Compounds natural product
代谢物信息卡片
化学式: C9H20O (144.151407)
中文名称: (R)-(-)-2-壬醇, (S)-(+)-2-壬醇, 2-壬基醇, 2-壬醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCCCCCC(C)O
InChI: InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3
描述信息
2-Nonanol, also known as 2-hydroxynonane or 2-nonyl alcohol, belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. 2-Nonanol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Thus, 2-nonanol is considered to be a fatty alcohol lipid molecule.
Isolated from various essential oils, orange (Citrus sinensis), ginger (Zingiber officinale), coconut (Coces nucifera)and is also present in guava fruit, raw asparagus, various cheeses and wines. 2-Nonanol is found in many foods, some of which are tea, cloves, milk and milk products, and citrus.
同义名列表
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:78304
- PubChem: 12367
- HMDB: HMDB0033916
- ChEMBL: CHEMBL454517
- Wikipedia: 2-Nonanol
- foodb: FDB012114
- chemspider: 11861
- CAS: 70419-06-6
- CAS: 70419-07-7
- CAS: 628-99-9
- PMhub: MS000167600
- RefMet: 2-Nonanol
- LOTUS: LTS0264829
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)
67 个相关的物种来源信息
- 4454 - Araceae: LTS0264829
- 4457 - Arum: LTS0264829
- 4458 - Arum maculatum: 10.1016/0305-1978(95)00026-Q
- 4458 - Arum maculatum: LTS0264829
- 186817 - Bacillaceae: LTS0264829
- 91061 - Bacilli: LTS0264829
- 1386 - Bacillus: LTS0264829
- 1392 - Bacillus anthracis: 10.1038/S41598-020-66136-0
- 1392 - Bacillus anthracis: LTS0264829
- 2 - Bacteria: LTS0264829
- 4441 - Camellia: LTS0264829
- 4442 - Camellia sinensis: 10.1021/JF00034A031
- 4442 - Camellia sinensis: LTS0264829
- 3481 - Cannabaceae: LTS0264829
- 99568 - Curcuma: LTS0264829
- 188487 - Etlingera: LTS0264829
- 188493 - Etlingera elatior: 10.1080/10412905.1993.9698191
- 188493 - Etlingera elatior: LTS0264829
- 3932 - Eucalyptus: LTS0264829
- 2759 - Eukaryota: LTS0264829
- 262 - Francisella: LTS0264829
- 263 - Francisella tularensis: 10.1038/S41598-020-66136-0
- 263 - Francisella tularensis: LTS0264829
- 34064 - Francisellaceae: LTS0264829
- 1236 - Gammaproteobacteria: LTS0264829
- 4027 - Geraniaceae: LTS0264829
- 9606 - Homo sapiens: -
- 3484 - Humulus: LTS0264829
- 3486 - Humulus lupulus: 10.1021/JF9911850
- 3486 - Humulus lupulus: LTS0264829
- 4447 - Liliopsida: LTS0264829
- 3398 - Magnoliopsida: LTS0264829
- 3931 - Myrtaceae: LTS0264829
- 59329 - Ophrys: LTS0264829
- 145953 - Ophrys sphegodes: 10.1016/S0031-9422(00)81276-5
- 145953 - Ophrys sphegodes: LTS0264829
- 882724 - Ophrys × arachnitiformis: 10.1016/S0031-9422(00)81276-5
- 145954 - Ophrys × splendida: 10.1016/S0031-9422(00)81276-5
- 4747 - Orchidaceae: LTS0264829
- 4030 - Pelargonium: LTS0264829
- 158596 - Pelargonium endlicherianum: 10.1055/S-2006-960872
- 158596 - Pelargonium endlicherianum: LTS0264829
- 4479 - Poaceae: LTS0264829
- 37564 - Ruta: LTS0264829
- 452789 - Ruta angustifolia: 10.1080/10412905.1991.9697956
- 452789 - Ruta angustifolia: LTS0264829
- 37565 - Ruta graveolens: 10.1055/S-0028-1097798
- 37565 - Ruta graveolens: 10.1080/10412905.1989.9697787
- 37565 - Ruta graveolens: LTS0264829
- 23513 - Rutaceae: LTS0264829
- 35493 - Streptophyta: LTS0264829
- 27065 - Theaceae: LTS0264829
- 58023 - Tracheophyta: LTS0264829
- 33090 - Viridiplantae: LTS0264829
- 4575 - Zea: LTS0264829
- 4577 - Zea mays:
- 4577 - Zea mays: 10.1021/JF60218A022
- 4577 - Zea mays: 10.1021/JF60230A020
- 4577 - Zea mays: LTS0264829
- 4650 - Zingiber: LTS0264829
- 136225 - Zingiber mioga: 10.1271/BBB1961.55.1655
- 136225 - Zingiber mioga: LTS0264829
- 94328 - Zingiber officinale:
- 94328 - Zingiber officinale: 10.1016/S0031-9422(00)84581-1
- 94328 - Zingiber officinale: 10.1021/JF00097A027
- 94328 - Zingiber officinale: LTS0264829
- 4642 - Zingiberaceae: LTS0264829
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
- Cong Song, Yang Zhang, Qian Zhao, Mengyao Chen, Yu Zhang, Congcong Gao, Zhenhua Jia, Shuishan Song, Junfeng Guan, Zhonglin Shang. Volatile organic compounds produced by Bacillus aryabhattai AYG1023 against Penicillium expansum causing blue mold on the Huangguan pear.
Microbiological research.
2023 Oct; 278(?):127531. doi:
10.1016/j.micres.2023.127531
. [PMID: 37871540] - Tomoko Toyama, Michiru Tahara, Kisaburo Nagamune, Kenji Arimitsu, Yoshio Hamashima, Nirianne M Q Palacpac, Hiroshi Kawaide, Toshihiro Horii, Kazuyuki Tanabe. Gibberellin biosynthetic inhibitors make human malaria parasite Plasmodium falciparum cells swell and rupture to death.
PloS one.
2012; 7(3):e32246. doi:
10.1371/journal.pone.0032246
. [PMID: 22412858] - Nikoletta G Ntalli, Francesca Manconi, Marco Leonti, Andrea Maxia, Pierluigi Caboni. Aliphatic ketones from Ruta chalepensis (Rutaceae) induce paralysis on root knot nematodes.
Journal of agricultural and food chemistry.
2011 Jul; 59(13):7098-103. doi:
10.1021/jf2013474
. [PMID: 21631118] - Ilya B Slizovskiy, Jason C White, Jason W Kelsey. Technical note: evaluation of extraction methodologies for the determination of an organochlorine pesticide residue in vegetation.
International journal of phytoremediation.
2010 Oct; 12(8):820-32. doi:
10.1080/15226510903390445
. [PMID: 21166351] - Anders I Seldén, Cecilia Lundholm, Niklas Johansson, Håkan Wingfors. Polychlorinated biphenyls (PCB), thyroid hormones and cytokines in construction workers removing old elastic sealants.
International archives of occupational and environmental health.
2008 Oct; 82(1):99-106. doi:
10.1007/s00420-008-0313-5
. [PMID: 18350309] - Steina Aradottir, Bo L Olsson. Methodological modifications on quantification of phosphatidylethanol in blood from humans abusing alcohol, using high-performance liquid chromatography and evaporative light scattering detection.
BMC biochemistry.
2005 Sep; 6(?):18. doi:
10.1186/1471-2091-6-18
. [PMID: 16188025] - Giorgis Isaac, Monica Waldebäck, Ulla Eriksson, Göran Odham, Karin E Markides. Total lipid extraction of homogenized and intact lean fish muscles using pressurized fluid extraction and batch extraction techniques.
Journal of agricultural and food chemistry.
2005 Jul; 53(14):5506-12. doi:
10.1021/jf0501286
. [PMID: 15998106] - E F L R A Patricio, L Cruz-López, E D Morgan. Electroantennography in the study of two stingless bee species (Hymenoptera: Meliponini).
Brazilian journal of biology = Revista brasleira de biologia.
2004 Nov; 64(4):827-31. doi:
10.1590/s1519-69842004000500012
. [PMID: 15744423]