2-Pentanol (BioDeep_00000019453)
human metabolite Volatile Flavor Compounds natural product
代谢物信息卡片
化学式: C5H12O (88.0888102)
中文名称: 2-戊醇, 仲戊醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCC(C)O
InChI: InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3
描述信息
2-Pentanol, also known as 1-methylbutanol or 2-hydroxypentane, belongs to the class of organic compounds known as secondary alcohols. A secondary alcohol that is pentane substituted at position 2 by a hydroxy group. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R) (R,R=alkyl, aryl). 2-Pentanol has been detected, but not quantified, in a few different foods, such as alcoholic beverages, fruits, and milk and milk products.
Present in many foodstuffs, e.g. fruits, alcoholic beverages and cheeses. xi-2-Pentanol is found in alcoholic beverages, milk and milk products, and fruits.
同义名列表
32 个代谢物同义名
Isoamyl alcohol (primary/secondary; Isoamyl alcohol, secondary; Methyl propyl carbinol; Methylpropylcarbinol; alpha-Methylbutanol; Potassium t-amylate; Sec-N-amyl alcohol; (S)-(+)-2-Pentanol; 1-Methyl-1-butanol; 2-METHYL-2-BUTANOL; Sec-pentyl alcohol; (R)-(-)-2-Pentanol; tert-Amyl Alcohol; Sec-amyl alcohol; 2-Pentyl alcohol; 2-Hydroxypentane; (+/-)-2-pentanol; Methylbutan-1-ol; a-Methylbutanol; N-C3H7CH(OH)CH3; Α-methylbutanol; 1-Methylbutanol; t-Amyl alcohol; Methyl-butanol; Methyl butanol; xi-2-Pentanol; Sec-pentanol; Pentan-2-ol; 2-PENTANOL; Pentanol-2; FEMA 3316; 2-Pentanol
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:77518
- PubChem: 22386
- HMDB: HMDB0031599
- ChEMBL: CHEMBL45065
- Wikipedia: 2-Pentanol
- foodb: FDB011151
- chemspider: 21011
- CAS: 51000-78-3
- CAS: 50858-14-5
- CAS: 26635-63-2
- CAS: 6032-29-7
- PMhub: MS000016561
- LOTUS: LTS0217254
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)
49 个相关的物种来源信息
- 4210 - Asteraceae: LTS0217254
- 4441 - Camellia: LTS0217254
- 4442 - Camellia sinensis: 10.1248/CPB.55.598
- 4442 - Camellia sinensis: LTS0217254
- 13426 - Cichorium: LTS0217254
- 114280 - Cichorium endivia: 10.1021/JF00068A014
- 114280 - Cichorium endivia: LTS0217254
- 4345 - Ericaceae: LTS0217254
- 2759 - Eukaryota: LTS0217254
- 3803 - Fabaceae: LTS0217254
- 9606 - Homo sapiens: -
- 4136 - Lamiaceae: LTS0217254
- 4447 - Liliopsida: LTS0217254
- 3398 - Magnoliopsida: LTS0217254
- 3629 - Malvaceae: LTS0217254
- 3877 - Medicago: LTS0217254
- 3879 - Medicago sativa: 10.1016/S0031-9422(97)00119-2
- 3879 - Medicago sativa: LTS0217254
- 4640 - Musa: LTS0217254
- 89151 - Musa × paradisiaca: 10.1021/JF00035A046
- 4637 - Musaceae: LTS0217254
- 4479 - Poaceae: LTS0217254
- 21880 - Salvia: LTS0217254
- 39367 - Salvia rosmarinus: 10.1111/J.1365-2621.1985.TB10476.X
- 39367 - Salvia rosmarinus: LTS0217254
- 35493 - Streptophyta: LTS0217254
- 27065 - Theaceae: LTS0217254
- 3640 - Theobroma: LTS0217254
- 3641 - Theobroma cacao: 10.1021/JF60160A011
- 3641 - Theobroma cacao: LTS0217254
- 58023 - Tracheophyta: LTS0217254
- 13749 - Vaccinium: LTS0217254
- 13750 - Vaccinium macrocarpon: 10.3891/ACTA.CHEM.SCAND.21-2076
- 13750 - Vaccinium macrocarpon: LTS0217254
- 180772 - Vaccinium vitis-idaea: 10.3891/ACTA.CHEM.SCAND.21-0945
- 180772 - Vaccinium vitis-idaea: 10.3891/ACTA.CHEM.SCAND.21-2076
- 180772 - Vaccinium vitis-idaea: LTS0217254
- 33090 - Viridiplantae: LTS0217254
- 3602 - Vitaceae: LTS0217254
- 3603 - Vitis: LTS0217254
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 29760 - Vitis vinifera: LTS0217254
- 4575 - Zea: LTS0217254
- 4577 - Zea mays: 10.1021/JF60220A012
- 4577 - Zea mays: LTS0217254
- 4650 - Zingiber: LTS0217254
- 94328 - Zingiber officinale: 10.1021/JF00097A027
- 94328 - Zingiber officinale: LTS0217254
- 4642 - Zingiberaceae: LTS0217254
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
- Diem-Kieu Nguyen, Tri-Phuong Nguyen, Yi-Rong Li, Masaru Ohme-Takagi, Zin-Huang Liu, Thach-Thao Ly, Van-Anh Nguyen, Ngoc-Nam Trinh, Hao-Jen Huang. Comparative study of two indoor microbial volatile pollutants, 2-Methyl-1-butanol and 3-Methyl-1-butanol, on growth and antioxidant system of rice (Oryza sativa) seedlings.
Ecotoxicology and environmental safety.
2024 Mar; 272(?):116055. doi:
10.1016/j.ecoenv.2024.116055
. [PMID: 38340597] - Sarathadevi Rajendran, Patrick Silcock, Phil Bremer. Volatile Organic Compounds (VOCs) Produced by Levilactobacillus brevis WLP672 Fermentation in Defined Media Supplemented with Different Amino Acids.
Molecules (Basel, Switzerland).
2024 Feb; 29(4):. doi:
10.3390/molecules29040753
. [PMID: 38398505] - Tu-Trinh Thi Truong, Chi-Chou Chiu, Pei-Yu Su, Jing-Yu Chen, Tri-Phuong Nguyen, Masaru Ohme-Takagi, Ruey-Hua Lee, Wan-Hsing Cheng, Hao-Jen Huang. Signaling pathways involved in microbial indoor air pollutant 3-methyl-1-butanol in the induction of stomatal closure in Arabidopsis.
Environmental science and pollution research international.
2024 Jan; 31(5):7556-7568. doi:
10.1007/s11356-023-31641-y
. [PMID: 38165546] - Mikael A Molander, Inis B Winde, Joseph Burman, Franklin N Nyabuga, Tobias U T Lindblom, Lawrence M Hanks, Jocelyn G Millar, Mattias C Larsson. Common Cerambycid Pheromone Components as Attractants for Longhorn Beetles (Cerambycidae) Breeding in Ephemeral Oak Substrates in Northern Europe.
Journal of chemical ecology.
2019 Jul; 45(7):537-548. doi:
10.1007/s10886-019-01082-4
. [PMID: 31254146] - Xiang Ma, Erpei Wang, Yuyun Lu, Yong Wang, Shiyi Ou, Rian Yan. Acylation of Antioxidant of Bamboo Leaves with Fatty Acids by Lipase and the Acylated Derivatives' Efficiency in the Inhibition of Acrylamide Formation in Fried Potato Crisps.
PloS one.
2015; 10(6):e0130680. doi:
10.1371/journal.pone.0130680
. [PMID: 26098744] - Jacek Sein Anand, Joanna Gieroń, Wojciech Lechowicz, Daria Schetz, Maria Kała, Wojciech Waldman. Acute intoxication due to tert-amyl alcohol--a case report.
Forensic science international.
2014 Sep; 242(?):e31-e33. doi:
10.1016/j.forsciint.2014.07.020
. [PMID: 25112153] - Sonia Moreno-Perez, Marco Filice, Jose M Guisan, Gloria Fernandez-Lorente. Synthesis of ascorbyl oleate by transesterification of olive oil with ascorbic acid in polar organic media catalyzed by immobilized lipases.
Chemistry and physics of lipids.
2013 Sep; 174(?):48-54. doi:
10.1016/j.chemphyslip.2013.06.003
. [PMID: 23891831] - Bédis Dridi, Marie-Laure Fardeau, Bernard Ollivier, Didier Raoult, Michel Drancourt. Methanomassiliicoccus luminyensis gen. nov., sp. nov., a methanogenic archaeon isolated from human faeces.
International journal of systematic and evolutionary microbiology.
2012 Aug; 62(Pt 8):1902-1907. doi:
10.1099/ijs.0.033712-0
. [PMID: 22859731] - Pious Thomas. Long-term survival of Bacillus spores in alcohol and identification of 90\% ethanol as relatively more spori/bactericidal.
Current microbiology.
2012 Feb; 64(2):130-9. doi:
10.1007/s00284-011-0040-0
. [PMID: 22057920] - Sinikka Vainiotalo, Vesa Riihimäki, Kaija Pekari, Eija Teräväinen, Antero Aitio. Toxicokinetics of methyl tert-butyl ether (MTBE) and tert-amyl methyl ether (TAME) in humans, and implications to their biological monitoring.
Journal of occupational and environmental hygiene.
2007 Oct; 4(10):739-50. doi:
10.1080/15459620701551540
. [PMID: 17668360] - Susan C J Sumner, Derek B Janszen, Bahman Asgharian, Timothy A Moore, Horace D Parkinson, Timothy R Fennell. Species and gender differences in the metabolism and distribution of tertiary amyl methyl ether in male and female rats and mice after inhalation exposure or gavage administration.
Journal of applied toxicology : JAT.
2003 Nov; 23(6):427-36. doi:
10.1002/jat.931
. [PMID: 14635267] - Saskia M van Ruth, Carmel King, Persephoni Giannouli. Influence of lipid fraction, emulsifier fraction, and mean particle diameter of oil-in-water emulsions on the release of 20 aroma compounds.
Journal of agricultural and food chemistry.
2002 Apr; 50(8):2365-71. doi:
10.1021/jf011072s
. [PMID: 11929298] - A Amberg, U Bernauer, D Scheutzow, W Dekant. Biotransformation of [(12)C]- and [(13)C]-tert-amyl methyl ether and tert-amyl alcohol.
Chemical research in toxicology.
1999 Oct; 12(10):958-64. doi:
10.1021/tx990078x
. [PMID: 10525272] - A S Collins, S C Sumner, S J Borghoff, M A Medinsky. A physiological model for tert-amyl methyl ether and tert-amyl alcohol: hypothesis testing of model structures.
Toxicological sciences : an official journal of the Society of Toxicology.
1999 May; 49(1):15-28. doi:
10.1093/toxsci/49.1.15
. [PMID: 10367338]