N-Acetylputrescine (BioDeep_00000001393)
Secondary id: BioDeep_00000399964
natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019
代谢物信息卡片
化学式: C6H14N2O (130.1106)
中文名称: N-(4-氨基丁基)乙酰胺, N-(4-氨基丁基)-乙酰胺, N-乙酰腐胺, N-(4-氨基丁基)-乙酰胺 盐酸盐
谱图信息:
最多检出来源 Homo sapiens(blood) 9.59%
Last reviewed on 2024-09-13.
Cite this Page
N-Acetylputrescine. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/n-acetylputrescine (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000001393). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CC(=O)NCCCCN
InChI: InChI=1S/C6H14N2O/c1-6(9)8-5-3-2-4-7/h2-5,7H2,1H3,(H,8,9)
描述信息
N-Acetylputrescine is a polyamine commonly occurring excreted in normal human urine (PMID 7775374). N-Acetylputrescine is the most abundant of all polyamines both in normal individuals and in patients with leukemia (PMID 9464484). N-Acetylputrescine is the N-acetylated form of the naturally occurring polyamine called putrescine. The N-acetylation is mediated by the enzyme diamine N-acetyltransferase. Putrescine is related to cadaverine (another polyamine). Both are produced by the breakdown of amino acids in living and dead organisms and both are toxic in large doses. Putrescine and cadaverine are largely responsible for the foul odor of putrefying flesh, but also contribute to the odor of such processes as bad breath and bacterial vaginosis. Putrescine is also found in semen. Putrescine attacks s-adenosyl methionine and converts it to spermidine. Spermidine in turn attacks another s-adenosyl methionine and converts it to spermine. Putrescine is synthesized in small quantities by healthy living cells by the action of ornithine decarboxylase. N-Acetylputrescine can be found in Corynebacterium as well (PMID:25919117).
N-Acetylputrescine is a polyamine commonly occurring excreted in normal human urine (PMID 7775374). N-Acetylputrescine is the most abundant of all polyamines both in normal individuals and in patients with leukemia (PMID 9464484). N-Acetylputrescine is the N-acetylated form of the naturally occurring polyamine called putrescine. The N-acetylation is mediated by the enzyme diamine N-acetyltransferase. Putrescine is related to cadaverine (another polyamine). Both are produced by the breakdown of amino acids in living and dead organisms and both are toxic in large doses. Putrescine and cadaverine are largely responsible for the foul odor of putrefying flesh, but also contribute to the odor of such processes as bad breath and bacterial vaginosis. Putrescine is also found in semen. Putrescine attacks s-adenosyl methionine and converts it to spermidine. Spermidine in turn attacks another s-adenosyl methionine and converts it to spermine. Putrescine is synthesized in small quantities by healthy living cells by the action of ornithine decarboxylase. [HMDB]
Acquisition and generation of the data is financially supported in part by CREST/JST.
KEIO_ID A051
同义名列表
数据库引用编号
29 个数据库交叉引用编号
- ChEBI: CHEBI:17768
- KEGG: C02714
- PubChem: 122356
- HMDB: HMDB0002064
- Metlin: METLIN3252
- ChEMBL: CHEMBL81241
- MetaCyc: CPD-569
- foodb: FDB022827
- chemspider: 109095
- CAS: 18233-70-0
- CAS: 5699-41-2
- MoNA: KO002150
- MoNA: KO002149
- MoNA: PS049901
- MoNA: PR100276
- MoNA: KO002148
- MoNA: KO002151
- MoNA: PS049902
- MoNA: KO002152
- MoNA: PS049904
- MoNA: PS049903
- PMhub: MS000000436
- PubChem: 5677
- PDB-CCD: X5A
- 3DMET: B01596
- NIKKAJI: J367.698F
- RefMet: N-Acetylputrescine
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-290
- KNApSAcK: 17768
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
4 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- putrescine degradation III:
N-acetylputrescine + H2O + O2 ⟶ 4-acetamidobutanal + ammonia + hydrogen peroxide
- putrescine degradation III:
N-acetylputrescine + H2O + O2 ⟶ 4-acetamidobutanal + ammonia + hydrogen peroxide
Plant Reactome(0)
INOH(1)
- Arginine and Proline metabolism ( Arginine and Proline metabolism ):
ATP + Creatine ⟶ ADP + N-Phospho-creatine
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
9 个相关的物种来源信息
- 654 - Aeromonas veronii: 10.3389/FCIMB.2020.00044
- 3055 - Chlamydomonas reinhardtii: 10.1074/JBC.M110.122812
- 7227 - Drosophila melanogaster: 10.1038/S41467-019-11933-Z
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 9606 - Homo sapiens: -
- 9606 - Homo sapiens: 10.1007/S11306-016-1051-4
- 5691 - Trypanosoma brucei: 10.1371/JOURNAL.PNTD.0001618
- 29760 - Vitis vinifera: 10.1016/J.DIB.2020.106469
- 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
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Rheumatology (Oxford, England).
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10.1093/rheumatology/keaa125
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Journal of integrative plant biology.
2020 May; 62(5):601-613. doi:
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Scientific reports.
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Plant physiology.
2016 06; 171(2):1443-55. doi:
10.1104/pp.16.00446
. [PMID: 27208290] - Alberto Valdés, Virginia García-Cañas, Carolina Simó, Clara Ibáñez, Vicente Micol, Jose A Ferragut, Alejandro Cifuentes. Comprehensive foodomics study on the mechanisms operating at various molecular levels in cancer cells in response to individual rosemary polyphenols.
Analytical chemistry.
2014 Oct; 86(19):9807-15. doi:
10.1021/ac502401j
. [PMID: 25188358] - Daniela Münch, Terry Roemer, Sang Ho Lee, Marianne Engeser, Hans Georg Sahl, Tanja Schneider. Identification and in vitro analysis of the GatD/MurT enzyme-complex catalyzing lipid II amidation in Staphylococcus aureus.
PLoS pathogens.
2012 Jan; 8(1):e1002509. doi:
10.1371/journal.ppat.1002509
. [PMID: 22291598] - Ana Marta Silva, Anabela Cordeiro-da-Silva, Graham H Coombs. Metabolic variation during development in culture of Leishmania donovani promastigotes.
PLoS neglected tropical diseases.
2011 Dec; 5(12):e1451. doi:
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Cancer letters.
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BMC evolutionary biology.
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1982 Dec; 233(?):29-38. doi:
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