N-Acetylhistamine (BioDeep_00000001295)

 

Secondary id: BioDeep_00000406237

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


N-(2-(1H-Imidazol-4-yl)ethyl)acetamide (acd/name 4.0)

化学式: C7H11N3O (153.09020759999999)
中文名称: N-乙酰组胺, N-ω-乙酰基组胺
谱图信息: 最多检出来源 Homo sapiens(feces) 0.08%

分子结构信息

SMILES: CC(=O)NCCC1=CN=CN1
InChI: InChI=1S/C7H11N3O/c1-6(11)9-3-2-7-4-8-5-10-7/h4-5H,2-3H2,1H3,(H,8,10)(H,9,11)

描述信息

N-Acetylhistamine is a 4-(beta-Acetylaminoethyl)imidazole that is an intermediate in Histidine metabolism. It is generated from Histamine via the enzyme Transferases (EC 2.3.1.-). Histamine is an amine derived by enzymatic decarboxylation of histidine. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
Isolated from leaves of Spinacia oleracea (spinach). N-Acetylhistamine is found in green vegetables and spinach.
KEIO_ID A093
N-Acetylhistamine is a histamine metabolite. N-acetylhistamine can be used as a potential biomarker of histidine metabolism for anaphylactoid reactions.
N-Acetylhistamine is a histamine metabolite. N-acetylhistamine can be used as a potential biomarker of histidine metabolism for anaphylactoid reactions.

同义名列表

33 个代谢物同义名

N-(2-(1H-Imidazol-4-yl)ethyl)acetamide (acd/name 4.0); Acetamide, N-(2-(1H-imidazol-4-yl)ethyl)- (9ci); Acetamide, {n-[2-(1H-imidazol-4-yl)ethyl]-}; Acetamide, N-(2-imidazol-4-ylethyl)- (8ci); N-[2-(1H-Imidazol-4-yl)ethyl]-acetamide; N-[2-(1H-imidazol-5-yl)ethyl]acetamide; N-(2-(1H-Imidazol-4-yl)ethyl)acetamide; N-[2-(3H-Imidazol-4-yl)ethyl]acetamide; N-[2-(1H-IMIDAZOL-4-yl)ethyl]acetamide; N-(2-(Imidazol-4-yl)ethyl)acetamide; N-(2-Imidazol-4-ylethyl)-acetamide; 4-(beta-Acetylaminoethyl)imidazole; 4-(2-Acetylaminoethyl)imidazole; 4-(b-Acetylaminoethyl)imidazole; 4-(Β-acetylaminoethyl)imidazole; 4-(2-Acetamidoethyl)imidazole; Imidazole C-4(5) deriv. 1; N-.Omega.-acetylhistamine; N-Omega-acetyl-histamine; Omega-N-acetylhistamine; N-Omega-acetylhistamine; alpha-N-Acetylhistamine; Nalpha-acetylhistamine; Nomega-acetylhistamine; N-ω-Acetylhistamine; a-N-Acetylhistamine; Α-N-acetylhistamine; Nw-Acetylhistamine; N-acetylhistamine; N-Acetylhistamine; Acetylhistamine; AHN; N-Acetylhistamine



数据库引用编号

28 个数据库交叉引用编号

分类词条

相关代谢途径

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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)

4 个相关的物种来源信息

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

  • Daniele Sanna, Linda Bíró, Péter Buglyó, Giovanni Micera, Eugenio Garribba. Transport of the anti-diabetic VO2+ complexes formed by pyrone derivatives in the blood serum. Journal of inorganic biochemistry. 2012 Oct; 115(?):87-99. doi: 10.1016/j.jinorgbio.2012.04.020. [PMID: 22926028]
  • Moses O Akiibinu, Omobola A Ogundahunsi, Ebenezer O Ogunyemi. Inter-relationship of plasma markers of oxidative stress and thyroid hormones in schizophrenics. BMC research notes. 2012 Mar; 5(?):169. doi: 10.1186/1756-0500-5-169. [PMID: 22463715]
  • H M ADAM, D C HARDWICK, K E SPENCER. A method of estimating histamine in plasma. British journal of pharmacology and chemotherapy. 1957 Dec; 12(4):397-405. doi: 10.1111/j.1476-5381.1957.tb00155.x. [PMID: 13489164]