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咪唑-4-乙醛

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咪唑-4-乙醛
別名 1H-Imidazole-5-acetaldehyde, 1H-Imidazole-5-acetaldehyde, Imidazole-4-acetaldehyde, 1H-Imidazole-4-acetaldehyde, Imidazole-5-acetaldehyde, 4-Imidazolylacetaldehyde, 2-(1H-Imidazol-4-yl)acetaldehyde, 2-(1H-Imidazol-5-yl)acetaldehyde
識別
CAS號 645-14-7  checkY
PubChem 150841
ChemSpider 132948
SMILES
 
  • C1=C(NC=N1)CC=O
InChI
 
  • 1S/C5H6N2O/c8-2-1-5-3-6-4-7-5/h2-4H,1H2,(H,6,7)
InChIKey MQSRGWNVEZRLDK-UHFFFAOYSA-N
ChEBI 27398
KEGG C05130
性質
化學式 C5H6N2O
摩爾質量 110.11 g·mol⁻¹
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

咪唑-4-乙醛咪唑-5-乙醛是一種有機氮化合物,化學式為C5H6N2O,它是組胺的代謝產物。它可以被NAD依賴性乙醛脫氫酶進一步氧化,生成咪唑-4-乙酸[1][2]

參考文獻

[編輯]
  1. ^ Bähre H, Kaever V. Analytical Methods for the Quantification of Histamine and Histamine Metabolites. Handb Exp Pharmacol. Handbook of Experimental Pharmacology. 2017, 241: 3–19. ISBN 978-3-319-58192-7. PMID 28321587. doi:10.1007/164_2017_22. 
  2. ^ Ambroziak W, Maśliński C. Participation of aldehyde dehydrogenase in the oxidative deamination pathway of histamine and putrescine. Agents Actions. April 1988, 23 (3–4): 311–3. PMID 3394581. S2CID 8283492. doi:10.1007/BF02142573.