咪唑-4-乙醛
| 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 
|
| PubChem | 150841 |
| ChemSpider | 132948 |
| SMILES |
|
| InChI |
|
| 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-乙醛或咪唑-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
- ^ 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.
- ^ 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.