化驗
≥98.0% (GC)
形狀
powder
儲存溫度
2-8°C
SMILES 字串
OC(CCC1=CN=CN1)=O
InChI
1S/C6H8N2O2/c9-6(10)2-1-5-3-7-4-8-5/h3-4H,1-2H2,(H,7,8)(H,9,10)
InChI 密鑰
ZCKYOWGFRHAZIQ-UHFFFAOYSA-N
生化/生理作用
咪唑丙酸是组氨酸代谢的产物,可能涉及氧化或氨基转移
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 53(2), 199-209 (1983-01-01)
The present study, as a part of a broader investigation on protein-energy-malnutrition (PEM) in rural Zaire, was undertaken in order to clarify varying aspects of histidine metabolism in patients suffering from protein-energy malnutrition (PEM). Measurement of histidine and its derivatives
Histidine metabolism in the human adult: histidine blood tolerance, and the effect of continued free L-histidine ingestion on the concentration of imidazole compounds in blood and urine.
The Journal of nutrition, 91(2), 189-194 (1967-02-01)
Imidazolepropionic acid as a urinary metabolite of L-histidine.
Biochemical and biophysical research communications, 9, 257-261 (1962-10-17)
A nitrogen-15 nuclear magnetic resonance study of the acid-base and tautomeric equilibriums of 4-substituted imidazoles and its relevance to the catalytic mechanism of .alpha.-lytic protease.
Journal of the American Chemical Society, 104, 3945-3949 (1982)
A covalent nicotinamide adenine dinucleotide intermediate in the urocanase reaction.
Biochemistry, 21(11), 2789-2794 (1982-05-25)
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