77951
咪唑丙酸
≥98.0% (GC)
别名:
1H-咪唑-4-丙酸, 1H-咪唑-5-丙酸, 3-(1H-咪唑-4-基）丙酸, 3-（咪唑-4（5）-基）丙酸, NSC 66737, 二氢尿酸, 脱氨基组氨酸
质量水平
方案
≥98.0% (GC)
表单
powder
储存温度
2-8°C
SMILES字符串
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 key
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
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
I Antener et al.
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
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.
Roberts, J. D. , et al.
Journal of the American Chemical Society, 104, 3945-3949 (1982)
A covalent nicotinamide adenine dinucleotide intermediate in the urocanase reaction.
L H Matherly et al.
Biochemistry, 21(11), 2789-2794 (1982-05-25)
Alexander V Bogachev et al.
Molecular microbiology, 86(6), 1452-1463 (2012-10-20)
Interpretation of the constantly expanding body of genomic information requires that the function of each gene be established. Here we report the genomic analysis and structural modelling of a previously uncharacterized redox-metabolism protein UrdA (SO_4620) of Shewanella oneidensis MR-1, which
Imidazolepropionic acid as a urinary metabolite of L-histidine.
N P SEN et al.
Biochemical and biophysical research communications, 9, 257-261 (1962-10-17)
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