77951
Imidazolepropionic acid
≥98.0% (GC)
동의어(들):
1H-Imidazole-4-propanoic acid, 1H-Imidazole-5-propanoic acid, 3-(1H-Imidazol-4-yl)propionic acid, 3-(Imidazol-4(5)-yl)propionic acid, Deamino-histidine, Dihydrourocanic acid, NSC 66737
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C6H8N2O2
CAS Number:
Molecular Weight:
140.14
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.25
추천 제품
Quality Level
분석
≥98.0% (GC)
양식
powder
저장 온도
2-8°C
SMILES string
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
생화학적/생리학적 작용
Imidazolepropionic acid is a product of histidine metabolism, which may involve oxidation or transamination
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
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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
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.
W D Block et al.
The Journal of nutrition, 91(2), 189-194 (1967-02-01)
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)
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)
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