추천 제품
분석
≥98.0% (GC)
형태
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
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
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.
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)
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.
Biochemical and biophysical research communications, 9, 257-261 (1962-10-17)
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