추천 제품
product name
L-Kynurenine sulfate salt, crystalline
분석
≥98% (HPLC)
형태
crystalline
기술
ligand binding assay: suitable
색상
light yellow
저장 온도
−20°C
SMILES string
OS(O)(=O)=O.N[C@@H](CC(=O)c1ccccc1N)C(O)=O
InChI
1S/C10H12N2O3.H2O4S/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15;1-5(2,3)4/h1-4,8H,5,11-12H2,(H,14,15);(H2,1,2,3,4)/t8-;/m0./s1
InChI key
KAXRWMOLNJZCEW-QRPNPIFTSA-N
관련 카테고리
애플리케이션
L-Kynurenine sulfate salt has been used as a substrate to study the enzyme activity of kynurenine aminotransferase. It has also been used in the synthesis of Kyn adducts of certain amino acids .
생화학적/생리학적 작용
L-Kynurenine (L-Kyn) is a precursor of kynurenic acid which is the only recognized endogenous excitatory amino acid receptor antagonist in the central nervous system. L-Kyn is known to be a pigment generating component in animals. In mammals, it modulates the transmission of glutamate neurotransmitter. It is also considered to be a sex-attracting pheromone in vertebrates.
L-Kynurenine is a key intermediate in the breakdown of L-tryptophan and the formation of nicotinamide adenine dinucleotide (NAD+) via the kynurenine pathway. L-kynurenine is involved in a variety of neurological processes and diseases. L-kynurenine is a substrate for kynureninase/kynurenine hydrolase; kynurenine 3-monooxygenase and kynurenine-oxoglutarate transaminase.
Key intermediate in the breakdown pathway of tryptophan.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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
Novel protein modification by kynurenine in human lenses.
The Journal of Biological Chemistry, 277(7), 4867-4873 (2002)
L-Kynurenine, an amino acid identified as a sex pheromone in the urine of ovulated female masu salmon.
Proceedings of the National Academy of Sciences of the USA, 103(42), 15370-15374 (2006)
Bioorganic & medicinal chemistry, 19(24), 7590-7596 (2011-11-15)
The overactivation of excitatory amino acid receptors plays a key role in the pathomechanism of several neurodegenerative disorders and in ischemic and post-ischemic events. Kynurenic acid (KYNA) is an endogenous product of the tryptophan metabolism and, as a broad-spectrum antagonist
Neuroprotective effects of L-kynurenine on hypoxia-ischemia and NMDA lesions in neonatal rats.
Journal of Cerebral Blood Flow and Metabolism, 12(3), 400-407 (1992)
Mitochondrial aspartate aminotransferase: a third kynurenate-producing enzyme in the mammalian brain.
Journal of Neurochemistry, 102(1), 103-111 (2007)
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