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About This Item
Empirical Formula (Hill Notation):
C10H12N2O3
CAS Number:
Molecular Weight:
208.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
206-445-9
MDL number:
Beilstein/REAXYS Number:
2697333
Product Name
DL-Kynurenine, ≥95.0% (NT)
Quality Level
assay
≥95.0% (NT)
form
powder
mp
~235 °C (dec.)
application(s)
peptide synthesis
SMILES string
NC(CC(=O)c1ccccc1N)C(O)=O
InChI
1S/C10H12N2O3/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15/h1-4,8H,5,11-12H2,(H,14,15)
InChI key
YGPSJZOEDVAXAB-UHFFFAOYSA-N
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ye Lu et al.
Journal of clinical biochemistry and nutrition, 58(3), 210-215 (2016-06-04)
Postoperative fatigue syndrome is a general complication after surgery. However, there is no ''gold standard'' for fatigue assessment due to the lack of objective biomarkers. In this study, a rodent model of postoperative fatigue syndrome based on partial hepatectomy was
Adam K Walker et al.
Molecular psychiatry, 24(10), 1523-1532 (2018-07-11)
Inflammation activates indoleamine 2,3-dioxygenase (IDO) which metabolizes tryptophan into kynurenine. Circulating kynurenine is transported into the brain by the large amino transporter LAT1 at the level of the blood-brain barrier. We hypothesized that administration of leucine that has a high
László Vécsei et al.
Nature reviews. Drug discovery, 12(1), 64-82 (2012-12-15)
Various pathologies of the central nervous system (CNS) are accompanied by alterations in tryptophan metabolism. The main metabolic route of tryptophan degradation is the kynurenine pathway; its metabolites are responsible for a broad spectrum of effects, including the endogenous regulation
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 61250-1G | 04061826095416 |
| 61250-250MG | 04061832595276 |