L-KYNURENINE

L-KYNURENINE Basic information
Product Name:L-KYNURENINE
Synonyms:L-2-AMINO-3-(2-AMINOBENZOYL)PROPIONIC ACID;L-2-AMINO-4-[2-AMINOPHENYL]-4-OXOBUTANOIC ACID;L-KYNURENINE;L-kynurenine free base;β-Anthraniloyl-L-alanine;β-Anthraniloyl-L-alanine, L-2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid;L-Kynurenine Hydrate;(S)-2-Amino-4-oxo-4-(2-aminophenyl)butanoic acid
CAS:2922-83-0
MF:C10H12N2O3
MW:208.21
EINECS:
Product Categories:Amino Acids;Amino Acids;Biochemistry;non-Proteinorganic Amino Acids
Mol File:2922-83-0.mol
L-KYNURENINE Structure
L-KYNURENINE Chemical Properties
Melting point 219 °C
Boiling point 466.6±45.0 °C(Predicted)
density 1.343±0.06 g/cm3(Predicted)
refractive index -33 ° (C=0.4, H2O)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility Soluble in DMSO (up to 2 mg/ml) or in Water (up to 2 mg/ml).
form crystalline
pka2.21±0.23(Predicted)
color light yellow
Merck 14,5328
Stability:Stable for 2 years as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 3 months.
InChIKeyYGPSJZOEDVAXAB-QMMMGPOBSA-N
CAS DataBase Reference2922-83-0(CAS DataBase Reference)
Safety Information
WGK Germany 3
RTECS CY9049700
HS Code 2922500090
MSDS Information
ProviderLanguage
SigmaAldrich English
L-KYNURENINE Usage And Synthesis
DescriptionKynurenine (2922-83-0) is a tryptophan catabolite.1?Endogenous tumor-promoting ligand of the human aryl hydrocarbon receptor (AhR). Constitutively generated by human tumor cells via the action of the tryptophan degrading enzyme, tryptophan-2,3-dioxygenase (TDO). Kynurenine suppresses antitumor immune responses and promotes tumor cell survival and motility.2
UsesL-Kynurenine has been used as a standard for indoleamine-2,3-dioxygenase (IDO) assay. It has also been used as a standard to extract and quantify kynurenine from cultured cells and media.
DefinitionChEBI: A kynurenine that has L configuration.
Biochem/physiol ActionsKey intermediate in the breakdown pathway of tryptophan.
storageStore at RT
ReferencesReferences/Citations 1) Ibana?et al. (2011),?Inhibition of indoleamine 2,3-dioxygenase activity by levo-1-methyl tryptophan blocks gamma interferon-induced Chlaydia trachomatis persistence in human epithelial cells; Infect. Immun.,?79?4425 2) Opitz?et al. (2011),?An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor; Nature,?478?197
HYDROXY-DL-KYNURENINE, 3-(RG) Kynurenine yellow L-Kynurenine diacetate L-KYNURENINE SULFATE,L-KYNURENINE SULFATE SALT KYNURENINE SULFATE L-,L-KYNURENINE SULFATE MONOHYDRATE,L-KYNURENINE SULFATE KYNURENINE SULFATE L-(RG) dl-kynurenine sulfate,DL-KYNURENINE SULFATE (SALT) MONOHYDRATE,DL-KYNURENINE SULFATE SALT L-KYNURENINE SULFATE (SALT) MONOHYDRATE kynurenine 3-monooxygenase Fmoc-L-Kynurenine kynurenine 62-lysozyme 3-HYDROXY-DL-KYNURENINE,HYDROXY-DL-KYNURENINE, 3- D-kynurenine free base,D-KYNURENINE kynurenine-oxoglutarate transaminase DL-KYNURENINE SULFATE MONOHYDRATE,DL-KYNURENINE SULPHATE MONOHYDRATE kynurenine receptor dl-Kynurenine-13C3 FMOC-KYNURENINE

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