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L-Kynurenine sulfate salt , CAS No.16055-80-4
Basic Description Synonyms (S)-2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid,sulfuric acid | AKOS015911368 | (2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid;sulfuric acid | HY-104026B | L-KYNURENINESULFATE | MLS002207218 | 6-hydroxy-5-(2-phenyldiazenyl)-2-Naphthalenesulfonic acid Specifications & Purity ≥98% Biochemical and Physiological Mechanisms L-canurine is a key intermediate in the decomposition of L-tryptophan and formation of nicotinamide adenine dinucleotide (NAD +) through the canurine pathway. L-canurine is involved in a variety of neurological processes and diseases. L-canuridine is the Storage Temp Store at -20°C Shipped In Ice chest + Ice pads
Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Names and Identifiers IUPAC Name (2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid;sulfuric acid INCHI 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 Canonical SMILES C1=CC=C(C(=C1)C(=O)CC(C(=O)O)N)N.OS(=O)(=O)O Isomeric SMILES C1=CC=C(C(=C1)C(=O)C[C@@H](C(=O)O)N)N.OS(=O)(=O)O PubChem CID 161165 Molecular Weight 306.29
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C2309770