13934-03-7 Usage
Uses
Used in Pharmaceutical Industry:
PYRIDOXYLIDENE-L-GLUTAMIC ACID DIPOTASSIUM SALT is used as a therapeutic agent for its antioxidant and neuroprotective properties, aiming to treat neurological diseases and conditions. Its ability to protect neurons and reduce oxidative stress makes it a valuable component in the development of medications for such health issues.
Used in Medicinal Applications:
In the medicinal field, PYRIDOXYLIDENE-L-GLUTAMIC ACID DIPOTASSIUM SALT is utilized for its potential to alleviate symptoms and improve the prognosis of patients with neurological disorders. Its antioxidant capabilities contribute to the mitigation of oxidative stress, a common factor in many neurological conditions, thereby offering a promising avenue for treatment and management.
Used in Research and Development:
PYRIDOXYLIDENE-L-GLUTAMIC ACID DIPOTASSIUM SALT is employed as a subject of research for further exploration of its potential benefits and mechanisms of action. Scientists and researchers investigate its interactions with biological systems and its potential synergistic effects with other compounds, aiming to enhance its therapeutic efficacy and broaden its applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 13934-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,3 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13934-03:
(7*1)+(6*3)+(5*9)+(4*3)+(3*4)+(2*0)+(1*3)=97
97 % 10 = 7
So 13934-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2O6.2K/c1-7-12(19)9(8(6-16)4-14-7)5-15-10(13(20)21)2-3-11(17)18;;/h4-5,10,16,19H,2-3,6H2,1H3,(H,17,18)(H,20,21);;/q;2*+1/p-2/b15-5+;;/t10-;;/m0../s1
13934-03-7Relevant academic research and scientific papers
Conformations of Pyridoxal Schiff Bases of Amino Acids. A Circular Dichroism Study
Casella, Luigi,Gullotti, Michele
, p. 803 - 809 (2007/10/02)
The conformations of a series of peridoxal-L-amino acid Schiff bases in methanol solution were deduced from their circular dichroism spectra.The N-salicylidene analogues of the pyridoxal Schiff bases were used as appropriate reference compounds.The predominant conformation of the Cα-N bond was found to be approximately the same for all the Schiff bases and involves a pseudoequatorial disposition of the Cα-H bond with respect to the plane of the extended ? system.The sign of the Cotton effects near 420 and 340 nm varies with the nature (polar, nonpolar, aromatic) of the amino acid side chain, according to the chirality of the dominant interaction of the amino acid residue with the pyridoxylideneamino chromophore.The circular dichroism spectra of zinc(II) complexes of N-pyridoxylidene-L-amino acids were also discussed in relation to the metal-free systems.
