53733-97-4 Usage
General Description
Z-BETA-ALA-OSU is a synthetic chemical compound designed for potential use in medical and pharmaceutical applications. It is a derivative of beta-alanine, an amino acid that plays a role in the synthesis of carnosine, a dipeptide with antioxidant and protective properties. Z-BETA-ALA-OSU has been studied for its potential as a prodrug, a compound that can be converted into a pharmacologically active form within the body. Research has also indicated that Z-BETA-ALA-OSU may have anti-inflammatory and neuroprotective properties, making it of interest for potential therapeutic applications in the treatment of conditions such as neurodegenerative diseases and chronic inflammatory disorders. Further study of this compound is needed to fully understand its potential uses and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 53733-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,3 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53733-97:
(7*5)+(6*3)+(5*7)+(4*3)+(3*3)+(2*9)+(1*7)=134
134 % 10 = 4
So 53733-97-4 is a valid CAS Registry Number.
53733-97-4Relevant articles and documents
Synthesis of amino acid derivatives of hydrazones and oximes of spirodihydropyranochromen-2-ones
Veselovska,Garazd,Ogorodniychuk,Garazd,Khilya
experimental part, p. 153 - 162 (2009/04/03)
Sulfur-and nitrogen-containing derivatives of spirodihydropyranochromen-2- ones at the exocyclic oxygen atom have been synthesized. Modification of the oximes and hydrazones of the spiro-substituted pyranocoumarins with N-substituted amino acids were carried out using activated ester and symmetrical anhydride methods.
Compositions for the delivery of negatively charged molecules
-
, (2008/06/13)
This invention features permeability enhancer molecules, and methods, to increase membrane permeability of negatively charged polymers thereby facilitating cellular uptake of such polymers.
Bridged isocytosine-adenosine compounds: Synthesis and antibacterial evaluation
Lever Jr.,Vestal
, p. 901 - 903 (2007/10/02)
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