94535-32-7 Usage
Uses
Used in Pharmaceutical Industry:
(+-)-6-Amino-alpha-hydroxy-9H-purine-9-propanoic acid is used as a pharmaceutical candidate for its potential biological activity due to its purine structure, which is a common component of nucleic acids and various other important biomolecules. The presence of an amino and hydroxy group also suggests potential for involvement in biochemical reactions or interactions with biological systems, making it a promising compound for further research and development in the pharmaceutical field.
Used in Biochemical Research:
(+-)-6-Amino-alpha-hydroxy-9H-purine-9-propanoic acid is used as a research compound for studying its potential biological activity and interactions with biological systems. Its unique molecular structure, including the purine backbone, amino, and hydroxy groups, as well as the propanoic acid moiety, makes it an interesting subject for investigation in biochemical research to understand its properties and potential applications.
Further research and analysis would be necessary to fully understand the properties and potential uses of this chemical compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 94535-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94535-32:
(7*9)+(6*4)+(5*5)+(4*3)+(3*5)+(2*3)+(1*2)=147
147 % 10 = 7
So 94535-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N5O3/c9-6-5-7(11-2-10-6)13(3-12-5)1-4(14)8(15)16/h2-4,14H,1H2,(H,15,16)(H2,9,10,11)
94535-32-7Relevant academic research and scientific papers
Alkyl esters of 3-adenin-9-yl-2-hydroxypropanoic acid: A new class of broad-spectrum antiviral agents
De Clercq,Holy
, p. 282 - 287 (2007/10/02)
A new class of acyclic adenosine analogues is described which exhibit broad-spectrum antiviral activity and are apparently targeted at S-adenosyl-L-homocysteine hydrolase. The compounds are all alkyl (i.e., methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methylpropyl, tert-butyl, 1-pentyl, 3-methylbutyl, 1-octyl, 2-hydroxyethyl, 2-methoxyethyl, furylmethyl, cyclohexyl) esters of (RS)-3-adenin-9-yl-2-hydroxypropanoic acid. They are inhibitory to a broad variety of viruses, including vesicular stomatitis, vaccinia, reo, parainfluenza, and measles, and with one exception (the furylmethyl ester), nontoxic to the host cell at antivirally active concentrations. It is postulated that the alkyl esters are as such taken up by the cells and hydrolyzed within the cells to release the parent compound, 3-adenin-9-yl-2-hydroxypropanoic acid.
