62700-65-6 Usage
Chemical composition
2-(methylsulfanyl)-7H-purin-6-amine hydrochloride is a chemical compound that contains a purine base with a methylthio group attached to the 2-position.
Derivative of adenine
It is a derivative of adenine, a nucleobase that is a component of DNA and RNA.
Salt form
The hydrochloride salt form of 2-(methylsulfanyl)-7H-purin-6-amine hydrochloride is commonly used in biochemical and pharmaceutical research.
Biological activity
It is a selective adenosine A2A receptor agonist.
Potential therapeutic applications
It has been studied for its potential use in treating various disorders such as Parkinson's disease, inflammation, and certain types of cancer.
Neuroprotective properties
Research has also shown its potential as a protective agent against neurodegenerative diseases.
Role in therapeutic strategies
2-(methylsulfanyl)-7H-purin-6-amine hydrochloride holds a significant role in the development of novel therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 62700-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,0 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62700-65:
(7*6)+(6*2)+(5*7)+(4*0)+(3*0)+(2*6)+(1*5)=106
106 % 10 = 6
So 62700-65-6 is a valid CAS Registry Number.
62700-65-6Relevant academic research and scientific papers
EFFECT OF SUBSTITUENT AT C2 ON THE DIRECTION OF ELECTROPHILIC ATTACK IN ADENINES. METHYLATION AND PROTONATION OF 2-METHYLTHIO-6-AMINOPURINE DERIVATIVES
Muravich-Aleksandr, Kh. L.,Pernikoza, V. G.,Ragozina, T. N.
, p. 767 - 775 (2007/10/02)
The directions of methylation and protonation in 2-methylthio-6-aminopurine and its 3-, 7-, and 9-methyl derivatives only coincide in the case of the 3- and 7- methyl derivatives, whereas methylation of the 9-methyl isomer takes place mainly at N7 and protonation at N1.A proposal is made about the role of steric hindrances created by the ortho substituent to attack by the methyl at N1.The compounds form dications in trifluoroacetic acid.
