10082-93-6 Usage
Description
(9H-PURIN-6-YLAMINO)ACETIC ACID, a chemical compound with the molecular formula C9H9N5O2, is a derivative of purine and belongs to the class of compounds known as purine nucleobases and analogues. It is characterized by its unique chemical structure and properties, making it a valuable tool in drug discovery and development, as well as for understanding the biochemical processes associated with purine metabolism.
Uses
Used in Pharmaceutical Applications:
(9H-PURIN-6-YLAMINO)ACETIC ACID is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new drugs with potential therapeutic benefits.
Used in Anticancer Research:
In the field of oncology, (9H-PURIN-6-YLAMINO)ACETIC ACID is studied for its potential as an anticancer agent, targeting various types of cancer and modulating key signaling pathways involved in tumor growth and progression.
Used in Antiviral Research:
(9H-PURIN-6-YLAMINO)ACETIC ACID is also explored for its potential in antiviral treatments, offering a promising avenue for the development of new antiviral drugs to combat viral infections.
Used in Research and Development:
As a valuable tool in research, (9H-PURIN-6-YLAMINO)ACETIC ACID aids in understanding the biochemical processes associated with purine metabolism, which is crucial for the advancement of scientific knowledge and the development of novel therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 10082-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,8 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10082-93:
(7*1)+(6*0)+(5*0)+(4*8)+(3*2)+(2*9)+(1*3)=66
66 % 10 = 6
So 10082-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N5O2/c13-4(14)1-8-6-5-7(10-2-9-5)12-3-11-6/h2-3,5H,1H2,(H,13,14)(H,8,9,10,11,12)
10082-93-6Relevant articles and documents
Synthesis of N6-substituted adenines from 3-methylxanthine
Kochergin,Persanova,Aleksandrova
, p. 455 - 458 (2000)
A series of 6-arylalkyl(hetarylalkyl, cycloalkyl, carboxyalkyl)amino-7-benzyl-2-chloropurines have been synthesized from 3-methylxanthine via the reaction of the intermediate 7-benzyl-2,6-dichloropurine with amines and aminoacids. N6-benzyladenine, N6-(α-furfuryl)adenine (kinetin), and N-(purinyl)glycine have been obtained via the catalytic hydrogenation of 7-benzyl-6-benzyl(furfuryl, carboxymethyl)amino-2-chloropurines.
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Chheda,Hall
, p. 2082,2085 (1966)
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