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(R)-9-(1-methyl-2-hydroxyethyl)adenine, also known as 6-Methyl-1-ribofuranosyl-9H-purin-6-amine, is a chemical compound that belongs to the class of adenine nucleosides. It is a derivative of adenine and ribose, and the presence of a methyl group and a hydroxyethyl group in its structure gives it unique properties and potential biological activities. (R)-9-(1-methyl-2-hydroxyethyl)adeninde has been studied for its potential use in the development of nucleic acid-based drugs, antiviral agents, and as a tool in biochemistry research. Its structural features make it a promising candidate for further studies in drug development and medicinal chemistry.

36817-69-3

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36817-69-3 Usage

Uses

Used in Pharmaceutical Industry:
(R)-9-(1-methyl-2-hydroxyethyl)adeninde is used as a pharmaceutical compound for its potential role in the development of nucleic acid-based drugs and antiviral agents. Its unique structural features contribute to its potential as a therapeutic agent.
Used in Biochemistry Research:
(R)-9-(1-methyl-2-hydroxyethyl)adeninde is used as a research tool in biochemistry for studying the interactions and mechanisms of adenine nucleosides, which can lead to a better understanding of their biological activities and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 36817-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,1 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36817-69:
(7*3)+(6*6)+(5*8)+(4*1)+(3*7)+(2*6)+(1*9)=143
143 % 10 = 3
So 36817-69-3 is a valid CAS Registry Number.

36817-69-3Downstream Products

36817-69-3Relevant academic research and scientific papers

Synthesis of acyclic nucleoside and nucleotide analogues from amino acids: A convenient approach to a PMEA-PMPA hybrid

Jeffery, Arlen L.,Kim, Jae-Hun,Wiemer, David F.

, p. 5077 - 5083 (2000)

Nonracemic amino alcohols derived from common amino acids have been used to assemble acyclic nucleoside and nucleotide analogues with control of absolute stereochemistry. Both (R)- and (S)-2-amino-1-propanol, readily available from D- or L-alanine, were used to prepare the nucleoside analogues (R)- and (S)-9-[1- methyl-2-hydroxyethyl]adenine, and then the nucleotide analogues (R)- and (S)-9-[1-methyl-2-phosphonomethoxyethyl]adenine. In a similar fashion, the CBz derivative of L-threonine was used to prepare first (1R,2R)-9-[1-hydroxymethyl-2-hydroxypropyl]adenine, and then the bis phosphonomethoxy derivative. The bis phosphonate derived from threonine represents a unique structural hybrid of PMEA and PMPA, both of which have well established antiviral activity. (C) 2000 Elsevier Science Ltd.

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