Product Name:(2R,3R,4S,5R)-2-(6-Amino-2-(phenylamino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

IUPAC Name:(2R,3R,4S,5R)-2-[6-amino-2-(phenylamino)-9H-purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol

CAS:53296-10-9
Molecular Formula:C16H18N6O4
Purity:95%
Catalog Number:CM138715
Molecular Weight:358.36

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CM138715-1g 7-8 Weeks ƴƚǫdž

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Product Details

CAS NO:53296-10-9
Molecular Formula:C16H18N6O4
Melting Point:-
Smiles Code:O[C@H]1[C@H](N2C=NC3=C(N)N=C(NC4=CC=CC=C4)N=C23)O[C@H](CO)[C@H]1O
Density:
Catalog Number:CM138715
Molecular Weight:358.36
Boiling Point:766°C at 760 mmHg
MDL No:MFCD00055119
Storage:Store at 2-8°C.

Category Infos

Nucleosides and Nucleotides
Nucleosides consist of a nucleotide and a five-carbon sugar, and a nucleotide consists of a nucleotide, a five-carbon sugar, and one or more phosphate groups.
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Nucleosides
Nucleosides are glycosylamines that can be thought of as nucleotides without a phosphate group. A nucleoside consists simply of a nucleobase (also termed a nitrogenous base) and a five-carbon sugar (ribose or 2'-deoxyribose).

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Product Other Information

Product Overview 2-Phenylaminoadenosine (2-PAA) is an important nucleoside analog that has been studied extensively in scientific research. It is a synthetic compound that is structurally similar to adenosine, a naturally occurring nucleoside. 
Synthesis Method 2-Phenylaminoadenosine can be synthesized in a number of ways, including the use of chemical synthesis, enzymatic synthesis, or biotransformation. In chemical synthesis, 2-Phenylaminoadenosine is synthesized from adenosine and a phenyl group through a series of reactions. Enzymatic synthesis involves the use of enzymes to catalyze the formation of 2-Phenylaminoadenosine from adenosine, while biotransformation involves the use of microorganisms to convert adenosine into 2-Phenylaminoadenosine.
Chemical Properties 2-Phenylaminoadenosine is a synthetic compound that is relatively easy to synthesize and store. Additionally, 2-Phenylaminoadenosine is relatively stable and has a long shelf life.
Synthesis and Application In vivo studies have utilized 2-Phenylaminoadenosine to investigate the effects of drugs on the cardiovascular system, while in vitro studies have used it to evaluate the biological activities of various drugs.
Future Directions Future studies should focus on further elucidating the mechanisms of action of 2-Phenylaminoadenosine and exploring its potential therapeutic applications. Additionally, further research should focus on the development of novel synthetic methods for the synthesis of 2-Phenylaminoadenosine, as well as the development of new analogs with improved pharmacological properties. Finally, further research should focus on the development of novel delivery methods for 2-Phenylaminoadenosine, such as nanoparticles or liposomes.