CAS 35665-58-8
:9-(2-deoxypentofuranosyl)-N,N-dimethyl-9H-purin-6-amine
Description:
9-(2-Deoxypentofuranosyl)-N,N-dimethyl-9H-purin-6-amine, commonly known as a derivative of purine, is a nucleoside analog characterized by its structural components, which include a purine base and a sugar moiety. This compound features a 2-deoxypentofuranosyl sugar, which is a five-carbon sugar lacking an oxygen atom at the second carbon, making it a crucial component of DNA. The presence of two dimethyl groups attached to the nitrogen atoms in the purine structure enhances its lipophilicity and may influence its biological activity. This compound is of interest in biochemical research, particularly in the study of nucleic acids and their analogs, as it may exhibit properties relevant to antiviral or anticancer activities. Its CAS number, 35665-58-8, allows for precise identification in chemical databases. Overall, the unique combination of its purine base and sugar structure contributes to its potential applications in medicinal chemistry and molecular biology.
Formula:C12H17N5O3
InChI:InChI=1/C12H17N5O3/c1-16(2)11-10-12(14-5-13-11)17(6-15-10)9-3-7(19)8(4-18)20-9/h5-9,18-19H,3-4H2,1-2H3
SMILES:CN(C)c1c2c(ncn1)n(cn2)C1CC(C(CO)O1)O
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Found 3 products.
2'-Deoxy-N6,N6-dimethyladenosine
CAS:<p>2'-Deoxy-N6,N6-dimethyladenosine is a Nucleoside Derivative - 6-Modified purine nucleoside.</p>Formula:C12H17N5O3Color and Shape:SolidMolecular weight:279.3N6-Dimethyldeoxyadenosine
CAS:Controlled ProductFormula:C12H17N5O3Color and Shape:NeatMolecular weight:279.2952'-Deoxy- N, N- dimethyl-adenosine
CAS:<p>2'-Deoxy-N, N-Dimethyl-Adenosine is a nucleoside that is phosphorylated to 2'-deoxy-N, N-dimethyl-adenosyl monophosphate. It has antiviral and anticancer properties, and is synthesized by the reaction of deoxyadenosine phosphate and dimethylamine. This product is a novel nucleoside with modified phosphate groups. The synthesis of this nucleoside has been patented.</p>Formula:C12H17N5O3Purity:Min. 95%Molecular weight:279.3 g/mol


