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CAS 13389-10-1

:

Adenosine, 2′-deoxy-8-(methylamino)-

Description:
Adenosine, 2′-deoxy-8-(methylamino)-, also known by its CAS number 13389-10-1, is a modified nucleoside that features a deoxyribose sugar moiety linked to an adenine base with a methylamino group at the 8-position. This compound is characterized by its structural components, which include a five-carbon sugar (deoxyribose) and a purine base (adenine). The presence of the methylamino group introduces unique chemical properties, potentially influencing its biological activity and interactions. This modification can affect the molecule's solubility, stability, and affinity for various biological targets, making it of interest in biochemical and pharmacological research. The compound may play a role in nucleic acid synthesis or serve as a precursor in the synthesis of other biologically relevant molecules. Its characteristics, such as molecular weight, melting point, and solubility, are essential for understanding its behavior in biological systems and potential applications in drug development or molecular biology.
Formula:C11H16N6O3
InChI:InChI=1S/C11H16N6O3/c1-13-11-16-8-9(12)14-4-15-10(8)17(11)7-2-5(19)6(3-18)20-7/h4-7,18-19H,2-3H2,1H3,(H,13,16)(H2,12,14,15)/t5-,6+,7+/m0/s1
InChI key:InChIKey=QPKHFQHVYJMSQB-RRKCRQDMSA-N
SMILES:N(C)C=1N(C=2C(N1)=C(N)N=CN2)[C@@H]3O[C@H](CO)[C@@H](O)C3
Synonyms:
  • Adenosine, 2′-deoxy-8-(methylamino)-
  • 9H-Purine, 6-amino-9-(2-deoxy-β-D-erythro-pentofuranosyl)-8-(methylamino)-
  • NSC 101163
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Found 2 products.
  • 2'-Deoxy-8-methylamino-adenosine
    Targetmol
    + Info

    2'-Deoxy-8-methylamino-adenosine

    CAS:
    <p>Nucleoside Derivatives - 8-Modified purine nucleosides; N-Methylated nucleosides</p>
    Formula:C11H16N6O3
    Color and Shape:Solid
    Molecular weight:280.28

    Ref: TM-TNU1234

  • 2’-Deoxy-8-methylaminoadenosine
    Biosynth
    + Info

    2’-Deoxy-8-methylaminoadenosine

    CAS:
    <p>2’-Deoxy-8-methylaminoadenosine is a nucleoside analogue that has antiviral and anticancer activities. It is synthesized by the reaction of 2’-deoxyadenosine with methylamine, which produces an N,N-dimethylated adenosine derivative. This product has been shown to be an inhibitor of RNA synthesis in human cells and animal models. The mechanism of action is thought to be similar to that of other nucleoside analogues, which are believed to exert their anticancer effects by interfering with DNA replication and cell division.</p>
    Purity:Min. 95%

    Ref: 3D-ND163127

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