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CAS 3413-67-0

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Adenosine, 2′-deoxy-1,6-dihydro-1-methyl-

Description:
Adenosine, 2′-deoxy-1,6-dihydro-1-methyl- (CAS 3413-67-0) is a nucleoside derivative that plays a significant role in biochemistry, particularly in the context of nucleic acid metabolism. This compound features a purine base, adenine, linked to a deoxyribose sugar, which is characteristic of deoxynucleosides. The presence of a methyl group at the 1-position and the saturation of the 1,6-bonded carbon atoms contribute to its unique structural properties. This modification can influence its biological activity and interactions with enzymes and receptors. The compound is soluble in water and exhibits stability under physiological conditions, making it relevant for various biochemical applications, including studies on DNA synthesis and repair. Additionally, it may serve as a substrate or inhibitor in enzymatic reactions involving nucleotides. Its structural characteristics and modifications can also provide insights into the design of nucleoside analogs for therapeutic purposes. Overall, this compound is an important molecule in the field of molecular biology and medicinal chemistry.
Formula:C11H17N5O3
InChI:InChI=1S/C11H17N5O3/c1-15-4-14-11-9(10(15)12)13-5-16(11)8-2-6(18)7(3-17)19-8/h4-8,10,17-18H,2-3,12H2,1H3/t6-,7+,8+,10?/m0/s1
InChI key:InChIKey=GYVCSXZSBPEFAO-ZYPUDGPYSA-N
SMILES:NC1C2=C(N(C=N2)[C@@H]3O[C@H](CO)[C@@H](O)C3)N=CN1C
Synonyms:
  • Adenosine, 2′-deoxy-1,6-dihydro-1-methyl-
  • (2R,3S,4R,5S)-3,4-Di-O-Isopropylidene-2-methyl-1-nonyl-3,4,5-piperidinetriol
  • 2'- Deoxy- 1, 6- dihydro- 1- methyladenosine
  • Adenosine, 2'-deoxy-1,6-dihydro-1-methyl- (9CI)
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  • 2'- Deoxy- 1, 6- dihydro- 1- methyladenosine
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    2'- Deoxy- 1, 6- dihydro- 1- methyladenosine

    CAS:
    <p>2'- Deoxy- 1, 6- dihydro- 1- methyladenosine is a novel nucleoside activator. It is a modified form of adenosine and has shown anticancer activity in vivo. This compound also has antiviral activity against herpes simplex virus type 2 (HSV-2) and human cytomegalovirus (CMV). The antiviral effect of this drug is due to its ability to penetrate the cell membrane and inhibit viral DNA synthesis by inhibiting deoxyribonucleoside triphosphate (dNTP) incorporation into the viral DNA strand.</p>
    Formula:C11H17N5O3
    Purity:Min. 95%
    Molecular weight:267.28 g/mol

    Ref: 3D-ND170656

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