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CAS 122654-31-3

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Adenosine, 2-chloro-3′-deoxy-3′-fluoro-N-methyl-

Description:
Adenosine, 2-chloro-3′-deoxy-3′-fluoro-N-methyl- is a modified nucleoside that features alterations to the adenosine structure, specifically at the 2 and 3' positions of the ribose sugar. The presence of chlorine and fluorine substituents introduces unique chemical properties, potentially affecting its biological activity and interaction with nucleic acid targets. This compound is characterized by its ability to mimic natural nucleosides, which may influence its role in biochemical pathways, particularly in relation to nucleic acid synthesis and cellular signaling. The N-methyl group enhances lipophilicity, potentially improving membrane permeability. As a synthetic analog, it may be of interest in pharmaceutical research, particularly in the development of antiviral or anticancer agents. Its CAS number, 122654-31-3, allows for precise identification and retrieval of information regarding its synthesis, properties, and applications in scientific literature. Overall, this compound exemplifies the modifications that can be made to nucleosides to explore their functional roles in biological systems.
Formula:C11H13ClFN5O3
InChI:InChI=1S/C11H13ClFN5O3/c1-14-8-6-9(17-11(12)16-8)18(3-15-6)10-7(20)5(13)4(2-19)21-10/h3-5,7,10,19-20H,2H2,1H3,(H,14,16,17)/t4-,5-,7-,10-/m1/s1
InChI key:InChIKey=DUOQYMIAHQYRQT-QYYRPYCUSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(NC)N=C(Cl)N3)O[C@H](CO)[C@H]1F
Synonyms:
  • Adenosine, 2-chloro-3′-deoxy-3′-fluoro-N-methyl-
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