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CAS 51549-54-3

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Adenosine, N-benzoyl-2′-deoxy-, 3′-benzoate

Description:
Adenosine, N-benzoyl-2′-deoxy-, 3′-benzoate, with the CAS number 51549-54-3, is a modified nucleoside derivative of adenosine. This compound features a benzoyl group at the nitrogen position of the ribose sugar and a benzoate moiety at the 3′ position, which enhances its lipophilicity and may influence its biological activity. It is typically characterized by its molecular structure, which includes a purine base (adenine) linked to a sugar (deoxyribose) and functional groups that can participate in various chemical reactions. The presence of aromatic rings in the benzoyl and benzoate groups can contribute to its stability and solubility properties. This compound may exhibit pharmacological activities, potentially acting as a modulator of adenosine receptors, which are involved in numerous physiological processes. Its synthesis and characterization are of interest in medicinal chemistry, particularly in the development of therapeutic agents targeting adenosine-related pathways. As with many nucleoside derivatives, it may also be studied for its potential applications in drug design and delivery systems.
Formula:C24H21N5O5
InChI:InChI=1/C24H21N5O5/c30-12-18-17(34-24(32)16-9-5-2-6-10-16)11-19(33-18)29-14-27-20-21(25-13-26-22(20)29)28-23(31)15-7-3-1-4-8-15/h1-10,13-14,17-19,30H,11-12H2,(H,25,26,28,31)/t17-,18+,19+/m0/s1
InChI key:InChIKey=GRASBJRYLQJMMU-IPMKNSEASA-N
SMILES:N(C(=O)C1=CC=CC=C1)C2=C3C(N(C=N3)[C@H]4C[C@H](OC(=O)C5=CC=CC=C5)[C@@H](CO)O4)=NC=N2
Synonyms:
  • Adenosine, N-benzoyl-2′-deoxy-, 3′-benzoate
  • N,O<sup>3′</sup>-Dibenzoyldeoxyadenosine
  • N-Benzoyl-2'-deoxyadenosine 3'-benzoate
  • N-benzoyl-3'-O-benzoyl-2'-deoxyadenosine
  • N,O3′-Dibenzoyldeoxyadenosine
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