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CAS 4338-48-1

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N6-(2-Hydroxyethyl)adenosine

Description:
N6-(2-Hydroxyethyl)adenosine is a modified nucleoside derived from adenosine, characterized by the addition of a 2-hydroxyethyl group at the nitrogen-6 position of the adenine base. This modification can influence the molecule's biological activity, stability, and interaction with various enzymes and receptors. The compound is typically soluble in water and exhibits properties similar to adenosine, such as involvement in cellular signaling and potential roles in various biochemical pathways. Its structural modification may enhance its pharmacological properties, making it of interest in research related to nucleoside analogs and their therapeutic applications. Additionally, N6-(2-Hydroxyethyl)adenosine may be studied for its effects on cellular processes, including proliferation, differentiation, and apoptosis. As with many nucleoside derivatives, its characteristics can be influenced by factors such as pH, temperature, and the presence of other ions or molecules in the environment. Overall, this compound represents a significant area of interest in medicinal chemistry and biochemistry.
Formula:C12H17N5O5
InChI:InChI=1S/C12H17N5O5/c18-2-1-13-10-7-11(15-4-14-10)17(5-16-7)12-9(21)8(20)6(3-19)22-12/h4-6,8-9,12,18-21H,1-3H2,(H,13,14,15)/t6-,8-,9-,12-/m1/s1
InChI key:InChIKey=BBOCDRLDMQHWJP-WOUKDFQISA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(NCCO)N=CN3)O[C@H](CO)[C@H]1O
Synonyms:
  • 6-Hydroxyethyladenosine
  • 6-[(2-Hydroxyethyl)amino]-9-β-<span class="text-smallcaps">D</span>-ribofuranosylpurine
  • Adenosine, N-(2-hydroxyethyl)-
  • N-(2-hydroxyethyl)-9-pentofuranosyl-9H-purin-6-amine
  • N6-(2-hydroxyethyl)adenosine
  • N<sup>6</sup>-(2-Hydroxyethyl)adenosine
  • NSC 54251
  • 6-[(2-Hydroxyethyl)amino]-9-β-D-ribofuranosylpurine
  • N-(2-Hydroxyethyl)adenosine
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