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CAS 4546-54-7

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2-Aminopurine riboside

Description:
2-Aminopurine riboside is a purine nucleoside that consists of a ribose sugar linked to the purine base 2-aminopurine. This compound is characterized by its structural features, which include an amino group at the 2-position of the purine ring, distinguishing it from adenine. It is known for its role as a nucleoside analog and has been studied for its potential applications in molecular biology and biochemistry, particularly in the context of nucleic acid research and as a tool for studying RNA and DNA processes. 2-Aminopurine riboside can act as a mutagen and is often used in research to induce mutations in various organisms. Its solubility in water and ability to incorporate into nucleic acids make it a valuable compound in experimental settings. Additionally, it may exhibit biological activity, influencing cellular processes and gene expression. As with many nucleosides, its stability and reactivity can be influenced by environmental conditions, making it important to handle and store it properly in laboratory settings.
Formula:C10H13N5O4
InChI:InChI=1/C10H13N5O4/c11-10-12-1-4-8(14-10)15(3-13-4)9-7(18)6(17)5(2-16)19-9/h1,3,5-7,9,16-18H,2H2,(H2,11,12,14)
InChI key:InChIKey=JVOJULURLCZUDE-JXOAFFINSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=CN=C(N)N3)O[C@H](CO)[C@H]1O
Synonyms:
  • 2-Amino-9-β-<span class="text-smallcaps">D</span>-ribofuranosylpurine
  • 2-Aminonebularine
  • 2-Aminopurine ribonucleoside
  • 9-pentofuranosyl-9H-purin-2-amine
  • 9-β-<span class="text-smallcaps">D</span>-Ribofuranosyl-9H-purin-2-amine
  • 9H-Purin-2-amine, 9-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
  • 9H-Purine, 2-amino-9-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
  • NSC 36906
  • 2-Aminopurine riboside
  • 9H-Purin-2-amine, 9-β-D-ribofuranosyl-
  • See more synonyms
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