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CAS 103213-52-1

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3H-Imidazo[2,1-i]purine, 3-[5-O-[hydroxy(phosphonooxy)phosphinyl]-β-D-ribofuranosyl]-, disodium salt

Description:
3H-Imidazo[2,1-i]purine, 3-[5-O-[hydroxy(phosphonooxy)phosphinyl]-β-D-ribofuranosyl]-, disodium salt, commonly referred to as a nucleotide analogue, exhibits several notable characteristics. This compound is a derivative of purine, featuring an imidazole ring fused to a pyrimidine structure, which is essential for its biological activity. The presence of a ribofuranosyl moiety indicates its role in nucleic acid metabolism, potentially influencing RNA synthesis and function. The disodium salt form enhances its solubility in aqueous solutions, making it more bioavailable for pharmacological applications. Its phosphonyl group suggests potential interactions with enzymes involved in nucleotide metabolism, possibly acting as an inhibitor or modulator. This compound is of interest in medicinal chemistry and biochemistry, particularly in the development of antiviral or anticancer agents, due to its structural similarity to natural nucleotides. Overall, its unique structural features and functional groups contribute to its potential therapeutic applications and biological significance.
Formula:C12H15N5O10P2·2Na
InChI:InChI=1S/C12H15N5O10P2.2Na/c18-8-6(3-25-29(23,24)27-28(20,21)22)26-12(9(8)19)17-5-14-7-10-13-1-2-16(10)4-15-11(7)17;;/h1-2,4-6,8-9,12,18-19H,3H2,(H,23,24)(H2,20,21,22);;/t6-,8-,9-,12-;;/m1../s1
InChI key:InChIKey=NFQPKDAZPRNUNF-CMUBXXRSSA-N
SMILES:O[C@H]1[C@H](N2C3=C(C=4N(C=N3)C=CN4)N=C2)O[C@H](COP(OP(=O)(O)O)(=O)O)[C@H]1O.[Na]
Synonyms:
  • 3H-Imidazo[2,1-i]purine, 3-[5-O-[hydroxy(phosphonooxy)phosphinyl]-β-D-ribofuranosyl]-, disodium salt
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