CAS 7387-58-8
:N-acetyl-9-(2,3,5-tri-O-acetylpentofuranosyl)-9H-purin-6-amine
Description:
N-acetyl-9-(2,3,5-tri-O-acetylpentofuranosyl)-9H-purin-6-amine, with the CAS number 7387-58-8, is a purine derivative characterized by its complex structure that includes a purine base and a sugar moiety. This compound features an N-acetyl group at the 9-position of the purine ring, which contributes to its solubility and biological activity. The presence of the 2,3,5-tri-O-acetylpentofuranosyl group indicates that it is a glycosylated compound, enhancing its stability and potential interactions with biological targets. The acetyl groups on the sugar enhance lipophilicity, which can influence its pharmacokinetic properties. This compound is of interest in biochemical research, particularly in the study of nucleosides and their analogs, which play crucial roles in cellular processes such as energy transfer and signal transduction. Its unique structural features may also provide insights into the design of antiviral or anticancer agents, making it a valuable subject of study in medicinal chemistry.
Formula:C18H21N5O8
InChI:InChI=1/C18H21N5O8/c1-8(24)22-16-13-17(20-6-19-16)23(7-21-13)18-15(30-11(4)27)14(29-10(3)26)12(31-18)5-28-9(2)25/h6-7,12,14-15,18H,5H2,1-4H3,(H,19,20,22,24)
SMILES:CC(=Nc1c2c(ncn1)n(cn2)C1C(C(C(COC(=O)C)O1)OC(=O)C)OC(=O)C)O
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