130449-61-5

Upstream product

• 130427-54-2 2-(acetylamino)-6-<(diphenylcarbamoyl)oxy>-9-<<2-phenylselenyl)ethoxy>methyl>purine 
• 130427-55-3 C₂₉H₂₆N₆O₅Se 
• 146558-05-6 2-N-acetyl-6-O-(diphenylcarbamoyl)guanine 
• 112233-74-6 N₂-acetyl-O₆-(diphenylcarbamoyl)guanine 

Downstream Products

• 130427-56-4 Diphenyl-carbamic acid 2-acetylamino-9-oxiranyloxymethyl-9H-purin-6-yl ester 
• 130449-62-6 2-(acetylamino)-6-<(diphenylcarbamoyl)oxy>-9-<<2-hydroxy-1-<(dimethoxyphosphinyl)methoxy>ethoxy>methyl>purine 

Relevant academic research and scientific papers

A New Class of Acyclic Phosphonate Nucleotide Analogues: Phosphonate Isosteres of Acyclovir and Ganciclovir Monophosphates as Antiviral Agents

Novel pohosphonate isosteres of acyclovir (ACV) and ganciclovir (DHPG) monophosphates (20 and 32) wre foudnd to be potent and selective antiherpesvirus agents.In the series of phosphonate analogues of ACV monophosphate, only the guanine analogue 20 exhibited activity against herpesviruses, similar to the structure-activity relationship observed for base modification of ACV analogues.The phosphonate isostere of ACV monophosphate (20) was more effective than ACV in the HSV-1 infected mouse model.The 3'-carba analogues of 9-purines/pyrimidines (adenine, HPMPA; guanine, HPMPG; cytosine, HPMPC) are devoid of antiherpesvirus activity.This result confirms that the β-oxygen atom of the phosphonomethyl ether functionality in HPMP-purines/pyrimidines plays a critical role for activity against herpesviruses.

Synthesis of a phosphonate isostere of ganciclovir monophosphate: A highly cytomegalovirus active phosphonate nucleotide analogue

A novel synthetic methodology for the hydroxymethyl substituted acyclic acetal functionality was developed. The rationally designed phosphonate analogue 3 of ganciclovir monophosphate was highly active against human cytomegalovirus.