172529-94-1Relevant articles and documents
Virtual Screening of Acyclovir Derivatives as Potential Antiviral Agents: Design, Synthesis, and Biological Evaluation of New Acyclic Nucleoside ProTides
Derudas, Marco,Vanpouille, Christophe,Carta, Davide,Zicari, Sonia,Andrei, Graciela,Snoeck, Robert,Brancale, Andrea,Margolis, Leonid,Balzarini, Jan,McGuigan, Christopher
, p. 7876 - 7896 (2017)
Following our findings on the anti-human immunodeficiency virus (HIV) activity of acyclovir (ACV) phosphate prodrugs, we herein report the ProTide approach applied to a series of acyclic nucleosides aimed at the identification of novel and selective antiv
The synthesis of a new probe for PET imaging reporter gene HSV1-tk: 2-Amino-6-[18F] fluoro-9- (4-hydroxy-3-hydroxymethylbutyl) purine (6-[18F]fluoropenciclovir)
Cai, Hancheng,Yin, Duanzhi,Zhang, Lan,Wang, Yongxian
, p. 653 - 661 (2006)
The one step radiosynthesis of 2-amino-6- [18F]fluoro-9-(4- hydroxy-3-hydroxymethyl-butyl) purine (6-[18F]fluoropenciclovir) 6 is reported. Radiolabeled product 6-[18F]fluoropenciclovir 6 was prepared by radiofluorination of compound 4 with [18F]KF and isolated by a silica Sep-Pak cartridge. The radiochemical yield of compound 6 was 45-55% decay corrected (d.c.) in six runs with radiochemical purity >98% and the radiosynthesis time was 35-42 min from end of bombardment (EOB). Copyright
Preparation of famciclovir and other purine derivatives
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Page/Page column 4; 5, (2008/06/13)
Purine derivatives, substituted at the 9-position, are prepared from a chloro substituted purine starting material, first making an alkyl substitution at the 9-position, then forming the desired esterified side chain, reducing this and hydrogenating the resultant diol prior to addition of alkyl carbonyl groups.