Literature DB >> 1323678

Synthesis and antiviral activity of methyl derivatives of 9-[2-(phosphonomethoxy)ethyl]guanine.

K L Yu1, J J Bronson, H Yang, A Patick, M Alam, V Brankovan, R Datema, M J Hitchcock, J C Martin.   

Abstract

A number of methyl derivatives of 9-[2-(phosphonomethoxy)ethyl]guanine (PMEG, 1) have been synthesized and tested in vitro for anti-herpes and anti-human immunodeficiency virus (HIV) activity. Among these analogues, (R)-2'-methyl-PMEG [(R)-3] and 2',2'-dimethyl-PMEG (7) demonstrated potent anti-HIV activity in the XTT assay with EC50 values of 1.0 and 2.6 microM, respectively. The corresponding (S)-2'-methyl-PMEG [(S)-3] was found to be less potent against HIV. In addition, the (R) and (S) enantiomers of 9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine (HPMPG, 8) were prepared for comparison of biological activity, and shown to be active and equipotent against herpesviruses, but inactive against HIV.

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Year:  1992        PMID: 1323678     DOI: 10.1021/jm00094a005

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  5 in total

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Journal:  ACS Med Chem Lett       Date:  2020-06-24       Impact factor: 4.345

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Journal:  Antivir Chem Chemother       Date:  2018 Jan-Dec

4.  Selected Thoughts on Hydrophobicity in Drug Design.

Authors:  Lillian L Lou; John C Martin
Journal:  Molecules       Date:  2021-02-07       Impact factor: 4.411

5.  Diisopropyl {[(R)-2-(2-amino-6-chloro-9H-purin-9-yl)-1-methyl-eth-oxy]meth-yl}-phospho-nate.

Authors:  Guobao Zhao; Xinhua He; Bohua Zhong
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-03-03
  5 in total

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