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- Publications
- Influence
Acyclic nucleoside phosphonates: a key class of antiviral drugs
Almost 20 years after the broad antiviral activity spectrum of the first acyclic nucleoside phosphonates was described, several of these compounds have become important therapies for DNA virus and… Expand
A novel selective broad-spectrum anti-DNA virus agent
- E. Clercq, A. Holý, I. Rosenberg, T. Sakuma, J. Balzarini, P. C. Maudgal
- Biology, Medicine
- Nature
- 2 October 1986
A new compound has been found, (S)-9-(3-hydroxy-2-phosphonyl-methoxypropyl)adenine ((S)-HPMPA), that has potent and selective activity against a broad spectrum of DNA viruses, including herpes… Expand
Regulation of ribosomal RNA promoters with a synthetic lac operator.
- J. Brosius, A. Holý
- Biology, Medicine
- Proceedings of the National Academy of Sciences…
- 1 November 1984
A synthetic 21-base-pair long DNA fragment containing the central lac operator sequence has been inserted near the initiation point of the cloned Escherichia coli rrnB rRNA promoter P2 in the natural… Expand
Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo antiretrovirus activities of…
- J. Balzarini, A. Holý, +4 authors E. de Clercq
- Biology, Medicine
- Antimicrobial Agents and Chemotherapy
- 1 February 1993
The (S)- and (R)-enantiomers of acyclic purine nucleoside phosphonate analogs (i.e., 3-hydroxy-2-phosphonomethoxypropyl [HPMP] derivatives, 3-fluoro-2-phosphonomethoxypropyl [FPMP] derivatives, and… Expand
Antiviral activity of phosphonylmethoxyalkyl derivatives of purine and pyrimidines.
- E. De Clercq, T. Sakuma, +4 authors A. Holý
- Biology, Medicine
- Antiviral research
- 1 December 1987
Various 3-hydroxy-2-phosphonylmethoxypropyl (HPMP) and 2-phosphonylmethoxyethyl (PME) derivatives of purine [adenine (A), guanine (G), 2,6-diaminopurine (DAP), 2-monoaminopurine (MAP), hypoxanthine… Expand
(S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine, a potent and selective inhibitor of human cytomegalovirus replication.
- R. Snoeck, T. Sakuma, E. de Clercq, I. Rosenberg, A. Holý
- Chemistry, Medicine
- Antimicrobial Agents and Chemotherapy
- 1 December 1988
From a series of phosphonylmethoxyalkylpurine and -pyrimidine derivatives, (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine [(S)-HPMPC] emerged as a particularly potent and selective inhibitor of… Expand
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) effectively inhibits retrovirus replication in vitro and simian immunodeficiency virus infection in rhesus monkeys.
- J. Balzarini, L. Naesens, +5 authors E. de Clercq
- Biology, Medicine
- AIDS
- 1991
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) is a potent and selective inhibitor of the in vitro replication of a number of retroviruses, including HIV-1 and HIV-2, simian immunodeficiency virus (SIV),… Expand
Phosphonomethoxyalkyl analogs of nucleotides.
- A. Holý
- Biology, Medicine
- Current pharmaceutical design
- 30 November 2003
Acyclic nucleoside phosphonates (ANP) are analogs of nucleotides exhibiting various biological (e.g. antiviral, cytostatic, antiparasitic, immunomodulatory) activities. This review describes… Expand
Antiretrovirus Activity of a Novel Class of Acyclic Pyrimidine Nucleoside Phosphonates
- J. Balzarini, C. Pannecouque, +4 authors A. Holý
- Biology, Medicine
- Antimicrobial Agents and Chemotherapy
- 1 July 2002
ABSTRACT A novel class of acyclic nucleoside phosphonates has been discovered in which the base consists of a pyrimidine preferably containing an amino group at C-2 and C-4 and a… Expand
Efficacy of phosphonylmethoxyalkyl derivatives of adenine in experimental herpes simplex virus and vaccinia virus infections in vivo.
- E. De Clercq, A. Holý, I. Rosenberg
- Biology, Medicine
- Antimicrobial Agents and Chemotherapy
- 1 February 1989
The phosphonylmethoxyalkyl derivatives (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)adenine [(S)-HPMPA], 9-(2-phosphonylmethoxyethyl)adenine (PMEA), and 9-(2-phosphonylmethoxyethyl)-2,6-diaminopurine… Expand