Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2002 Apr;46(4):991-5.
doi: 10.1128/AAC.46.4.991-995.2002.

Enhanced inhibition of orthopoxvirus replication in vitro by alkoxyalkyl esters of cidofovir and cyclic cidofovir

Affiliations

Enhanced inhibition of orthopoxvirus replication in vitro by alkoxyalkyl esters of cidofovir and cyclic cidofovir

Earl R Kern et al. Antimicrob Agents Chemother. 2002 Apr.

Abstract

The nucleotide phosphonates cidofovir (CDV) and cyclic cidofovir (cCDV) are potent antiviral compounds when administered parenterally but are not well absorbed orally. These compounds have been reported to have activity against orthopoxvirus replication in vitro and in animal models when administered parenterally or by aerosol. To obtain better oral activity, we synthesized a novel series of analogs of CDV and cCDV by esterification with two long-chain alkoxyalkanols, 3-hexadecyloxy-1-propanol (HDP-CDV; HDP-cCDV) or 3-octadecyloxy-1-ethanol (ODE-CDV; ODE-cCDV). Their activities were evaluated and compared with those of CDV and cCDV in human foreskin fibroblast (HFF) cells infected with vaccinia virus (VV) or cowpox virus (CV) using a plaque reduction assay. The 50% effective concentrations (EC(50)s) against VV in HFF cells for CDV and cCDV were 46.2 and 50.6 microM compared with 0.84 and 3.8 microM for HDP-CDV and HDP-cCDV, respectively. The EC(50)s for ODE-CDV and ODE-cCDV were 0.20 and 1.1 microM, respectively. The HDP analogs were 57- and 13-fold more active than the parent nucleotides, whereas the ODE analogs were 231- and 46-fold more active than the unmodified CDV and cCDV. Similar results were obtained using CV. Cytotoxicity studies indicated that although the analogs were more toxic than the parent nucleotides, the selective index was increased by 4- to 13-fold. These results indicate that the alkoxyalkyl esters of CDV and cCDV have enhanced activity in vitro and need to be evaluated for their oral absorption and efficacy in animal models.

PubMed Disclaimer

Figures

FIG. 1.
FIG. 1.
Synthesis and structures of alkoxyalkyl analogs of CDV and cCDV. The arrows indicate the following reagents: (a) N,N-dicyclohexyl-morpholinocarboxamide, N,N-dicyclohexylcarbodiimide, pyridine, 100°C; (b) 1-bromo-3-octadecyloxyethane (ODE), or 1-bromo-3-hexadecyloxypropane (HDP), N,N-dimethylformamide, 80°C; (c) 0.5 M NaOH. The numbers in parentheses are the compound numbers (see the text).

Similar articles

Cited by

References

    1. Bischofberger, N., M. J. M. Hitchcock, M. S. Chen, D. B. Barkhimer, K. C. Cundy, K. M. Kent, S. A. Lacy, W. A. Lee, Z.-H. Li, D. B. Mendel, D. F. Smee, and J. L. Smith. 1994. 1-[((s)-2-Hydroxy-2-oxo-1,4,2-dioxaphosphorinan-5-yl)methyl]cytosine, an intracellular prodrug for (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine, with improved therapeutic index in vivo. Antimicrob. Agents Chemother. 38:2387-2391. - PMC - PubMed
    1. Bray, M., M. Martinez, D. F. Smee, D. Kefauver, E. Thompson, and J. W. Huggins. 2000. Cidofovir protects mice against lethal aerosol or intranasal cowpox virus challenges. J. Infect. Dis. 181:10-19. - PubMed
    1. Breman, J. G., and D. A. Henderson. 1998. Poxvirus dilemmas--monkeypox, smallpox, and biological terrorism. N. Engl. J. Med. 339:556-559. - PubMed
    1. Collins, D. J., D. C. Quenelle, and E. R. Kern. 2001. Systemic and cutaneous infections of mice with vaccinia and cowpox viruses and efficacy of cidofovir. Antiviral Res. 50:A70. - PMC - PubMed
    1. Cundy, K. C., A. M. Bidgood, G. Lynch, J.-P. Shaw, L. Griffin, and W. A. Lee. 1996. Pharmacokinetics, bioavailability, metabolism and tissue distribution of cidofovir (HPMPC) and cyclic HPMPC in rats. Drug Metab. Disp. 24:745-752. - PubMed

Publication types

MeSH terms

LinkOut - more resources