Development of CMX001 for the treatment of poxvirus infections

R Lanier, L Trost, T Tippin, B Lampert, A Robertson… - Viruses, 2010 - mdpi.com
CMX001 (phosphonic acid,[[(S)-2-(4-amino-2-oxo-1 (2H)-pyrimidinyl)-1-(hydroxymethyl)
ethoxy] methyl] mono [3-(hexadecyloxy) propyl] ester) is a lipid conjugate of the acyclic …

Efficacy of CMX001 as a prophylactic and presymptomatic antiviral agent in New Zealand white rabbits infected with rabbitpox virus, a model for orthopoxvirus …

AD Rice, MM Adams, B Lampert, S Foster, R Lanier… - Viruses, 2011 - mdpi.com
CMX001, a lipophilic nucleotide analog formed by covalently linking 3-(hexdecyloxy) propan-
1-ol to cidofovir (CDV), is being developed as a treatment for smallpox. CMX001 has …

Synthesis and early development of hexadecyloxypropyl-cidofovir: an oral antipoxvirus nucleoside phosphonate

KY Hostetler - Viruses, 2010 - mdpi.com
Hexadecyloxypropyl-cidofovir (HDP-CDV) is a novel ether lipid conjugate of (S)-1-(3-
hydroxy-2-phosphonoylmethoxypropyl)-cytosine (CDV) which exhibits a remarkable …

Efficacy of therapeutic intervention with an oral ether–lipid analogue of cidofovir (CMX001) in a lethal mousepox model

S Parker, E Touchette, C Oberle, M Almond… - Antiviral research, 2008 - Elsevier
In the 21st century we are faced with the potential use of natural or recombinant VARV and
MPXV as biological weapons, and the emergence of human MPXV. Such an occurrences …

Efficacy of CMX001 as a post exposure antiviral in New Zealand White rabbits infected with rabbitpox virus, a model for orthopoxvirus infections of humans

AD Rice, MM Adams, G Wallace, AM Burrage… - Viruses, 2011 - mdpi.com
CMX001, a lipophilic nucleotide analog formed by covalently linking 3-(hexdecyloxy) propan-
1-ol to cidofovir (CDV), is being developed as a treatment for smallpox. In the absence of …

Cidofovir activity against poxvirus infections

G Andrei, R Snoeck - Viruses, 2010 - mdpi.com
Cidofovir [(S)-1-(3-hydroxy-2-phosphonylmethoxypropyl) cytosine, HPMPC] is an acyclic
nucleoside analog approved since 1996 for clinical use in the treatment of cytomegalovirus …

Selection and recombinant phenotyping of a novel CMX001 and cidofovir resistance mutation in human cytomegalovirus

SH James, NB Price, CB Hartline… - Antimicrobial agents …, 2013 - Am Soc Microbiol
ABSTRACT CMX001 is an orally available lipid acyclic nucleotide phosphonate that delivers
high intracellular levels of cidofovir (CDV)-diphosphate and exhibits enhanced in vitro …

Cidofovir in the therapy and short-term prophylaxis of poxvirus infections

E De Clercq - Trends in Pharmacological Sciences, 2002 - cell.com
Although it is often stated that only vaccination would be able to contain or protect the
population against a catastrophic smallpox outbreak, the acyclic nucleoside phosphonate …

Progress in the discovery of compounds inhibiting orthopoxviruses in animal models

DF Smee - Antiviral Chemistry and Chemotherapy, 2008 - journals.sagepub.com
Surrogate animal models must be used for testing antiviral agents against variola (smallpox)
virus infections. Once developed, these compounds can be stockpiled for use in the event of …

[HTML][HTML] Efficacy of oral active ether lipid analogs of cidofovir in a lethal mousepox model

RM Buller, G Owens, J Schriewer, L Melman… - Virology, 2004 - Elsevier
Cidofovir (CDV) is a highly effective inhibitor of orthopoxvirus replication and may be used
intravenously to treat smallpox or complications arising from the smallpox vaccine under an …