Open AccessAlkoxyalkyl Esters of ( S )-9-[3-Hydroxy-2-(Phosphonomethoxy)Propyl]Adenine Are Potent Inhibitors of the Replication of Wild-Type and Drug-Resistant Human Immunodeficiency Virus Type 1 In Vitro
Author(s) -
Karl Y. Hostetler,
Kathy A. Aldern,
William Wan,
Stephanie L. Ciesla,
James R. Beadle
Publication year - 2006
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01223-05
Subject(s) - virology , biology , resistance mutation , virus , reverse transcriptase , mutation , herpes simplex virus , genetics , polymerase chain reaction , gene
(S )-9-[3-Hydroxy-2-(phosphonomethoxy)propyl]adenine [(S )-HPMPA], is an effective broad-spectrum antiviral against many DNA viruses but has been reported to be inactive against human immunodeficiency virus (HIV). We synthesized several alkoxyalkyl esters of (S )-HPMPA and now report that hexadecyloxypropyl-(S )-HPMPA [HDP-(S )-HPMPA] and octadecyloxyethyl-(S )-HPMPA [ODE-(S )-HPMPA]had 50% effective concentrations of 0.4 to 7.0 nanomolar and were nearly fully active against HIV variants having reverse transcriptase mutations M184V and K103N and against a zidovudine-resistant variant with mutations D67N, K70R, T215Y, and K219Q. Resistance to HDP-(S )-HPMPA and ODE-(S )-HPMPA was noted for a mutant with mutation K65R. HDP-(S )-HPMPA is also active against herpes simplex virus type 1, human cytomegalovirus, hepatitis B virus, adenoviruses, and orthopoxviruses and is worthy of further evaluation as a possibly therapy for HIV infection.