In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-beta-D-dioxolane-guanosine and suppress resistance to 3′-azido-3′deoxythymidine
Bazmi H, Hammond JL, Cavalcanti SC, Chu CK, Schinazi RF & Mellors JW (2000) In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-beta-D-dioxolane-guanosine and suppress resistance to 3′-azido-3′deoxythymidine. Antimicrobial Agents Chemotherapy 44:1783-1788.
In vitro susceptibilities of wild-type or drug-resistant hepatitis B virus to (-)-beta-D-2,6-diaminopurine dioxolane and 2′-fluoro-5-methyl-beta-L-arabinofuranosyluracil
Chin R, Shaw T, Torresi J, Sozzi V, Trautwein C, Bock T, Manns M, Isom H, Furman P & Locarnini S (2001) In vitro susceptibilities of wild-type or drug-resistant hepatitis B virus to (-)-beta-D-2,6-diaminopurine dioxolane and 2′-fluoro-5-methyl-beta-L-arabinofuranosyluracil. Antimicrobial Agents Chemotherapy 45: 2495-2501.
Mechanism of action and in vitro activity of 1′,3′-dioxolanylpurine nucleoside analogues against sensitive and drug-resistant human immunodeficiency virus type 1 variants
Gu Z, Wainberg Ma, Nguyen-Ba N, L'Heureux L, De Muys JM, Bowlin TL & Rando RF (1999) Mechanism of action and in vitro activity of 1′,3′-dioxolanylpurine nucleoside analogues against sensitive and drug-resistant human immunodeficiency virus type 1 variants. Antimicrobial Agents Chemotherapy 43:2376-2382.
Dioxolane guanosine, the active form of the prodrug diaminopurine dioxolane, is a potent inhibitor of drug-resistant HIV-1 isolates from patients for whom standard nucleoside therapy fails
Mewshaw JP, Myrick FT, Wakefield DA, Hooper BJ, Harris JL, McCreedy B & Borroto-Esoda K (2002) Dioxolane guanosine, the active form of the prodrug diaminopurine dioxolane, is a potent inhibitor of drug-resistant HIV-1 isolates from patients for whom standard nucleoside therapy fails. Journal of Acquired Immune Deficiency Syndromes 29:11-20.
Inhibitory activity of dioxolane purine analogues on wild-type and lamivudine-resistant mutants of hepadnaviruses
Seigneres B, Pichoud C, Martin P, Furman P, Trepo C & Zoulim F (2002) Inhibitory activity of dioxolane purine analogues on wild-type and lamivudine-resistant mutants of hepadnaviruses. Hepatology 36:710-722.
Inhibition of the replication of the DNA polymerase M550V mutation variant of human hepatitis B virus by adefovir, tenofovir, L-FMAU, DAPD, penciclovir and lobucavir
Ying C, De Clercq E, Nicholson W, Furman P & Neyts J (2000) Inhibition of the replication of the DNA polymerase M550V mutation variant of human hepatitis B virus by adefovir, tenofovir, L-FMAU, DAPD, penciclovir and lobucavir. Journal of Viral Hepatitis 7:161-165.