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Antiviral l-Nucleosides Specific for Hepatitis B Virus Infection

Antimicrobial Agents and Chemotherapy, 2001-01, Vol.45 (1), p.229-235

2001

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SYNTHESIS AND ANTI-HIV ACTIVITY OF NEW MODIFIED 1,2,3-TRIAZOLE ACYCLONUCLEOSIDES

Nucleosides, nucleotides & nucleic acids, 2001-01, Vol.20 (12), p.1949-1960

2001

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Combinatorially Selected Guanosine-Quartet Structure is a Potent Inhibitor of Human Immunodeficiency Virus Envelope-Mediated Cell Fusion

Proceedings of the National Academy of Sciences - PNAS, 1994-02, Vol.91 (4), p.1356-1360

1994

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Mononucleoside Phosphotriester Derivatives with S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups: Intracellular Delivery of 3'-Azido-2',3'-dideoxythymidine 5'-Monophosphate

Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.3941-3950

1995

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Pharmacology of β-l-Thymidine and β-l-2′-Deoxycytidine in HepG2 Cells and Primary Human Hepatocytes: Relevance to Chemotherapeutic Efficacy against Hepatitis B Virus

Antimicrobial Agents and Chemotherapy, 2002-06, Vol.46 (6), p.1728-1733

2002

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Anti-human immunodeficiency virus activities of the beta-L enantiomer of 2',3'-dideoxycytidine and its 5-fluoro derivative in vitro

Antimicrobial Agents and Chemotherapy, 1994-06, Vol.38 (6), p.1292-1297

1994

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SATE pronucleotide approaches: an overview

Mini reviews in medicinal chemistry, 2004-05, Vol.4 (4), p.395

2004

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New bis(SATE) prodrug of AZT 5′‐monophosphate: In vitro anti‐HIV activity, stability, and potential oral absorption

Journal of pharmaceutical sciences, 2001-04, Vol.90 (4), p.448-463

2001

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Decomposition Pathways and in Vitro HIV Inhibitory Effects of IsoddA Pronucleotides: Toward a Rational Approach for Intracellular Delivery of Nucleoside 5‘-Monophosphates

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1981-1990

1996

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Pure nucleoside enantiomers of beta-2',3'-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro

Antimicrobial Agents and Chemotherapy, 1994-09, Vol.38 (9), p.2172-2174

1994

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Comparative evaluation of seven oligonucleotide analogs as potential antisense agents

Journal of medicinal chemistry, 1993, Vol.36 (2), p.280-287

1993

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The pro-oligonucleotide approach: solid phase synthesis and preliminary evaluation of model pro-dodecathymidylates

Nucleic acids research, 1998-05, Vol.26 (9), p.2069-2074

1998

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Comparative analysis of anti-human immunodeficiency virus type 1 activities of dideoxynucleoside analogs in resting and activated peripheral blood mononuclear cells

Antimicrobial Agents and Chemotherapy, 1995-11, Vol.39 (11), p.2555-2559

1995

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In vitro inhibition of hepatitis C virus gene expression by chemically modified antisense oligodeoxynucleotides

Antimicrobial Agents and Chemotherapy, 1996-10, Vol.40 (10), p.2337-2344

1996

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Use of MALDI-TOF mass spectrometry to monitor solid-phase synthesis of oligonucleotides

Analytical and bioanalytical chemistry, 2002-09, Vol.374 (1), p.57-63

2002

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Synthesis of ( Z) and ( E) α-alkenyl phosphonic acid derivatives of purines and pyrimidines

Tetrahedron, 1998-04, Vol.54 (15), p.3807-3816

1998

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Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA BIS(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine

Biochemical pharmacology, 1994-07, Vol.48 (1), p.11-14

1994

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Inhibition of human immunodeficiency virus type 1 reverse transcriptase by the 5'-triphosphate beta enantiomers of cytidine analogs

Antimicrobial Agents and Chemotherapy, 1994-10, Vol.38 (10), p.2300-2305

1994

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Effects of nucleotide analogues on human immunodeficiency virus type 1 integrase

Molecular pharmacology, 1996-04, Vol.49 (4), p.621-628

1996

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Synthesis, Conformational Analysis, and Biological Activity of C-Thioribonucleosides Related to Tiazofurin

Journal of medicinal chemistry, 2000-04, Vol.43 (7), p.1264-1270

2000

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Nucleoside Analogues as Chemotherapeutic Agents: A Review

Nucleosides & nucleotides, 1992-02, Vol.11 (2-4), p.903-945

1992

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S-acyl-2-thioethyl (SATE) pronucleotides are potent inhibitors of HIV-1 replication in T-lymphoid cells cross-resistant to deoxycytidine and thymidine analogs

Antiviral research, 2002-02, Vol.53 (2), p.143-152

2002

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Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

Journal of medicinal chemistry, 1996-12, Vol.39 (25), p.4958-4965

1996

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Lipophilic pro-oligonucleotides are rapidly and efficiently internalized in HeLa cells

Nucleic acids research, 1999-10, Vol.27 (20), p.4071-4076

1999

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S-Acyl-2-thioethyl Aryl Phosphotriester Derivatives as Mononucleotide Prodrugs

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4570-4574

2000

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Antiviral l-Nucleosides Specific for Hepatitis B Virus Infection

SYNTHESIS AND ANTI-HIV ACTIVITY OF NEW MODIFIED 1,2,3-TRIAZOLE ACYCLONUCLEOSIDES

Combinatorially Selected Guanosine-Quartet Structure is a Potent Inhibitor of Human Immunodeficiency Virus Envelope-Mediated Cell Fusion

Mononucleoside Phosphotriester Derivatives with S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups: Intracellular Delivery of 3'-Azido-2',3'-dideoxythymidine 5'-Monophosphate

Pharmacology of β-l-Thymidine and β-l-2′-Deoxycytidine in HepG2 Cells and Primary Human Hepatocytes: Relevance to Chemotherapeutic Efficacy against Hepatitis B Virus

Anti-human immunodeficiency virus activities of the beta-L enantiomer of 2',3'-dideoxycytidine and its 5-fluoro derivative in vitro

SATE pronucleotide approaches: an overview

New bis(SATE) prodrug of AZT 5′‐monophosphate: In vitro anti‐HIV activity, stability, and potential oral absorption

Decomposition Pathways and in Vitro HIV Inhibitory Effects of IsoddA Pronucleotides: Toward a Rational Approach for Intracellular Delivery of Nucleoside 5‘-Monophosphates

Pure nucleoside enantiomers of beta-2',3'-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro

Comparative evaluation of seven oligonucleotide analogs as potential antisense agents

The pro-oligonucleotide approach: solid phase synthesis and preliminary evaluation of model pro-dodecathymidylates

Comparative analysis of anti-human immunodeficiency virus type 1 activities of dideoxynucleoside analogs in resting and activated peripheral blood mononuclear cells

In vitro inhibition of hepatitis C virus gene expression by chemically modified antisense oligodeoxynucleotides

Use of MALDI-TOF mass spectrometry to monitor solid-phase synthesis of oligonucleotides

Synthesis of ( Z) and ( E) α-alkenyl phosphonic acid derivatives of purines and pyrimidines

Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA BIS(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine

Inhibition of human immunodeficiency virus type 1 reverse transcriptase by the 5'-triphosphate beta enantiomers of cytidine analogs

Effects of nucleotide analogues on human immunodeficiency virus type 1 integrase

Synthesis, Conformational Analysis, and Biological Activity of C-Thioribonucleosides Related to Tiazofurin

Nucleoside Analogues as Chemotherapeutic Agents: A Review

S-acyl-2-thioethyl (SATE) pronucleotides are potent inhibitors of HIV-1 replication in T-lymphoid cells cross-resistant to deoxycytidine and thymidine analogs

Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

Lipophilic pro-oligonucleotides are rapidly and efficiently internalized in HeLa cells

S-Acyl-2-thioethyl Aryl Phosphotriester Derivatives as Mononucleotide Prodrugs

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