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Urea−PETT Compounds as a New Class of HIV-1 Reverse Transcriptase Inhibitors. 3. Synthesis and Further Structure−Activity Relationship Studies of PETT Analogues

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4150-4160

1999

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Retention of prefabricated and individually cast root canal posts in vitro

British dental journal, 2003-08, Vol.195 (3), p.155-158

2003

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A retrospective study of pre-fabricated carbon fibre root canal posts

Journal of oral rehabilitation, 2003-10, Vol.30 (10), p.1036-1040

2003

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Prevention of simian immunodeficiency virus, SIVsm, or HIV-2 infection in cynomolgus monkeys by pre- and postexposure administration of BEA-005

AIDS (London), 1997-02, Vol.11 (2), p.157-162

1997

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Structure-activity relationships for phosphorylation of nucleoside analogs to monophosphates by nucleoside kinases

Acta biochimica polonica, 1996-01, Vol.43 (1), p.143-160

1996

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The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase

Antimicrobial Agents and Chemotherapy, 1995-06, Vol.39 (6), p.1329-1335

1995

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Phenethylthiazolethiourea (PETT) Compounds, a New Class of HIV-1 Reverse Transcriptase Inhibitors. 1. Synthesis and Basic Structure-Activity Relationship Studies of PETT Analogs

Journal of medicinal chemistry, 1995-12, Vol.38 (25), p.4929-4936

1995

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Comparison of the substrate specificities of human thymidine kinase 1 and 2 and deoxycytidine kinase toward antiviral and cytostatic nucleoside analogs

Biochemical and biophysical research communications, 1991-04, Vol.176 (2), p.586-592

1991

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Distribution to the Brain and Protein Binding of 3′and 5-Substituted 2′,3′-Dideoxyuridine Derivatives, Studied by Microdialysis

Antiviral chemistry & chemotherapy, 1997-01, Vol.8 (1), p.47-53

1997

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Acyclonucleoside analogue inhibitors of mammalian purine nucleoside phosphorylase

Biochemical pharmacology, 1991-06, Vol.41 (12), p.1791-1803

1991

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Mode of action, toxicity, pharmacokinetics, and efficacy of some new antiherpesvirus guanosine analogs related to buciclovir

Antimicrobial Agents and Chemotherapy, 1986-10, Vol.30 (4), p.598-605

1986

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Phenethylthiazolylthiourea (PETT) Compounds as a New Class of HIV-1 Reverse Transcriptase Inhibitors. 2. Synthesis and Further Structure−Activity Relationship Studies of PETT Analogs

Journal of medicinal chemistry, 1996-10, Vol.39 (21), p.4261-4274

1996

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Antiherpetic activity and mechanism of action of 9-(4-hydroxybutyl)guanine

Antiviral research, 1983-08, Vol.3 (2), p.77-86

1983

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Antiherpes effects and pharmacokinetic properties of 9-(4-hydroxybutyl) guanine and the (R) and (S) enantiomers of 9-(3,4-dihydroxybutyl)guanine

Antimicrobial Agents and Chemotherapy, 1985-05, Vol.27 (5), p.753-759

1985

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9-(3,4-dihydroxybutyl)guanine, a new inhibitor of herpesvirus multiplication

Antimicrobial Agents and Chemotherapy, 1983-05, Vol.23 (5), p.664-670

1983

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Synthesis of Various 5-(5″-Substituted-3″-Bromophenyl)-2′-β-Deoxyuridines

Antiviral chemistry & chemotherapy, 1996-04, Vol.7 (2), p.94-100

1996

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Thienyl-Substituted Nucleosides and Their Triphosphates

Antiviral chemistry & chemotherapy, 1994-12, Vol.5 (6), p.395-402

1994

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An analysis of the inhibition of replication of HIV and MULV by some 3'-blocked pyrimidine analogs

Biochemical pharmacology, 1989, Vol.38 (1), p.109-119

1989

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The relative merits and drawbacks of new nucleoside analogues with clinical potential

Journal of antimicrobial chemotherapy, 1984-01, Vol.14 (suppl-A), p.5-26

1984

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Light-Activated Liposomes Coated with Hyaluronic Acid as a Potential Drug Delivery System

Pharmaceutics, 2020-08, Vol.12 (8), p.763

2020

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Trisodium Phosphonoformate, a New Antiviral Compound

Science (American Association for the Advancement of Science), 1978-09, Vol.201 (4358), p.819-821

1978

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Synthesis of Mimics to 5-(2″-thienyl)-2′,3′-β-Dideoxyuridine Triphosphate

Antiviral chemistry & chemotherapy, 1996-04, Vol.7 (2), p.101-107

1996

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Synthesis of 2′- and 3′-Amino-Substituted Uridine, Thymidine and Adenosine, and Their Inhibitions of HIV Replication

Antiviral chemistry & chemotherapy, 1990-06, Vol.1 (3), p.183-202

1990

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Inhibition of SIV and HIV-2 Replication in Cynomolgus Monkeys by (-)9-[4-Hydroxy-2-(Hydroxymethyl)-Butyl]Guanine (H2G)

Antiviral chemistry & chemotherapy, 1996-01, Vol.7 (1), p.21-26

1996

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Inhibition of Influenza Virus Ribonucleic Acid Polymerase by Ribavirin Triphosphate

Antimicrobial Agents and Chemotherapy, 1977-06, Vol.11 (6), p.946-951

1977

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Urea−PETT Compounds as a New Class of HIV-1 Reverse Transcriptase Inhibitors. 3. Synthesis and Further Structure−Activity Relationship Studies of PETT Analogues

Retention of prefabricated and individually cast root canal posts in vitro

A retrospective study of pre-fabricated carbon fibre root canal posts

Prevention of simian immunodeficiency virus, SIVsm, or HIV-2 infection in cynomolgus monkeys by pre- and postexposure administration of BEA-005

Structure-activity relationships for phosphorylation of nucleoside analogs to monophosphates by nucleoside kinases

The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase

Phenethylthiazolethiourea (PETT) Compounds, a New Class of HIV-1 Reverse Transcriptase Inhibitors. 1. Synthesis and Basic Structure-Activity Relationship Studies of PETT Analogs

Comparison of the substrate specificities of human thymidine kinase 1 and 2 and deoxycytidine kinase toward antiviral and cytostatic nucleoside analogs

Distribution to the Brain and Protein Binding of 3′and 5-Substituted 2′,3′-Dideoxyuridine Derivatives, Studied by Microdialysis

Acyclonucleoside analogue inhibitors of mammalian purine nucleoside phosphorylase

Mode of action, toxicity, pharmacokinetics, and efficacy of some new antiherpesvirus guanosine analogs related to buciclovir

Phenethylthiazolylthiourea (PETT) Compounds as a New Class of HIV-1 Reverse Transcriptase Inhibitors. 2. Synthesis and Further Structure−Activity Relationship Studies of PETT Analogs

Antiherpetic activity and mechanism of action of 9-(4-hydroxybutyl)guanine

Antiherpes effects and pharmacokinetic properties of 9-(4-hydroxybutyl) guanine and the (R) and (S) enantiomers of 9-(3,4-dihydroxybutyl)guanine

9-(3,4-dihydroxybutyl)guanine, a new inhibitor of herpesvirus multiplication

Synthesis of Various 5-(5″-Substituted-3″-Bromophenyl)-2′-β-Deoxyuridines

Thienyl-Substituted Nucleosides and Their Triphosphates

An analysis of the inhibition of replication of HIV and MULV by some 3'-blocked pyrimidine analogs

The relative merits and drawbacks of new nucleoside analogues with clinical potential

Light-Activated Liposomes Coated with Hyaluronic Acid as a Potential Drug Delivery System

Trisodium Phosphonoformate, a New Antiviral Compound

Synthesis of Mimics to 5-(2″-thienyl)-2′,3′-β-Dideoxyuridine Triphosphate

Synthesis of 2′- and 3′-Amino-Substituted Uridine, Thymidine and Adenosine, and Their Inhibitions of HIV Replication

Inhibition of SIV and HIV-2 Replication in Cynomolgus Monkeys by (-)9-[4-Hydroxy-2-(Hydroxymethyl)-Butyl]Guanine (H2G)

Inhibition of Influenza Virus Ribonucleic Acid Polymerase by Ribavirin Triphosphate

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