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Potent and Selective Inhibition of Human Cytomegalovirus Replication by 1263W94, a Benzimidazole l-Riboside with a Unique Mode of Action

Antimicrobial Agents and Chemotherapy, 2002-08, Vol.46 (8), p.2365-2372

2002

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Synthesis and Antiviral Activity of Novel Erythrofuranosyl Imidazo[1,2-a]pyridine C-Nucleosides Constructed via Palladium Coupling of Iodoimidazo[1,2-a]pyridines and Dihydrofuran

Journal of medicinal chemistry, 2003-04, Vol.46 (8), p.1449-1455

2003

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Amino Acid Ester Prodrugs of the Antiviral Agent 2-Bromo-5,6-dichloro-1-(β-d-ribofuranosyl)benzimidazole as Potential Substrates of hPEPT1 Transporter

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.1274-1277

2005

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In Vitro Activities of Benzimidazole d- and l-Ribonucleosides against Herpesviruses

Antimicrobial Agents and Chemotherapy, 2003-07, Vol.47 (7), p.2186-2192

2003

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Interaction of the Putative Human Cytomegalovirus Portal Protein pUL104 with the Large Terminase Subunit pUL56 and Its Inhibition by Benzimidazole-d-Ribonucleosides

Journal of Virology, 2005-12, Vol.79 (23), p.14660-14667

2005

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Benzimidazole Analogs Inhibit Human Herpesvirus 6

Antimicrobial Agents and Chemotherapy, 2011-05, Vol.55 (5), p.2442-2445

2011

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Susceptibilities of Human Cytomegalovirus Clinical Isolates and Other Herpesviruses to New Acetylated, Tetrahalogenated Benzimidazole d-Ribonucleosides

Antimicrobial Agents and Chemotherapy, 2009-12, Vol.53 (12), p.5095-5101

2009

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Toyocamycin specifically inhibits auxin signaling mediated by SCFTIR1 pathway

Phytochemistry (Oxford), 2009, Vol.70 (2), p.190-197

2009

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Resistance of Human Cytomegalovirus to the Benzimidazole l-Ribonucleoside Maribavir Maps to UL27

Journal of Virology, 2003-11, Vol.77 (21), p.11499-11506

2003

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Identification of Acetylated, Tetrahalogenated Benzimidazole d-Ribonucleosides with Enhanced Activity against Human Cytomegalovirus

Journal of Virology, 2007-11, Vol.81 (21), p.11604-11611

2007

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Facile Synthesis of 1-Substituted 2-Amino-3-cyanopyrroles: New Synthetic Precursors for 5,6-Unsubstituted Pyrrolo[2,3-d]pyrimidines

Organic letters, 2004-08, Vol.6 (17), p.2857-2859

2004

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Preclinical and Toxicology Studies of 1263W94, a Potent and Selective Inhibitor of Human Cytomegalovirus Replication

Antimicrobial Agents and Chemotherapy, 2002-08, Vol.46 (8), p.2373-2380

2002

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Inhibition of Human Cytomegalovirus Replication by Benzimidazole Nucleosides Involves Three Distinct Mechanisms

Antimicrobial Agents and Chemotherapy, 2004-10, Vol.48 (10), p.3918-3927

2004

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Tetrahalogenated benzimidazole D-ribonucleosides are active against rat cytomegalovirus

Antiviral research, 2017-01, Vol.137, p.102-107

2017

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Inhibition of Human Immunodeficiency Virus Type 1 by Triciribine Involves the Accessory Protein Nef

Antimicrobial Agents and Chemotherapy, 2010-04, Vol.54 (4), p.1512-1519

2010

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Mechanism of Action of the Ribopyranoside Benzimidazole GW275175X against Human Cytomegalovirus

Antimicrobial Agents and Chemotherapy, 2004-05, Vol.48 (5), p.1647-1651

2004

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Role of a Mutation in Human Cytomegalovirus Gene UL104 in Resistance to Benzimidazole Ribonucleosides

Journal of Virology, 2004-01, Vol.78 (2), p.710-715

2004

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Design, Synthesis, and Antiviral Activity of Certain 3-Substituted 2,5,6-Trichloroindole Nucleosides

Journal of medicinal chemistry, 2004-11, Vol.47 (23), p.5753-5765

2004

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Activities of Benzimidazole d- and l-Ribonucleosides in Animal Models of Cytomegalovirus Infections

Antimicrobial Agents and Chemotherapy, 2004-05, Vol.48 (5), p.1749-1755

2004

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Design, Synthesis, and Antiviral Activity of Certain 2,5,6-Trihalo-1-(.beta.-D-ribofuranosyl)benzimidazoles

Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.4098-4105

1995

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Interactions among antiviral drugs acting late in the replication cycle of human cytomegalovirus

Antiviral research, 2002-10, Vol.56 (1), p.61-72

2002

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N-methylpurine DNA glycosylase and 8-oxoguanine dna glycosylase metabolize the antiviral nucleoside 2-bromo-5,6-dichloro-1-(beta-D-ribofuranosyl)benzimidazole

Drug metabolism and disposition, 2006-06, Vol.34 (6), p.1070-1077

2006

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Synthesis and Antiviral Activity of 3-Formyl- and 3-Cyano-2,5,6-trichloroindole Nucleoside Derivatives

Journal of medicinal chemistry, 2004-11, Vol.47 (23), p.5766-5772

2004

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Amino acid ester prodrugs of 2-bromo-5,6-dichloro-1-(beta-D-ribofuranosyl)benzimidazole enhance metabolic stability in vitro and in vivo

The Journal of pharmacology and experimental therapeutics, 2005-08, Vol.314 (2), p.883-890

2005

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Human cytomegalovirus resistance to deoxyribosylindole nucleosides maps to a transversion mutation in the terminase subunit-encoding gene UL89

Antimicrobial agents and chemotherapy, 2015-01, Vol.59 (1), p.226-232

2015

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Potent and Selective Inhibition of Human Cytomegalovirus Replication by 1263W94, a Benzimidazole l-Riboside with a Unique Mode of Action

Synthesis and Antiviral Activity of Novel Erythrofuranosyl Imidazo[1,2-a]pyridine C-Nucleosides Constructed via Palladium Coupling of Iodoimidazo[1,2-a]pyridines and Dihydrofuran

Amino Acid Ester Prodrugs of the Antiviral Agent 2-Bromo-5,6-dichloro-1-(β-d-ribofuranosyl)benzimidazole as Potential Substrates of hPEPT1 Transporter

In Vitro Activities of Benzimidazole d- and l-Ribonucleosides against Herpesviruses

Interaction of the Putative Human Cytomegalovirus Portal Protein pUL104 with the Large Terminase Subunit pUL56 and Its Inhibition by Benzimidazole-d-Ribonucleosides

Benzimidazole Analogs Inhibit Human Herpesvirus 6

Susceptibilities of Human Cytomegalovirus Clinical Isolates and Other Herpesviruses to New Acetylated, Tetrahalogenated Benzimidazole d-Ribonucleosides

Toyocamycin specifically inhibits auxin signaling mediated by SCFTIR1 pathway

Resistance of Human Cytomegalovirus to the Benzimidazole l-Ribonucleoside Maribavir Maps to UL27

Identification of Acetylated, Tetrahalogenated Benzimidazole d-Ribonucleosides with Enhanced Activity against Human Cytomegalovirus

Facile Synthesis of 1-Substituted 2-Amino-3-cyanopyrroles: New Synthetic Precursors for 5,6-Unsubstituted Pyrrolo[2,3-d]pyrimidines

Preclinical and Toxicology Studies of 1263W94, a Potent and Selective Inhibitor of Human Cytomegalovirus Replication

Inhibition of Human Cytomegalovirus Replication by Benzimidazole Nucleosides Involves Three Distinct Mechanisms

Tetrahalogenated benzimidazole D-ribonucleosides are active against rat cytomegalovirus

Inhibition of Human Immunodeficiency Virus Type 1 by Triciribine Involves the Accessory Protein Nef

Mechanism of Action of the Ribopyranoside Benzimidazole GW275175X against Human Cytomegalovirus

Role of a Mutation in Human Cytomegalovirus Gene UL104 in Resistance to Benzimidazole Ribonucleosides

Design, Synthesis, and Antiviral Activity of Certain 3-Substituted 2,5,6-Trichloroindole Nucleosides

Activities of Benzimidazole d- and l-Ribonucleosides in Animal Models of Cytomegalovirus Infections

Design, Synthesis, and Antiviral Activity of Certain 2,5,6-Trihalo-1-(.beta.-D-ribofuranosyl)benzimidazoles

Interactions among antiviral drugs acting late in the replication cycle of human cytomegalovirus

N-methylpurine DNA glycosylase and 8-oxoguanine dna glycosylase metabolize the antiviral nucleoside 2-bromo-5,6-dichloro-1-(beta-D-ribofuranosyl)benzimidazole

Synthesis and Antiviral Activity of 3-Formyl- and 3-Cyano-2,5,6-trichloroindole Nucleoside Derivatives

Amino acid ester prodrugs of 2-bromo-5,6-dichloro-1-(beta-D-ribofuranosyl)benzimidazole enhance metabolic stability in vitro and in vivo

Human cytomegalovirus resistance to deoxyribosylindole nucleosides maps to a transversion mutation in the terminase subunit-encoding gene UL89

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