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Effects of channel modulators on cloned large-conductance calcium-activated potassium channels

Molecular pharmacology, 1996-07, Vol.50 (1), p.206

1996

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787 BMS-766, A NOVEL HCV NS5A INHIBITOR WITH ENHANCED RESISTANCE COVERAGE

Journal of hepatology, 2011-03, Vol.54, p.S316-S316

2011

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The substituted benzimidazolone NS004 is an opener of the cystic fibrosis chloride channel

The Journal of biological chemistry, 1994-04, Vol.269 (15), p.10983-10986

1994

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Molecular mechanism underlying the action of a novel fusion inhibitor of influenza A virus

Journal of Virology, 1997-05, Vol.71 (5), p.4062-4070

1997

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HIV-1 entry – an expanding portal for drug discovery

Drug Discovery Today, 2000-05, Vol.5 (5), p.183-194

2000

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Drug discoverers - you need us! - Reply

Drug discovery today, 2001-07, Vol.6 (13), p.664-665

Meanwell, N A.

2001

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A Small Molecule HIV-1 Inhibitor That Targets the HIV-1 Envelope and Inhibits CD4 Receptor Binding

Proceedings of the National Academy of Sciences - PNAS, 2003-09, Vol.100 (19), p.11013-11018

2003

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1,2-Benzisothiazol-3-one 1,1-Dioxide Inhibitors of Human Mast Cell Tryptase

Journal of medicinal chemistry, 1998-11, Vol.41 (24), p.4854-4860

1998

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Opening of large-conductance calcium-activated potassium channels by the substituted benzimidazolone NS004

Journal of neurophysiology, 1994-05, Vol.71 (5), p.1873-1882

1994

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Azetidin-2-one derivatives as inhibitors of thrombin

Bioorganic & medicinal chemistry, 1995-08, Vol.3 (8), p.1123-1143

1995

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Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor

Journal of antimicrobial chemotherapy, 2005-03, Vol.55 (3), p.289-292

2005

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Salicylamide inhibitors of influenza virus fusion

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1649-1652

2000

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Regioselective Monobenzoylation of Unsymmetrical Piperazines

Journal of organic chemistry, 2000-07, Vol.65 (15), p.4740-4742

2000

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Discovery of a novel class of BK channel openers : Enantiospecific synthesis and BK channel opening activity of 3-(5-chloro-2-hydroxyphenyl)-1,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2-one

Bioorganic & medicinal chemistry letters, 1997-05, Vol.7 (10), p.1255-1260

1997

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A general method for the synthesis of isatins: Preparation of regiospecifically functionalized isatins from anilines

Tetrahedron letters, 1994-10, Vol.35 (40), p.7303-7306

1994

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Orally Active Fusion Inhibitor of Respiratory Syncytial Virus

Antimicrobial Agents and Chemotherapy, 2004-02, Vol.48 (2), p.413-422

2004

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An approach to the identification of potent inhibitors of influenza virus fusion using parallel synthesis methodology

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (17), p.2393-2396

2001

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Solid-phase synthesis of benzisothiazolones as serine protease inhibitors

Bioorganic & medicinal chemistry letters, 1999-03, Vol.9 (5), p.663-666

1999

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pH-Dependent Changes in Photoaffinity Labeling Patterns of the H1 Influenza Virus Hemagglutinin by Using an Inhibitor of Viral Fusion

Journal of Virology, 1999-03, Vol.73 (3), p.1785-1794

1999

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Oral Efficacy of a Respiratory Syncytial Virus Inhibitor in Rodent Models of Infection

Antimicrobial Agents and Chemotherapy, 2004-07, Vol.48 (7), p.2448-2454

2004

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Novel quinolizidine salicylamide influenza fusion inhibitors

Bioorganic & medicinal chemistry letters, 1999-08, Vol.9 (15), p.2177-2180

1999

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Taking aim at a moving target — inhibitors of influenza virus Part 2: viral replication, packaging and release

Drug discovery today, 1996, Vol.1 (9), p.388-397

1996

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Identification of N-Hydroxamic Acid and N-Hydroxyimide Compounds that Inhibit the Influenza Virus Polymerase

Antiviral chemistry & chemotherapy, 1996-12, Vol.7 (6), p.353-360

1996

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Nonprostanoid prostacyclin mimetics. 5. Structure-activity relationships associated with [3-[4-(4,5-diphenyl-2-oxazolyl)-5-oxazolyl]phenoxy]acetic acid

Journal of medicinal chemistry, 1993-11, Vol.36 (24), p.3884-3903

1993

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Novel 3 ′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide

Tetrahedron letters, 2004-01, Vol.45 (4), p.739-742

2004

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Effects of channel modulators on cloned large-conductance calcium-activated potassium channels

787 BMS-766, A NOVEL HCV NS5A INHIBITOR WITH ENHANCED RESISTANCE COVERAGE

The substituted benzimidazolone NS004 is an opener of the cystic fibrosis chloride channel

Molecular mechanism underlying the action of a novel fusion inhibitor of influenza A virus

HIV-1 entry – an expanding portal for drug discovery

Drug discoverers - you need us! - Reply

A Small Molecule HIV-1 Inhibitor That Targets the HIV-1 Envelope and Inhibits CD4 Receptor Binding

1,2-Benzisothiazol-3-one 1,1-Dioxide Inhibitors of Human Mast Cell Tryptase

Opening of large-conductance calcium-activated potassium channels by the substituted benzimidazolone NS004

Azetidin-2-one derivatives as inhibitors of thrombin

Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor

Salicylamide inhibitors of influenza virus fusion

Regioselective Monobenzoylation of Unsymmetrical Piperazines

Discovery of a novel class of BK channel openers : Enantiospecific synthesis and BK channel opening activity of 3-(5-chloro-2-hydroxyphenyl)-1,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2-one

A general method for the synthesis of isatins: Preparation of regiospecifically functionalized isatins from anilines

Orally Active Fusion Inhibitor of Respiratory Syncytial Virus

An approach to the identification of potent inhibitors of influenza virus fusion using parallel synthesis methodology

Solid-phase synthesis of benzisothiazolones as serine protease inhibitors

pH-Dependent Changes in Photoaffinity Labeling Patterns of the H1 Influenza Virus Hemagglutinin by Using an Inhibitor of Viral Fusion

Oral Efficacy of a Respiratory Syncytial Virus Inhibitor in Rodent Models of Infection

Novel quinolizidine salicylamide influenza fusion inhibitors

Taking aim at a moving target — inhibitors of influenza virus Part 2: viral replication, packaging and release

Identification of N-Hydroxamic Acid and N-Hydroxyimide Compounds that Inhibit the Influenza Virus Polymerase

Nonprostanoid prostacyclin mimetics. 5. Structure-activity relationships associated with [3-[4-(4,5-diphenyl-2-oxazolyl)-5-oxazolyl]phenoxy]acetic acid

Novel 3 ′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide

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