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Identification of BMS-200475 as a potent and selective inhibitor of hepatitis B virus

Antimicrobial Agents and Chemotherapy, 1997-07, Vol.41 (7), p.1444-1448

1997

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Metabolic Studies on BMS-200475, a New Antiviral Compound Active against Hepatitis B Virus

Antimicrobial Agents and Chemotherapy, 1999-01, Vol.43 (1), p.190-193

1999

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BMS-200475, a novel carbocyclic 2′-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (2), p.127-132

1997

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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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Selective activity and cellular pharmacology of (1R-1 alpha,2 beta,3 alpha)-9-[2,3-bis(hydroxymethyl)cyclobutyl]guanine in herpesvirus-infected cells

Molecular pharmacology, 1991-09, Vol.40 (3), p.446-453

1991

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Synthesis of SQ-33,054, a novel cyclobutane nucleoside with potent antiviral activity

Tetrahedron letters, 1989, Vol.30 (47), p.6453-6456

1989

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Synthesis and antiviral activity of 1-cyclobutyl-5-(2-bromovinyl)uracil nucleoside analogs and related compounds

Journal of medicinal chemistry, 1992-05, Vol.35 (10), p.1799-1806

1992

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Aminodiol HIV Protease Inhibitors. Synthesis And Structure−Activity Relationships Of P1/P1‘ Compounds: Correlation between Lipophilicity and Cytotoxicity

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1991-2007

1996

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Initial Structure-Activity Relationships for a Caprolactam-based Series of Neutral Factor Xa Inhibitors: Lead Identification

Letters in drug design & discovery, 2005-12, Vol.2 (8), p.625-630

2005

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XYLOCANDIN: A NEW COMPLEX OF ANTIFUNGAL PEPTIDES: I. TAXONOMY, ISOLATION AND BIOLOGICAL ACTIVITY

The Journal of Antibiotics, 1987/11/25, Vol.40(11), pp.1515-1519

1987

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Aminodiol HIV protease inhibitors. 1. Design, synthesis, and preliminary SAR

Journal of medicinal chemistry, 1994-06, Vol.37 (12), p.1758-1768

1994

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Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogs

Journal of medicinal chemistry, 1991-04, Vol.34 (4), p.1415-1421

1991

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Aminodiol HIV protease inhibitors. 2. 1,1-Dimethyl-2-hydroxyethyl carbamate derivatives with enhanced potency

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (5), p.459-464

1995

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Solid-phase synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2233-2239

2004

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Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2227-2231

2004

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Synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3229-3233

2002

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Synthesis of potent and highly selective inhibitors of human tryptase

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3235-3238

2002

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XYLOCANDIN: A NEW COMPLEX OF ANTIFUNGAL PEPTIDES: II. STRUCTURAL STUDIES AND CHEMICAL MODIFICATIONS

The Journal of Antibiotics, 1987/11/25, Vol.40(11), pp.1520-1529

1987

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Ketene aminal-based lactam derivatives as a novel class of orally active FXa inhibitors

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (24), p.5453-5458

2005

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Synthesis of potent and selective 2-azepanone inhibitors of human tryptase

Bioorganic & medicinal chemistry letters, 2004-01, Vol.14 (2), p.309-312

2004

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A Practical Asymmetric Synthesis of the Antiviral Agent Lobucavir, BMS-180194

Organic process research & development, 1998-11, Vol.2 (6), p.393-399

1998

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Regioselective Coupling of Tetraalkylammonium Salts of 6-Iodo-2-aminopurine to a Cyclobutyl Triflate: Efficient Preparation of Homochiral BMS-180,194, a Potent Antiviral Carbocyclic Nucleoside

Journal of organic chemistry, 1995-05, Vol.60 (9), p.2902-2905

1995

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AN IMPROVED LARGE SCALE SYNTHESIS OF 2,3-DIHYDROXYTEREPHTHALIC ACID AND DIMETHYL 2,3-DIHYDROXYTEREPHTHLATE

Organic preparations and procedures international, 1999-02, Vol.31 (1), p.106-109

1999

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Aminodiol HIV Protease Inhibitors. Synthesis And Structure−Activity Relationships Of P 1 /P 1 ‘ Compounds: Correlation between Lipophilicity and Cytotoxicity

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1991-2007

1996

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Aminodiol HIV protease inhibitors: Design, synthesis, and preliminary SAR

Journal of medicinal chemistry, 1994-01, Vol.37 (12), p.1758-1768

1994

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Identification of BMS-200475 as a potent and selective inhibitor of hepatitis B virus

Metabolic Studies on BMS-200475, a New Antiviral Compound Active against Hepatitis B Virus

BMS-200475, a novel carbocyclic 2′-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro

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

Selective activity and cellular pharmacology of (1R-1 alpha,2 beta,3 alpha)-9-[2,3-bis(hydroxymethyl)cyclobutyl]guanine in herpesvirus-infected cells

Synthesis of SQ-33,054, a novel cyclobutane nucleoside with potent antiviral activity

Synthesis and antiviral activity of 1-cyclobutyl-5-(2-bromovinyl)uracil nucleoside analogs and related compounds

Aminodiol HIV Protease Inhibitors. Synthesis And Structure−Activity Relationships Of P1/P1‘ Compounds: Correlation between Lipophilicity and Cytotoxicity

Initial Structure-Activity Relationships for a Caprolactam-based Series of Neutral Factor Xa Inhibitors: Lead Identification

XYLOCANDIN: A NEW COMPLEX OF ANTIFUNGAL PEPTIDES: I. TAXONOMY, ISOLATION AND BIOLOGICAL ACTIVITY

Aminodiol HIV protease inhibitors. 1. Design, synthesis, and preliminary SAR

Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogs

Aminodiol HIV protease inhibitors. 2. 1,1-Dimethyl-2-hydroxyethyl carbamate derivatives with enhanced potency

Solid-phase synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors

Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase

Synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors

Synthesis of potent and highly selective inhibitors of human tryptase

XYLOCANDIN: A NEW COMPLEX OF ANTIFUNGAL PEPTIDES: II. STRUCTURAL STUDIES AND CHEMICAL MODIFICATIONS

Ketene aminal-based lactam derivatives as a novel class of orally active FXa inhibitors

Synthesis of potent and selective 2-azepanone inhibitors of human tryptase

A Practical Asymmetric Synthesis of the Antiviral Agent Lobucavir, BMS-180194

Regioselective Coupling of Tetraalkylammonium Salts of 6-Iodo-2-aminopurine to a Cyclobutyl Triflate: Efficient Preparation of Homochiral BMS-180,194, a Potent Antiviral Carbocyclic Nucleoside

AN IMPROVED LARGE SCALE SYNTHESIS OF 2,3-DIHYDROXYTEREPHTHALIC ACID AND DIMETHYL 2,3-DIHYDROXYTEREPHTHLATE

Aminodiol HIV Protease Inhibitors. Synthesis And Structure−Activity Relationships Of P 1 /P 1 ‘ Compounds: Correlation between Lipophilicity and Cytotoxicity

Aminodiol HIV protease inhibitors: Design, synthesis, and preliminary SAR

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