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Inhibition of HIV replication by amino-sugar derivatives

FEBS letters, 1988-09, Vol.237 (1), p.128-132

1988

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Inhibition of alpha-glucosidase I of the glycoprotein-processing enzymes by 6-O-butanoyl castanospermine (MDL 28,574) and its consequences in human immunodeficiency virus-infected T cells

Antimicrobial Agents and Chemotherapy, 1994-08, Vol.38 (8), p.1780-1787

1994

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Isolation and Characterization of the Fungal Metabolite 3-O-Methylviridicatin as an Inhibitor of Tumour Necrosis Factor α-Induced Human Immunodeficiency Virus Replication

Antiviral chemistry & chemotherapy, 1998-03, Vol.9 (2), p.149-155

1998

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Drug Resistance and Drug Combination Features of the Human Immunodeficiency Virus Inhibitor, BCH-10652 [(±)-2′-Deoxy-3′-Oxa-4′-Thiocytidine, dOTC]

Antiviral chemistry & chemotherapy, 2000-07, Vol.11 (4), p.291-301

2000

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Pyrido [1,2a] indole derivatives identified as novel non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1

Antiviral chemistry & chemotherapy, 1999-03, Vol.10 (2), p.79-86

1999

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The ribonucleotide reductase inhibitor ( E)-2′-fluoromethylene-2′-deoxycytidine (MDL 101,731): a potential topical therapy for herpes simplex virus infection

Antiviral Research, 1995-08, Vol.27 (4), p.325-334

1995

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Naturally Occurring Pyrrolizidines: Inhibition of α-Glucosidase 1 and Anti-HIV Activity of One Stereoisomer

Antiviral chemistry & chemotherapy, 1992-10, Vol.3 (5), p.273-277

1992

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MDL 74,968, a new acyclonucleotide analog: activity against human immunodeficiency virus in vitro and in the hu-PBL-SCID.beige mouse model of infection

Antimicrobial Agents and Chemotherapy, 1996-05, Vol.40 (5), p.1072-1077

1996

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The prevention of cell adhesion and the cell-to-cell spread of HIV-1 in vitro by the α-glucosidase 1 inhibitor, 6- O-butanoyl castanospermine (MDL 28574)

Antiviral research, 1994-10, Vol.25 (2), p.169-175

1994

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Stilbene disulfonic acids. CD4 antagonists that block human immunodeficiency virus type-1 growth at multiple stages of the virus life cycle

The Journal of biological chemistry, 1991-07, Vol.266 (20), p.13355-13363

1991

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Potent inhibition of human immunodeficiency virus by MDL 101028, a novel sulphonic acid polymer

Antiviral research, 1995-10, Vol.28 (2), p.159-173

1995

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Detection of human cytomegalovirus in peripheral mononuclear cells and urine samples using PCR

Molecular and cellular probes, 1992-02, Vol.6 (1), p.51-58

1992

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Anti-HIV Activity of MDL 74968, a Novel Acyclonucleotide Derivative of Guanine: Drug Resistance and Drug Combination Effects in Vitro

Antiviral chemistry & chemotherapy, 1996-10, Vol.7 (5), p.253-260

1996

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Synergistic Inhibition of Human Immunodeficiency Virus Type 1 in vitro by 6-0-butanoylcastanospermine (MDL 28574) in Combination with Inhibitors of the Virus-Encoded Reverse Transcriptase and Proteinase

Antiviral chemistry & chemotherapy, 1995-06, Vol.6 (3), p.143-152

1995

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Polyamine biosynthesis in cells infected with different clinical isolates of human cytomegalovirus

Journal of medical virology, 1991-08, Vol.34 (4), p.212-216

1991

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Anti-Human Immunodeficiency Virus Activity, Bioavailability and Drug Resistance Profile of the Novel Proteinase Inhibitor MDL 74,695

Antiviral chemistry & chemotherapy, 1997-06, Vol.8 (3), p.205-214

1997

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Inhibitors of polyamine biosynthesis block human cytomegalovirus replication

Nature (London), 1982-06, Vol.297 (5868), p.690-691

1982

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Basis of Relative Insensitivity of HIV-Infected JM Cells to AZT

Antiviral chemistry & chemotherapy, 1995-10, Vol.6 (5), p.307-311

1995

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Ultrastructural changes and immunocytochemical analysis of human placental trophoblast during short-term culture

Placenta (Eastbourne), 1989-03, Vol.10 (2), p.179-194

1989

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Increased antiviral activity of HIV protease inhibitors of the difluorostatone type bearing (R)-valinol derivatives as novel c-termini

Bioorganic & medicinal chemistry letters, 1994-05, Vol.4 (10), p.1213-1218

1994

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Loss of cytomegalovirus infectivity after treatment with castanospermine or related plant alkaloids correlates with aberrant glycoprotein synthesis

Antiviral research, 1988-11, Vol.10 (1), p.11-26

1988

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Asymptomatic shedding and subsequent transmission of genital herpes simplex virus

Genitourinary Medicine, 1987-04, Vol.63 (2), p.102-105

1987

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The inhibition of human immunodeficiency virus type 1 in vitro by a non-nucleoside reverse transcriptase inhibitor MKC-442, alone and in combination with other anti-HIV compounds

Antiviral research, 1995-03, Vol.26 (2), p.173-187

1995

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The herpes simplex virus type 1 immediate-early protein icp27 is obligately required for the accumulation of a cellular protein during viral infection

Virology (New York, N.Y.), 1989, Vol.168 (1), p.67-72

1989

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Action of Celgosivir (6 O-Butanoyl Castanospermine) against the Pestivirus BVDV: Implications for the Treatment of Hepatitis C

Antiviral chemistry & chemotherapy, 2004-06, Vol.15 (3), p.141-151

2004

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Inhibition of HIV replication by amino-sugar derivatives

Inhibition of alpha-glucosidase I of the glycoprotein-processing enzymes by 6-O-butanoyl castanospermine (MDL 28,574) and its consequences in human immunodeficiency virus-infected T cells

Isolation and Characterization of the Fungal Metabolite 3-O-Methylviridicatin as an Inhibitor of Tumour Necrosis Factor α-Induced Human Immunodeficiency Virus Replication

Drug Resistance and Drug Combination Features of the Human Immunodeficiency Virus Inhibitor, BCH-10652 [(±)-2′-Deoxy-3′-Oxa-4′-Thiocytidine, dOTC]

Pyrido [1,2a] indole derivatives identified as novel non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1

The ribonucleotide reductase inhibitor ( E)-2′-fluoromethylene-2′-deoxycytidine (MDL 101,731): a potential topical therapy for herpes simplex virus infection

Naturally Occurring Pyrrolizidines: Inhibition of α-Glucosidase 1 and Anti-HIV Activity of One Stereoisomer

MDL 74,968, a new acyclonucleotide analog: activity against human immunodeficiency virus in vitro and in the hu-PBL-SCID.beige mouse model of infection

The prevention of cell adhesion and the cell-to-cell spread of HIV-1 in vitro by the α-glucosidase 1 inhibitor, 6- O-butanoyl castanospermine (MDL 28574)

Stilbene disulfonic acids. CD4 antagonists that block human immunodeficiency virus type-1 growth at multiple stages of the virus life cycle

Potent inhibition of human immunodeficiency virus by MDL 101028, a novel sulphonic acid polymer

Detection of human cytomegalovirus in peripheral mononuclear cells and urine samples using PCR

Anti-HIV Activity of MDL 74968, a Novel Acyclonucleotide Derivative of Guanine: Drug Resistance and Drug Combination Effects in Vitro

Synergistic Inhibition of Human Immunodeficiency Virus Type 1 in vitro by 6-0-butanoylcastanospermine (MDL 28574) in Combination with Inhibitors of the Virus-Encoded Reverse Transcriptase and Proteinase

Polyamine biosynthesis in cells infected with different clinical isolates of human cytomegalovirus

Anti-Human Immunodeficiency Virus Activity, Bioavailability and Drug Resistance Profile of the Novel Proteinase Inhibitor MDL 74,695

Inhibitors of polyamine biosynthesis block human cytomegalovirus replication

Basis of Relative Insensitivity of HIV-Infected JM Cells to AZT

Ultrastructural changes and immunocytochemical analysis of human placental trophoblast during short-term culture

Increased antiviral activity of HIV protease inhibitors of the difluorostatone type bearing (R)-valinol derivatives as novel c-termini

Loss of cytomegalovirus infectivity after treatment with castanospermine or related plant alkaloids correlates with aberrant glycoprotein synthesis

Asymptomatic shedding and subsequent transmission of genital herpes simplex virus

The inhibition of human immunodeficiency virus type 1 in vitro by a non-nucleoside reverse transcriptase inhibitor MKC-442, alone and in combination with other anti-HIV compounds

The herpes simplex virus type 1 immediate-early protein icp27 is obligately required for the accumulation of a cellular protein during viral infection

Action of Celgosivir (6 O-Butanoyl Castanospermine) against the Pestivirus BVDV: Implications for the Treatment of Hepatitis C

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