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Schols D

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Publications:

Title Authors Year Journal
A Multi-targeted Drug Candidate with Dual Anti-HIV and Anti-HSV Activity. Schols D 2013 PLoS pathogens
New Nitrogen Containing Substituents at the Indole-2-carboxamide Yield High Potent and Broad Spectrum Indolylarylsulfone HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors. Schols D 2012 Journal of medicinal chemistry
Indolylarylsulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: new cyclic substituents at indole-2-carboxamide. Schols D 2011 Journal of medicinal chemistry
Therapeutic strategies towards HIV-1 infection in macrophages. Schols D 2006 Antiviral research
Marked depletion of glycosylation sites in HIV-1 gp120 under selection pressure by the mannose-specific plant lectins of Hippeastrum hybrid and Galanthus nivalis. Schols D 2005 Molecular pharmacology
Pyridine N-oxide derivatives: unusual anti-HIV compounds with multiple mechanisms of antiviral action. Schols D 2005 The Journal of antimicrobial chemotherapy
CADA, a novel CD4-targeted HIV inhibitor, is synergistic with various anti-HIV drugs in vitro. Schols D 2004 AIDS (London, England)
Development of a cell-based enzyme-linked immunosorbent assay for high-throughput screening of HIV type 1 entry inhibitors targeting the coreceptor CXCR4. Schols D 2003 AIDS research and human retroviruses
2-Chloro-3-pyridin-3-yl-5,6,7,8-tetrahydroindolizine-1-carboxamide (CMV423), a new lead compound for the treatment of human cytomegalovirus infections. Schols D 2002 Antiviral research
Inhibition of HIV infection by CXCR4 and CCR5 chemokine receptor antagonists. Schols D 2001 Antiviral chemistry & chemotherapy
Polyanionic (i.e., polysulfonate) dendrimers can inhibit the replication of human immunodeficiency virus by interfering with both virus adsorption and later steps (reverse transcriptase/integrase) in the virus replicative cycle. Schols D 2000 Molecular pharmacology
9-(2-Phosphonylmethoxyethyl)adenine induces tumor cell differentiation or cell death by blocking cell cycle progression through the S phase. Schols D 1999 Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research
SRR-SB3, a disulfide-containing macrolide that inhibits a late stage of the replicative cycle of human immunodeficiency virus. Schols D 1997 Antimicrobial agents and chemotherapy
Highly favorable antiviral activity and resistance profile of the novel thiocarboxanilide pentenyloxy ether derivatives UC-781 and UC-82 as inhibitors of human immunodeficiency virus type 1 replication. Schols D 1996 Molecular pharmacology
New tetrahydroimidazo[4,5,1-jk][1,4]-benzodiazepin-2(1H)-one and -thione derivatives are potent inhibitors of human immunodeficiency virus type 1 replication and are synergistic with 2',3'-dideoxynucleoside analogs. Schols D 1994 Antimicrobial agents and chemotherapy
Mechanism of anti-human immunodeficiency virus action of polyoxometalates, a class of broad-spectrum antiviral agents. Schols D 1992 Molecular pharmacology
2',5'-Bis-O-(tert-butyldimethylsilyl)-3'-spiro-5''-(4''-amino-1'',2''- oxathiole-2'',2'-dioxide)pyrimidine (TSAO) nucleoside analogues: highlyselective inhibitors of human immunodeficiency virus type 1 that are targeted at the viral reverse transcriptase. Schols D 1992 Proceedings of the National Academy of Sciences of the United States of America
Anti-human immunodeficiency virus effects of cationic metalloporphyrin-ellipticine complexes. Schols D 1992 Biochemical pharmacology
Synthesis and anti-HIV activities of low molecular weight aurintricarboxylic acid fragments and related compounds. Schols D 1991 Journal of medicinal chemistry
Preparation and anti-HIV activities of aurintricarboxylic acid fractions and analogues: direct correlation of antiviral potency with molecular weight. Schols D 1991 Journal of medicinal chemistry
Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative. Schols D 1989 Biochemical and biophysical research communications
Selective activity of several cholic acid derivatives against human immunodeficiency virus replication in vitro. Schols D 1989 Journal of acquired immune deficiency syndromes
Flow cytometric method to demonstrate whether anti-HIV-1 agents inhibit virion binding to T4+ cells. Schols D 1989 Journal of acquired immune deficiency syndromes
Fuchsin acid selectively inhibits human immunodeficiency virus (HIV) replication in vitro. Schols D 1988 Biochemical and biophysical research communications

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