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A combined in silico/in vitro approach unveils common molecular requirements for efficient BVDV RdRp binding of linear aromatic N-polycyclic systems

European journal of medicinal chemistry, 2016-07, Vol.117, p.321-334

2016

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Synthesis and Antiviral Evaluation of 1-[(2-Phenoxyethyl)oxymethyl] and 6-(3,5-Dimethoxybenzyl) Analogues of HIV Drugs Emivirine and TNK-651

Drug research, 2016-04, Vol.66 (4), p.181

2016

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Structure-Based Design, Synthesis, and Biological Evaluation of Conformationally Restricted Novel 2-Alkylthio-6-[1-(2,6-difluorophenyl)alkyl]- 3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase

Journal of medicinal chemistry, 2001-08, Vol.44 (16), p.2544-2554

2001

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Synthesis and anti-picornaviridae in vitro activity of a new class of helicase inhibitors the N,N'-bis[4-(1H(2H)-benzotriazol-1(2)-yl)phenyl] alkyldicarboxamides

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2007-11, Vol.3 (6), p.520

2007

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2-Arylbenzimidazoles as antiviral and antiproliferative agents. Part 1

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2008-11, Vol.4 (6), p.605

2008

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Preliminary Anti-Coxsackie Activity of Novel 1-[4-(5,6-dimethyl(H)- 1H(2H)-benzotriazol-1(2)-yl)phenyl]-3-alkyl(aryl)ureas

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2020-01, Vol.16 (5), p.677

2020

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Antiviral activity of indole derivatives

Antiviral research, 2009-08, Vol.83 (2), p.179-185

2009

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Simple, Short Peptide Derivatives of a Sulfonylindolecarboxamide (L-737,126) Active in Vitro against HIV-1 Wild Type and Variants Carrying Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations

Journal of medicinal chemistry, 2004-10

2004

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Synthesis, antimicrobial activity and molecular modeling studies of halogenated 4-[1H-imidazol-1-yl(phenyl)methyl]- 1,5-diphenyl-1H-pyrazoles

Bioorganic & medicinal chemistry, 2004-10, Vol.12 (20), p.5465-5483

2004

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Topical nonnucleoside reverse transcriptase inhibitor MC 1220 partially prevents vaginal RT-SHIV infection of macaques

AIDS research and human retroviruses, 2011-09, Vol.27 (9), p.933

2011

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Antitumor Agents. 3. Design, Synthesis, and Biological Evaluation of New Pyridoisoquinolindione and Dihydrothienoquinolindione Derivatives with Potent Cytotoxic Activity

Journal of medicinal chemistry, 2004-02, Vol.47 (4), p.849-858

2004

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Simple, Short Peptide Derivatives of a Sulfonylindolecarboxamide (L-737,126) Active in Vitro against HIV-1 Wild Type and Variants Carrying Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations

Journal of medicinal chemistry, 2004-07, Vol.47 (15), p.3892-3896

2004

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2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone: novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays

Bioorganic & medicinal chemistry, 2004-01, Vol.12 (1), p.199-215

2004

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Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5′-α-hydroxyphosphonates

Bioorganic & medicinal chemistry, 2006-03, Vol.14 (6), p.1924-1934

2006

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Synthesis and in vitro antimycobacterial activity of novel 3-(1 H-pyrrol-1-yl)-2-oxazolidinone analogues of PNU-100480

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (6), p.1537-1541

2004

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Structure—Activity Relationship Studies on New DABOs: Effect of Substitutions at Pyrimidine C-5 and C-6 Positions on Anti-HIV-1 Activity

Antiviral chemistry & chemotherapy, 2001-01, Vol.12 (1), p.37-50

2001

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Structure-Based Design, Parallel Synthesis, Structure−Activity Relationship, and Molecular Modeling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea Derivatives

Journal of medicinal chemistry, 2005-06, Vol.48 (11), p.3858-3873

2005

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Antitumor Agents. 2. Synthesis, Structure−Activity Relationships, and Biological Evaluation of Substituted 5H-Pyridophenoxazin-5-ones with Potent Antiproliferative Activity

Journal of medicinal chemistry, 2002-11, Vol.45 (24), p.5217-5223

2002

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Synthesis, Biological Evaluation, and Binding Mode of Novel 1-[2-(Diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles Targeted at the HIV-1 Reverse Transcriptase

Journal of medicinal chemistry, 2002-04, Vol.45 (8), p.1567-1576

2002

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Extraction of Juniperus communis L. ssp. nana Willd. essential oil by supercritical carbon dioxide

Flavour and fragrance journal, 2006-01, Vol.21 (1), p.148-154

2006

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Antitumor Agents. 1. Synthesis, Biological Evaluation, and Molecular Modeling of 5H-Pyrido[3,2-a]phenoxazin-5-one, a Compound with Potent Antiproliferative Activity

Journal of medicinal chemistry, 2002-11, Vol.45 (24), p.5205-5216

2002

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In-water reactivity of nucleosides and nucleotides: one-step preparation and biological evaluation of novel ferrocenyl-derivatives

Tetrahedron, 2004-07, Vol.60 (31), p.6555-6563

2004

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6-Aryl-2,4-dioxo-5-hexenoic acids, novel integrase inhibitors active against HIV-1 multiplication in cell-based assays

Bioorganic & medicinal chemistry letters, 2004-04, Vol.14 (7), p.1745-1749

2004

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Synthesis and antiproliferative activity of 3-aryl-2-(1 H-benzotriazol-1-yl)acrylonitriles. Part III

European journal of medicinal chemistry, 2002-11, Vol.37 (11), p.891-900

2002

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Synthesis, in vitro Antiproliferative and Anti-HIV Activity of New Derivatives of 2-Piperazino-1,3-benzo[d]thiazoles

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 2010-11, Vol.65 (11), p.1372-1380

2010

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A combined in silico/in vitro approach unveils common molecular requirements for efficient BVDV RdRp binding of linear aromatic N-polycyclic systems

Synthesis and Antiviral Evaluation of 1-[(2-Phenoxyethyl)oxymethyl] and 6-(3,5-Dimethoxybenzyl) Analogues of HIV Drugs Emivirine and TNK-651

Structure-Based Design, Synthesis, and Biological Evaluation of Conformationally Restricted Novel 2-Alkylthio-6-[1-(2,6-difluorophenyl)alkyl]- 3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase

Synthesis and anti-picornaviridae in vitro activity of a new class of helicase inhibitors the N,N'-bis[4-(1H(2H)-benzotriazol-1(2)-yl)phenyl] alkyldicarboxamides

2-Arylbenzimidazoles as antiviral and antiproliferative agents. Part 1

Preliminary Anti-Coxsackie Activity of Novel 1-[4-(5,6-dimethyl(H)- 1H(2H)-benzotriazol-1(2)-yl)phenyl]-3-alkyl(aryl)ureas

Antiviral activity of indole derivatives

Simple, Short Peptide Derivatives of a Sulfonylindolecarboxamide (L-737,126) Active in Vitro against HIV-1 Wild Type and Variants Carrying Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations

Synthesis, antimicrobial activity and molecular modeling studies of halogenated 4-[1H-imidazol-1-yl(phenyl)methyl]- 1,5-diphenyl-1H-pyrazoles

Topical nonnucleoside reverse transcriptase inhibitor MC 1220 partially prevents vaginal RT-SHIV infection of macaques

Antitumor Agents. 3. Design, Synthesis, and Biological Evaluation of New Pyridoisoquinolindione and Dihydrothienoquinolindione Derivatives with Potent Cytotoxic Activity

Simple, Short Peptide Derivatives of a Sulfonylindolecarboxamide (L-737,126) Active in Vitro against HIV-1 Wild Type and Variants Carrying Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations

2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone: novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays

Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5′-α-hydroxyphosphonates

Synthesis and in vitro antimycobacterial activity of novel 3-(1 H-pyrrol-1-yl)-2-oxazolidinone analogues of PNU-100480

Structure—Activity Relationship Studies on New DABOs: Effect of Substitutions at Pyrimidine C-5 and C-6 Positions on Anti-HIV-1 Activity

Structure-Based Design, Parallel Synthesis, Structure−Activity Relationship, and Molecular Modeling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea Derivatives

Antitumor Agents. 2. Synthesis, Structure−Activity Relationships, and Biological Evaluation of Substituted 5H-Pyridophenoxazin-5-ones with Potent Antiproliferative Activity

Synthesis, Biological Evaluation, and Binding Mode of Novel 1-[2-(Diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles Targeted at the HIV-1 Reverse Transcriptase

Extraction of Juniperus communis L. ssp. nana Willd. essential oil by supercritical carbon dioxide

Antitumor Agents. 1. Synthesis, Biological Evaluation, and Molecular Modeling of 5H-Pyrido[3,2-a]phenoxazin-5-one, a Compound with Potent Antiproliferative Activity

In-water reactivity of nucleosides and nucleotides: one-step preparation and biological evaluation of novel ferrocenyl-derivatives

6-Aryl-2,4-dioxo-5-hexenoic acids, novel integrase inhibitors active against HIV-1 multiplication in cell-based assays

Synthesis and antiproliferative activity of 3-aryl-2-(1 H-benzotriazol-1-yl)acrylonitriles. Part III

Synthesis, in vitro Antiproliferative and Anti-HIV Activity of New Derivatives of 2-Piperazino-1,3-benzo[d]thiazoles

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