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Multipurpose Prevention Technologies: Opportunities and Challenges to Ensure Advancement of the Most Promising MPTs

Frontiers in reproductive health, 2021-09, Vol.3, p.704841-704841

2021

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Isolation and Characterization of Griffithsin, a Novel HIV-inactivating Protein, from the Red Alga Griffithsia sp.

The Journal of biological chemistry, 2005-03, Vol.280 (10), p.9345-9353

2005

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Editorial: Multipurpose prevention technologies: call for innovative strategies to address critical priorities and gaps

Frontiers in reproductive health, 2024-05, Vol.6, p.1417974-1417974

2024

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Shikonin, a Component of Chinese Herbal Medicine, Inhibits Chemokine Receptor Function and Suppresses Human Immunodeficiency Virus Type 1

Antimicrobial Agents and Chemotherapy, 2003-09, Vol.47 (9), p.2810-2816

2003

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Potent Anti-Influenza Activity of Cyanovirin-N and Interactions with Viral Hemagglutinin

Antimicrobial Agents and Chemotherapy, 2003-08, Vol.47 (8), p.2518-2525

2003

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In Vitro Preclinical Testing of Nonoxynol-9 as Potential Anti-Human Immunodeficiency Virus Microbicide: a Retrospective Analysis of Results from Five Laboratories

Antimicrobial Agents and Chemotherapy, 2006-02, Vol.50 (2), p.713-723

2006

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FDA Public Meeting Report on “Drug Interactions With Hormonal Contraceptives: Public Health and Drug Development Implications”

Journal of clinical pharmacology, 2018-12, Vol.58 (12), p.1655-1665

2018

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A Summary of the Sixth International Workshop on Microbiome in HIV Pathogenesis, Prevention, and Treatment

AIDS research and human retroviruses, 2022-03, Vol.38 (3), p.173

2022

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Considerations and development of topical microbicides to inhibit the sexual transmission of HIV

Expert opinion on investigational drugs, 2002-08, Vol.11 (8), p.1077-1097

Turpin, Jim A

2002

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Functional homologs of cyanovirin-N amenable to mass production in prokaryotic and eukaryotic hosts

Protein expression and purification, 2002-10, Vol.26 (1), p.42-49

2002

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The next generation of HIV/AIDS drugs: novel and developmental antiHIV drugs and targets

Expert review of anti-infective therapy, 2003-06, Vol.1 (1), p.97-128

Turpin, Jim A

2003

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The Biological Effects of Structural Variation at the Meta Position of the Aromatic Rings and at the End of the Alkenyl Chain in the Alkenyldiarylmethane Series of Non-Nucleoside Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 2001-11, Vol.44 (24), p.4092-4113

2001

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Outcomes of a National Institute of Allergy and Infectious Diseases Workshop on understanding HIV-exposed but seronegative individuals

AIDS research and human retroviruses, 2011-07, Vol.27 (7), p.737

2011

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Solid-Phase Synthesis of the Alkenyldiarylmethane (ADAM) Series of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

Journal of organic chemistry, 2001-09, Vol.66 (18), p.5958-5964

2001

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Synthesis and anti-HIV activity of a bile acid analog of cosalane

Tetrahedron, 2001-11, Vol.57 (46), p.9385-9391

2001

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Inhibition of Acute-, Latent-, and Chronic-Phase Human Immunodeficiency Virus Type 1 (HIV-1) Replication by a Bistriazoloacridone Analog That Selectively Inhibits HIV-1 Transcription

Antimicrobial Agents and Chemotherapy, 1998-03, Vol.42 (3), p.487-494

1998

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Chicoric Acid Analogues as HIV-1 Integrase Inhibitors

Journal of medicinal chemistry, 1999-04, Vol.42 (8), p.1401-1414

1999

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Benzamide-Based Thiolcarbamates: A New Class of HIV-1 NCp7 Inhibitors

Bioorganic & medicinal chemistry letters, 2002-03, Vol.12 (5), p.767-770

2002

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Antiviral activity of hop constituents against a series of DNA and RNA viruses

Antiviral research, 2004, Vol.61 (1), p.57-62

2004

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Anti-HIV Agents That Selectively Target Retroviral Nucleocapsid Protein Zinc Fingers without Affecting Cellular Zinc Finger Proteins

Journal of medicinal chemistry, 1998-04, Vol.41 (9), p.1371-1381

1998

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Metal-Dependent Inhibition of HIV-1 Integrase

Journal of medicinal chemistry, 2002-12, Vol.45 (26), p.5661-5670

2002

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Synthesis and Biological Properties of Novel Pyridinioalkanoyl Thiolesters (PATE) as Anti-HIV-1 Agents That Target the Viral Nucleocapsid Protein Zinc Fingers

Journal of medicinal chemistry, 1999-01, Vol.42 (1), p.67-86

1999

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Optimization of unique, uncharged thioesters as inhibitors of HIV replication

Bioorganic & medicinal chemistry, 2004-12, Vol.12 (24), p.6437-6450

2004

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The Secondary Amine/Nitric Oxide Complex Ion R2N[N(O)NO]- as Nucleophile and Leaving Group in SNAr Reactions

Journal of organic chemistry, 2001-05, Vol.66 (9), p.3090-3098

2001

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SJ-3366, a Unique and Highly Potent Nonnucleoside Reverse Transcriptase Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1) That Also Inhibits HIV-2

Antimicrobial Agents and Chemotherapy, 2001-02, Vol.45 (2), p.393-400

2001

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Multipurpose Prevention Technologies: Opportunities and Challenges to Ensure Advancement of the Most Promising MPTs

Isolation and Characterization of Griffithsin, a Novel HIV-inactivating Protein, from the Red Alga Griffithsia sp.

Editorial: Multipurpose prevention technologies: call for innovative strategies to address critical priorities and gaps

Shikonin, a Component of Chinese Herbal Medicine, Inhibits Chemokine Receptor Function and Suppresses Human Immunodeficiency Virus Type 1

Potent Anti-Influenza Activity of Cyanovirin-N and Interactions with Viral Hemagglutinin

In Vitro Preclinical Testing of Nonoxynol-9 as Potential Anti-Human Immunodeficiency Virus Microbicide: a Retrospective Analysis of Results from Five Laboratories

FDA Public Meeting Report on “Drug Interactions With Hormonal Contraceptives: Public Health and Drug Development Implications”

A Summary of the Sixth International Workshop on Microbiome in HIV Pathogenesis, Prevention, and Treatment

Considerations and development of topical microbicides to inhibit the sexual transmission of HIV

Functional homologs of cyanovirin-N amenable to mass production in prokaryotic and eukaryotic hosts

The next generation of HIV/AIDS drugs: novel and developmental antiHIV drugs and targets

The Biological Effects of Structural Variation at the Meta Position of the Aromatic Rings and at the End of the Alkenyl Chain in the Alkenyldiarylmethane Series of Non-Nucleoside Reverse Transcriptase Inhibitors

Outcomes of a National Institute of Allergy and Infectious Diseases Workshop on understanding HIV-exposed but seronegative individuals

Solid-Phase Synthesis of the Alkenyldiarylmethane (ADAM) Series of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

Synthesis and anti-HIV activity of a bile acid analog of cosalane

Inhibition of Acute-, Latent-, and Chronic-Phase Human Immunodeficiency Virus Type 1 (HIV-1) Replication by a Bistriazoloacridone Analog That Selectively Inhibits HIV-1 Transcription

Chicoric Acid Analogues as HIV-1 Integrase Inhibitors

Benzamide-Based Thiolcarbamates: A New Class of HIV-1 NCp7 Inhibitors

Antiviral activity of hop constituents against a series of DNA and RNA viruses

Anti-HIV Agents That Selectively Target Retroviral Nucleocapsid Protein Zinc Fingers without Affecting Cellular Zinc Finger Proteins

Metal-Dependent Inhibition of HIV-1 Integrase

Synthesis and Biological Properties of Novel Pyridinioalkanoyl Thiolesters (PATE) as Anti-HIV-1 Agents That Target the Viral Nucleocapsid Protein Zinc Fingers

Optimization of unique, uncharged thioesters as inhibitors of HIV replication

The Secondary Amine/Nitric Oxide Complex Ion R2N[N(O)NO]- as Nucleophile and Leaving Group in SNAr Reactions

SJ-3366, a Unique and Highly Potent Nonnucleoside Reverse Transcriptase Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1) That Also Inhibits HIV-2

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