Multi-Substituted Quinolines as HIV-1 Integrase Allosteric Inhibitors (original) (raw)

Structural and theoretical studies of [6-bromo-1-(4-fluorophenylmethyl)-4(1H)-quinolinon-3-yl)]-4-hydroxy-2-oxo-3-butenoïc acid as HIV-1 integrase inhibitor

Laszlo Hevesi

Bioorganic & Medicinal Chemistry Letters, 2009

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Linker-modified quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity

Didier Desmaële

Bioorganic & Medicinal Chemistry Letters, 2004

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HIV-1 integrase tetramers are the antiviral target of pyridine-based allosteric integrase inhibitors

Ashwanth Francis

eLife

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Discovery of a Distinct Chemical and Mechanistic Class of Allosteric HIV-1 Integrase Inhibitors with Antiretroviral Activity

Antonella Converso

ACS chemical biology, 2017

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Development of an AlphaScreen-Based HIV-1 Integrase Dimerization Assay for Discovery of Novel Allosteric Inhibitors

Maurizio Botta

Journal of Biomolecular Screening, 2012

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New Class of HIV-1 Integrase (IN) Inhibitors with a Dual Mode of Action

Roman Sakowicz

Journal of Biological Chemistry, 2012

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Novel bifunctional quinolonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, biological activities, and mechanism of action

Antonio Lavecchia

2006

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Progress in HIV-1 Integrase Inhibitors: A Review of their Chemical Structure Diversity

zahra hajimahdi

Iranian journal of pharmaceutical research : IJPR, 2016

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Preclinical Profile of BI 224436, a Novel HIV-1 Non-Catalytic Site Integrase Inhibitor

Stephen Kawai

Antimicrobial Agents and Chemotherapy, 2014

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Discovery of BI 224436, a Noncatalytic Site Integrase Inhibitor (NCINI) of HIV-1

Punit Bhardwaj

ACS Medicinal Chemistry Letters, 2014

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Novel HIV-1 Integrase Inhibitors Derived from Quinolone Antibiotics

Nnamdi Mcben

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Design and Development of Integrase Inhibitors as Anti-HIV Agents

A. Nagappa

Current Medicinal Chemistry, 2003

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Novel Quinolinonyl Diketo Acid Derivatives as HIV-1 Integrase Inhibitors: Design, Synthesis, and Biological Activities

Antonio Lavecchia

Journal of Medicinal Chemistry, 2008

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Kuwanon-L as a new allosteric HIV-1 integrase inhibitor: molecular modeling and biological evaluation

Francesca Esposito, Valentina Iovine, R. Ferrarese, F. Canducci, Angela Corona, Andrea Calcaterra

Chembiochem : a European journal of chemical biology, 2015

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A unique conformational escape reaction of HIV-1 against an allosteric integrase inhibitor

Masayuki Amano

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A Versatile and Practical Synthesis toward the Development of Novel HIV-1 Integrase Inhibitors

Giulia Vignaroli

ChemMedChem, 2011

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Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: A platform for antiviral drug design

Yehuda Goldgur

Proceedings of the National Academy of Sciences, 1999

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Toward novel HIV1 integrase binding inhibitors: Molecular modeling, synthesis, and biological studies

Suvi Rajamaki

Bioorganic & Medicinal Chemistry Letters, 2007

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Styrylquinoline Derivatives: A New Class of Potent HIV-1 Integrase Inhibitors That Block HIV-1 Replication in CEM Cells

Christian Auclair

Journal of Medicinal Chemistry, 1998

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HIV1 integrase strand-transfer inhibitors: Design, synthesis and molecular modeling investigation

Laura De Luca

European Journal of Medicinal Chemistry, 2011

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A QSAR Study on Some Series of HIV-1 Integrase Inhibitors

Shikha Kaushik

Medicinal Chemistry, 2011

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Study of inhibitory mechanism and binding mode of the thiazolo quinazoline compounds to HIV-1 integrase by docking

Arvind Kumar

2010

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A refined pharmacophore model for HIV1 integrase inhibitors: Optimization of potency in the 1H-benzylindole series

Laura Luca

Bioorganic & Medicinal Chemistry Letters, 2008

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