Literature DB >> 25313716

Novel HIV-1 non-nucleoside reverse transcriptase inhibitors: a patent review (2011-2014).

Xiao Li1, Lingzi Zhang, Ye Tian, Yu'ning Song, Peng Zhan, Xinyong Liu.   

Abstract

INTRODUCTION: There is a continuous need for next-generation non-nucleoside RT inhibitors (NNRTIs) with different resistance profiles, improved safety, excellent tolerability, and favorable physicochemical properties. AREAS COVERED: In this review we intend to narrate a general and cutting-edge overview of current state of NNRTI patents during the 2011-2014 (June) period and future perspectives. Particular focus is placed on the highlighting of some emerging medicinal chemistry principles and insights in the discovery and development of NNRTIs. EXPERT OPINION: The development of effective NNRTIs is moving on from trial-and-error approaches to sophisticated subconscious strategies. Several newly emerging structure-based virtual screening methodologies (such as Monte Carlo free energy perturbation calculations) or new drug design insights, such as taking full use of the specific noncovalent reverse transcriptase/NNRTIs interactions, stereochemical diversity-oriented conformational restriction, novel strategies to enhance solubility and early absorption, distribution, metabolism, excretion, and toxicity (ADMET) assessment, will continue to evolve to complement the classical NNRTIs discovery approaches (structure-based core-refining and substituents-decorating).

Entities:  

Keywords:  AIDS; HIV-1; drug design; inhibitor; medicinal chemistry; non-nucleoside RT inhibitors; patent; reverse transcriptase

Mesh:

Substances:

Year:  2014        PMID: 25313716     DOI: 10.1517/13543776.2014.964685

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  5 in total

1.  FRET-based assay to screen inhibitors of HIV-1 reverse transcriptase and nucleocapsid protein.

Authors:  Kamal K Sharma; Frédéric Przybilla; Tobias Restle; Julien Godet; Yves Mély
Journal:  Nucleic Acids Res       Date:  2016-01-13       Impact factor: 16.971

2.  Diaryl ethers with carboxymethoxyphenacyl motif as potent HIV-1 reverse transcriptase inhibitors with improved solubility.

Authors:  Tomasz Frączek; Rafał Kamiński; Agnieszka Krakowiak; Evelien Naessens; Bruno Verhasselt; Piotr Paneth
Journal:  J Enzyme Inhib Med Chem       Date:  2018-12       Impact factor: 5.051

3.  First discovery of novel 3-hydroxy-quinazoline-2,4(1H,3H)-diones as specific anti-vaccinia and adenovirus agents via 'privileged scaffold' refining approach.

Authors:  Dongwei Kang; Heng Zhang; Zhongxia Zhou; Boshi Huang; Lieve Naesens; Peng Zhan; Xinyong Liu
Journal:  Bioorg Med Chem Lett       Date:  2016-09-29       Impact factor: 2.823

4.  Pyrimidine 2,4-Diones in the Design of New HIV RT Inhibitors.

Authors:  Roberto Romeo; Daniela Iannazzo; Lucia Veltri; Bartolo Gabriele; Beatrice Macchi; Caterina Frezza; Francesca Marino-Merlo; Salvatore V Giofrè
Journal:  Molecules       Date:  2019-05-02       Impact factor: 4.411

5.  Screening and Evaluation of Novel Compounds against Hepatitis B Virus Polymerase Using Highly Purified Reverse Transcriptase Domain.

Authors:  Eriko Ohsaki; Keiji Ueda
Journal:  Viruses       Date:  2020-07-31       Impact factor: 5.048

  5 in total

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