Synthesis and evaluation of substituted 4-arylimino-3-hydroxybutanoic acids as potential HIV-1 integrase inhibitors-Reference-Cited by-同舟云学术

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Synthesis and evaluation of substituted 4-arylimino-3-hydroxybutanoic acids as potential HIV-1 integrase inhibitors

Published:2018-04 Issue:6 Volume:28 Page:1067-1070
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Faridoon ,Mnkandhla Dumisani,Isaacs Michelle,Hoppe Heinrich C.,Kaye Perry T.

Funder

SAMRC

Economic Competitiveness and Support Package

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. Synthesis, docking, and biological studies of phenanthrene β-diketo acids as novel HIV-1 integrase inhibitors;Sharma;Bioorg Med Chem Lett,2013

2. Synthesis of dihydropyrimidine α,γ-diketobutanoic acid derivatives targeting HIV integrase;Sari;Eur J Med Chem,2015

3. Maraviroc: The first of a new class of antiretroviral agents;MacArthur;Clin Infect Dis,2008

4. HIV-1 in strand transfer chelating inhibitors: a focus on metal binding;Bacchi;Mol Pharm,2011

5. Integrase inhibitors to treat HIV/Aids;Pommier;Nat Rev Drug Discov,2005

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3. ENVIRONMENTALLY BENIGN SYNTHESIS OF NEW 1,3-OXAZOLIDINES AND AZOMETHYNES ON THE BASE OF ARYLAMINOPROPANOLS;REV ROUM CHIM;2021

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