Design and synthesis of novel P2 substituents in diol-based HIV protease inhibitors-Reference-Cited by-同舟云学术

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Design and synthesis of novel P2 substituents in diol-based HIV protease inhibitors

Published:2010-01 Issue:1 Volume:45 Page:160-170
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Adrian Meredith Jenny,Wallberg Hans,Vrang Lotta,Oscarson Stefan,Parkes Kevin,Hallberg Anders,Samuelsson Bertil

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference56 articles.

1. Isolation of Human T-Cell Leukemia Virus in Acquired Immune Deficiency Syndrome (AIDS)

2. Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS)

3. UNAIDS/WHO, Report on the global AIDS epidemic, ISBN 978 92 9 173711 6.

4. A Synthetic HIV-1 Protease Inhibitor with Antiviral Activity Arrests HIV-Like Particle Maturation

5. Human immunodeficiency virus has an aspartic-type protease that can be inhibited by pepstatin A.

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1. Proteases and HPV-Induced Carcinogenesis;Cancers;2022-06-21

2. Amino Acid and Peptide‐Based Antiviral Agents;ChemMedChem;2021-08-03

3. Recent Advances Towards Treatment of HIV: Synthesis and SAR Studies;Mini-Reviews in Medicinal Chemistry;2021-02-16

4. Design and biological evaluation of novel HIV-1 protease inhibitors with isopropanol as P1′ ligand to enhance binding with S1′ subsite;Bioorganic & Medicinal Chemistry;2020-08

5. Design, synthesis and biological evaluation of HIV-1 protease inhibitors with morpholine derivatives as P2 ligands in combination with cyclopropyl as P1′ ligand;Bioorganic & Medicinal Chemistry Letters;2020-04

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