Design and Synthesis of P1–P3 Macrocyclic Tertiary-Alcohol-Comprising HIV-1 Protease Inhibitors-Reference-Cited by-同舟云学术

Design and Synthesis of P1–P3 Macrocyclic Tertiary-Alcohol-Comprising HIV-1 Protease Inhibitors

Published:2013-11-11 Issue:22 Volume:56 Page:8999-9007
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Joshi Advait¹,Véron Jean-Baptiste¹,Unge Johan²,Rosenquist Åsa³,Wallberg Hans³,Samuelsson Bertil³,Hallberg Anders¹,Larhed Mats¹

Affiliation:

1. Department of Medicinal Chemistry, Organic Pharmaceutical Chemistry, BMC, Uppsala University, P.O. Box 574, SE-751 23 Uppsala, Sweden

2. MAX IV-laboratory, Lund University, P.O. Box 118, SE-221 00 Lund, Sweden

3. Medivir AB, P.O. Box 1086, SE-141 22 Huddinge, Sweden

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm400811d

Reference33 articles.

1. Inhibitors of HIV-1 Protease: Current State of the Art 10 Years After their Introduction. From Antiretroviral Drugs to Antifungal, Antibacterial and Antitumor Agents Based on Aspartic Protease Inhibitors

2. Understanding and managing the adverse effects of antiretroviral therapy

3. FDA list of antiretroviral drugs used in the treatment of HIV infection.http://www.fda.gov/ForConsumers/byAudience/ForPatientAdvocates/HIVandAIDSActivities/ucm118915.htm

4. Lopinavir-Ritonavir: A New Protease Inhibitor

5. Tipranavir

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