Design and Synthesis of New Potent C2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold-Reference-Cited by-同舟云学术

Design and Synthesis of New Potent C2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold

Published:1998-08-26 Issue:20 Volume:41 Page:3782-3792
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Alterman Mathias¹,Björsne Magnus¹,Mühlman Anna¹,Classon Björn¹,Kvarnström Ingemar¹,Danielson Helena¹,Markgren Per-Olof¹,Nillroth Ulrika¹,Unge Torsten¹,Hallberg Anders¹,Samuelsson Bertil¹

Affiliation:

1. Department of Chemistry, Linköping University, S-581 83 Linköping, Sweden, Arrhenius Laboratory, Department of Organic Chemistry, Stockholm University, S-106 91 Stockholm, Sweden, Department of Biochemistry, Uppsala University, BMC, S-751 23 Uppsala, Sweden, Department of Molecular Biology, Uppsala University, BMC, Box 590, S-751 24 Uppsala, Sweden, and Department of Organic Pharmaceutical Chemistry, Uppsala University, BMC, S-751 23 Uppsala, Sweden

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm970777b

Reference50 articles.

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

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

3. Isolation of a New Human Retrovirus from West African Patients with AIDS

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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