Privileged Structures Meet Human T-Cell Leukemia Virus-1 (HTLV-1): C2-Symmetric 3,4-Disubstituted Pyrrolidines as Nonpeptidic HTLV-1 Protease Inhibitors-Reference-Cited by-同舟云学术

Privileged Structures Meet Human T-Cell Leukemia Virus-1 (HTLV-1): C2-Symmetric 3,4-Disubstituted Pyrrolidines as Nonpeptidic HTLV-1 Protease Inhibitors

Published:2015-05-22 Issue:11 Volume:58 Page:4845-4850
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Kuhnert Maren¹,Blum Andreas¹,Steuber Holger²,Diederich Wibke E.¹

Affiliation:

1. Institut für Pharmazeutische Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 3, 35043 Marburg, Germany

2. LOEWE-Zentrum für Synthetische Mikrobiologie, Philipps-Universität Marburg, Hans-Meerwein-Straße, 35043 Marburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.5b00346

Reference24 articles.

1. Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma

2. Understanding HTLV-I Protease

3. Crystal structure of human T cell leukemia virus protease, a novel target for anticancer drug design

4. HTLV-1-associated infective dermatitis: updates on the pathogenesis

5. Global epidemic of human T-cell lymphotropic virus type-I (HTLV-I)

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