Design, Synthesis, and Antiviral Activity of the Thiazole Positional Isomers of a Potent HIV‐1 Entry Inhibitor NBD‐14270-Reference-Cited by-同舟云学术

Design, Synthesis, and Antiviral Activity of the Thiazole Positional Isomers of a Potent HIV‐1 Entry Inhibitor NBD‐14270

Published:2022-09-29 Issue:22 Volume:17 Page:
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Kurkin Alexander V.¹,Curreli Francesca²,Iusupov Ildar R.¹,Spiridonov Evgeniy A.¹,Ahmed Shahad²,Markov Pavel O.¹,Manasova Ekaterina V.¹,Altieri Andrea¹,Debnath Asim K.²^ORCID

Affiliation:

1. EDASA Scientific srls Via Stingi 37 66050 San Salvo (CH) Italy

2. Laboratory of Molecular Modeling & Drug Design Lindsley F. Kimball Research Institute New York Blood Center 310 E 67th Street New York NY 10065 USA

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cmdc.202200344

Reference38 articles.

1. Enfuvirtide: A Novel Agent for the Treatment of HIV-1 Infection

2. Enfuvirtide, a New Fusion Inhibitor for Therapy of Human Immunodeficiency Virus Infection

3. Maraviroc (UK-427,857), a Potent, Orally Bioavailable, and Selective Small-Molecule Inhibitor of Chemokine Receptor CCR5 with Broad-Spectrum Anti-Human Immunodeficiency Virus Type 1 Activity

4. Maraviroc, a CCR5 Coreceptor Antagonist That Blocks Entry of Human Immunodeficiency Virus Type 1

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