Structural exploration of hydroxyethylamines as HIV-1 protease inhibitors: new features identified-Reference-Cited by-同舟云学术

Structural exploration of hydroxyethylamines as HIV-1 protease inhibitors: new features identified

Published:2018-03-23 Issue:5 Volume:29 Page:385-408
ISSN:1062-936X
Container-title:SAR and QSAR in Environmental Research
language:en
Short-container-title:SAR and QSAR in Environmental Research

Author:

Amin S. A.¹^ORCID,Adhikari N.¹^ORCID,Bhargava S.²,Jha T.¹^ORCID,Gayen S.²

Affiliation:

1. Natural science Laboratory, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, P.O. Box 17020, Jadavpur University , Kolkata 700032, West Bengal, India

2. Laboratory of Drug Design and Discovery, Department of Pharmaceutical Sciences, Dr Hari Singh Gour University , Sagar 470003, Madhya Pradesh, India

Publisher

Informa UK Limited

Subject

Drug Discovery,Molecular Medicine,General Medicine,Bioengineering

Link

https://www.tandfonline.com/doi/pdf/10.1080/1062936X.2018.1447511

Reference45 articles.

1. Design and Development of Highly Potent HIV-1 Protease Inhibitors with a Crown-Like Oxotricyclic Core as the P2-Ligand To Combat Multidrug-Resistant HIV Variants

2. Recent Progress in the Development of HIV-1 Protease Inhibitors for the Treatment of HIV/AIDS

3. Twenty-Six Years of Anti-HIV Drug Discovery: Where Do We Stand and Where Do We Go?

4. Investigational protease inhibitors as antiretroviral therapies

5. Anti-HIV Drug Discovery and Development: Current Innovations and Future Trends

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