Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-1-Reference-Cited by-同舟云学术

Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-1

Published:2016-09-22 Issue:19 Volume:59 Page:9262-9268
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Zhao Yu¹,Gu Qiong¹²,Morris-Natschke Susan L.¹,Chen Chin-Ho³,Lee Kuo-Hsiung¹⁴

Affiliation:

1. Natural Products Research Laboratories, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599-7568, United States

2. Research Center for Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, People’s Republic of China

3. Surgical Oncology Research Facility, Duke University Medical Center, Box 2926, Durham, North Carolina 27710, United States

4. Chinese Medicine Research and Development Center, China Medical University and Hospital, 404 Taichung, Taiwan

Funder

National Institute of Allergy and Infectious Diseases

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.6b00461

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4. Anti-AIDS Agents, 11. Betulinic Acid and Platanic Acid as Anti-HIV Principles from Syzigium claviflorum, and the Anti-HIV Activity of Structurally Related Triterpenoids

5. Betulinic Acid and Dihydrobetulinic Acid Derivatives as Potent Anti-HIV Agents

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