Structural Optimization of 2,3-Dihydro-1H-cyclopenta[b]quinolines Targeting the Noncatalytic RVxF Site of Protein Phosphatase 1 for HIV-1 Inhibition-Reference-Cited by-同舟云学术

Structural Optimization of 2,3-Dihydro-1H-cyclopenta[b]quinolines Targeting the Noncatalytic RVxF Site of Protein Phosphatase 1 for HIV-1 Inhibition

Published:2020-12-01 Issue:12 Volume:6 Page:3190-3211
ISSN:2373-8227
Container-title:ACS Infectious Diseases
language:en
Short-container-title:ACS Infect. Dis.

Author:

Lin Xionghao¹²,Sajith Ayyiliath M³,Wang Songping¹,Kumari Namita¹⁴,Choy Meng S⁵,Ahmad Asrar¹,Cadet Dana R.⁶,Gu Xinbin²,Ivanov Andrey I.¹,Peti Wolfgang⁵^ORCID,Kulkarni Amol³,Nekhai Sergei¹⁴^ORCID

Affiliation:

1. Center for Sickle Cell Disease, College of Medicine, Howard University, Washington, DC 20059, United States

2. Department of Oral Pathology, College of Dentistry, Howard University, Washington, DC 20059, United States

3. Department of Pharmaceutical Sciences, College of Pharmacy, Howard University, Washington, DC 20059, United States

4. Department of Medicine, College of Medicine, Howard University, Washington, DC 20059 United States

5. Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721 United States

6. Department of Natural Science, Bowie State University, Bowie, Maryland 20715, United States

Funder

National Heart, Lung, and Blood Institute

National Institute of Dental and Craniofacial Research

National Institute of Allergy and Infectious Diseases

National Institute on Minority Health and Health Disparities

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Infectious Diseases

Link

https://pubs.acs.org/doi/pdf/10.1021/acsinfecdis.0c00511

Reference27 articles.

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2. Cat and Mouse: HIV Transcription in Latency, Immune Evasion and Cure/Remission Strategies

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