Cycloalkylpyranones and Cycloalkyldihydropyrones as HIV Protease Inhibitors: Exploring the Impact of Ring Size on Structure−Activity Relationships-Reference-Cited by-同舟云学术

Cycloalkylpyranones and Cycloalkyldihydropyrones as HIV Protease Inhibitors: Exploring the Impact of Ring Size on Structure−Activity Relationships

Published:1996-01-01 Issue:20 Volume:39 Page:4125-4130
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Romines Karen R.¹,Morris Jeanette K.¹,Howe W. Jeffrey¹,Tomich Paul K.¹,Horng Miao-Miao¹,Chong Kong-Teck¹,Hinshaw Roger R.¹,Anderson David J.¹,Strohbach Joseph W.¹,Turner Steve R.¹,Mizsak Steve A.¹

Affiliation:

1. Structural, Analytical and Medicinal Chemistry Research, Computer-Aided Drug Discovery, Chemical and Biological Screening, Cancer and Infectious Diseases Research, and Medicinal Chemistry Research, Pharmacia and Upjohn, Inc., Kalamazoo, Michigan 49001

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm960296c

Reference16 articles.

1. Inhibitors of HIV proteinase

2. Structure-Based Design of HIV Protease Inhibitors: 4-Hydroxycoumarins and 4-Hydroxy-2-pyrones as Non-peptidic Inhibitors

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