Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents-Reference-Cited by-同舟云学术

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Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents

Published:1999-11 Issue:22 Volume:9 Page:3217-3220
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Patel Mona,Rodgers James D.,McHugh Robert J.,Johnson Barry L.,Cordova Beverly C.,Klabe Ronald M.,Bacheler Lee T.,Erickson-Viitanen Susan,Ko Soo S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. Potent cyclic urea HIV protease inhibitors with benzofused heterocycles as P2/P2′ groups

2. Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2′ groups

3. Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors

4. Nonsymmetric P2/P2‘ Cyclic Urea HIV Protease Inhibitors. Structure−Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues

5. Über Lichtreaktionen, XIX. Photolyse von 3-Diazo-indoleninen und -indazoleninen in verschiedenen Medien

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