The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase-Reference-Cited by-同舟云学术

The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase

Published:2010-03 Issue:6 Volume:20 Page:1994-2000
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Tanis Steven P.,Strohbach Joseph W.,Parker Timothy T.,Moon Malcom W.,Thaisrivongs Suvit,Perrault William R.,Hopkins Todd A.,Knechtel Mary L.,Oien Nancee L.,Wieber Janet L.,Stephanski Kevin J.,Wathen Michael W.

Publisher

Elsevier BV

Subject

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

Reference37 articles.

1. Current and potential therapies for the treatment of herpesvirus infections

2. Non-nucleoside inhibitors of herpesviruses

3. Broad-spectrum antiviral activity of PNU-183792, a 4-oxo-dihydroquinoline, against human and animal herpesviruses

4. Ganciclovir

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