Design and synthesis of monocyclic β-lactams as mechanism-based inhibitors of human cytomegalovirus protease-Reference-Cited by-同舟云学术

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Design and synthesis of monocyclic β-lactams as mechanism-based inhibitors of human cytomegalovirus protease

Published:1998-02 Issue:4 Volume:8 Page:365-370
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Borthwick Alan D.,Weingarten Gordon,Haley Terry M.,Tomaszewski Mirek,Wang Wei,Hu Zhouhan,Bedard Jean,Jin Haloun,Yuen Leonard,Mansour Tarek S.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

1. Assemblin, a herpes virus serine maturational proteinase and new molecular target for antivirals

2. Herpesvirus proteases: targets for novel antiviral drugs

3. Structure of the Human Cytomegalovirus Protease Catalytic Domain Reveals a Novel Serine Protease Fold and Catalytic Triad

4. A new serine-protease fold revealed by the crystal structure of human cytomegalovirus protease

5. Unique fold and active site in cytomegalovirus protease

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1. Synthesis, characterization, and biological activity using computational study of synthesized monocyclic β-lactam ligands;2024-05-09

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5. Synthesis, Characterization, and Biological Activity Using Computational Study of Synthesized Monocyclic Β-Lactam Ligands;2024

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