Inhibition of HSV-1 protease by benzoxazinones-Reference-Cited by-同舟云学术

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Inhibition of HSV-1 protease by benzoxazinones

Published:1996-10 Issue:20 Volume:6 Page:2463-2466
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Jarvest Richard L.,Parratt Martin J.,Debouck Christine M.,Gorniak Joselina G.,John Jennings L.,Serafinowska Halina T.,Strickler James E.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

1. The herpes simplex virus 1 gene encoding a protease also contains within its coding domain the gene encoding the more abundant substrate.

2. The protease of herpes simplex virus type 1 is essential for functional capsid formation and viral growth

3. Identification of the serine residue at the active site of the herpes simplex virus type 1 protease.

4. A new class of heterocyclic serine protease inhibitors. Inhibition of human leukocyte elastase, porcine pancreatic elastase, cathepsin G, and bovine chymotrypsin A alpha with substituted benzoxazinones, quinazolines, and anthranilates.

5. Suicide inactivation of chymotrypsin by benzoxazinones

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