Viral proteases as targets for drug design.

Abstract:

:In order to productively infect a host, viruses must enter the cell and force host cell replication mechanisms to produce new infectious virus particles. The success of this process unfortunately results in disease progression and, in the case of infection with many viral species, may cause mortality. The discoveries of Louis Pasteur and Edward Jenner led to one of the greatest advances in modern medicine - the development of vaccines that generate long-lasting memory immune responses to combat viral infection. Widespread use of vaccines has reduced mortality and morbidity associated with viral infection and, in some cases, has completely eradicated virus from the human population. Unfortunately, several viral species maintain a significant ability to mutate and "escape" vaccine-induced immune responses. Thus, novel anti-viral agents are required for treatment and prevention of viral disease. Targeting proteases that are crucial in the viral life cycle has proven to be an effective method to control viral infection, and this avenue of investigation continues to generate anti-viral treatments. Herein, we provide the reader with a brief history as well as a comprehensive review of the most recent advances in the design and synthesis of viral protease inhibitors.

journal_name

Curr Pharm Des

authors

Skoreński M,Sieńczyk M

doi

10.2174/1381612811319060013

subject

Has Abstract

pub_date

2013-01-01 00:00:00

pages

1126-53

issue

6

eissn

1381-6128

issn

1873-4286

pii

CPD-EPUB-20120918-24

journal_volume

19

pub_type

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