Antiviral drug discovery and development: where chemistry meets with biomedicine.

Abstract:

:The successful development of antiviral drugs is highly dependent on a close interaction and collaboration between the chemist and the biologist (biomedic). This is illustrated by a number of representative examples: S-adenosylhomocysteine (SAH) hydrolase inhibitors which display broad-spectrum antiviral activity, bromovinyldeoxyuridine (BVDU) and derivatives thereof, that are highly selective inhibitors of varicella-zoster virus (VZV), (dideoxy)nucleoside reverse transcriptase inhibitors (NRTIs) and non-nucleoside reverse transcriptase inhibitors (NNRTIs) which are now widely used in the treatment of HIV infections (AIDS), the bicyclams (i.e. AMD3100) which were originally discovered as anti-HIV agents, then found to be potent CXCR4 antagonists and now being pursued for a number of indications such as stem cell mobilization, and the acyclic nucleoside phosphonates which have heralded a new strategy for the treatment of various DNA virus (herpes-, adeno-, pox-, papillomavirus) infections (cidofovir), hepatitis B (adefovir) and AIDS (tenofovir).

journal_name

Antiviral Res

journal_title

Antiviral research

authors

De Clercq E

doi

10.1016/j.antiviral.2005.05.001

subject

Has Abstract

pub_date

2005-08-01 00:00:00

pages

56-75

issue

2

eissn

0166-3542

issn

1872-9096

pii

S0166-3542(05)00113-0

journal_volume

67

pub_type

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