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Developments in antiviral drug design, discovery and development in 2004.

Identifieur interne : 004864 ( Main/Exploration ); précédent : 004863; suivant : 004865

Developments in antiviral drug design, discovery and development in 2004.

Auteurs : Nicholas A. Meanwell [États-Unis] ; Makonen Belema ; David J. Carini ; Stanley V. D'Andrea ; John F. Kadow ; Mark Krystal ; B Narasimhulu Naidu ; Alicia Regueiro-Ren ; Paul M. Scola ; Sing-Yuen Sit ; Michael A. Walker ; Tao Wang ; Kap-Sun Yeung

Source :

RBID : pubmed:16535860

Descripteurs français

English descriptors

Abstract

This article summarizes key aspects of progress made during 2004 toward the design, discovery and development of antiviral agents for clinical use. Important developments in the identification, characterization and clinical utility of inhibitors of human immunodeficiency virus; the hepatitis viruses, hepatitis B, hepatitis C; the herpes family of viruses, herpes simplex viruses 1 and 2, varicella zoster virus, Epstein-Barr virus and human cytomegalovirus; the respiratory viruses, influenza, respiratory syncytial virus, human metapneumovirus, picornaviruses, measles and the severe acute respiratory syndrome coronavirus; human papilloma virus; rotavirus; Ebola virus and West Nile virus, are reviewed.

DOI: 10.2174/156800505774912893
PubMed: 16535860


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Antiviral Agents (pharmacology)</term>
<term>Clinical Trials as Topic</term>
<term>Drug Design</term>
<term>Drug Evaluation, Preclinical</term>
<term>HIV Integrase Inhibitors (chemistry)</term>
<term>HIV Integrase Inhibitors (pharmacology)</term>
<term>HIV-1 (drug effects)</term>
<term>HIV-2 (drug effects)</term>
<term>Hepatitis Viruses (drug effects)</term>
<term>Herpesviridae (drug effects)</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Molecular Structure</term>
<term>Nucleic Acid Synthesis Inhibitors</term>
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<term>Nucleosides (pharmacology)</term>
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<term>Protease Inhibitors (chemistry)</term>
<term>Protease Inhibitors (pharmacology)</term>
<term>Reverse Transcriptase Inhibitors (chemistry)</term>
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<term>Antiviraux (pharmacologie)</term>
<term>Conception de médicament</term>
<term>Données de séquences moléculaires</term>
<term>Essais cliniques comme sujet</term>
<term>Herpesviridae ()</term>
<term>Humains</term>
<term>Inhibiteurs de l'intégrase du VIH ()</term>
<term>Inhibiteurs de l'intégrase du VIH (pharmacologie)</term>
<term>Inhibiteurs de la synthèse d'acide nucléique</term>
<term>Inhibiteurs de la transcriptase inverse ()</term>
<term>Inhibiteurs de la transcriptase inverse (pharmacologie)</term>
<term>Inhibiteurs de protéases ()</term>
<term>Inhibiteurs de protéases (pharmacologie)</term>
<term>Nucléosides ()</term>
<term>Nucléosides (pharmacologie)</term>
<term>Orthomyxoviridae ()</term>
<term>Structure moléculaire</term>
<term>Séquence d'acides aminés</term>
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<term>Virus du SRAS ()</term>
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<div type="abstract" xml:lang="en">This article summarizes key aspects of progress made during 2004 toward the design, discovery and development of antiviral agents for clinical use. Important developments in the identification, characterization and clinical utility of inhibitors of human immunodeficiency virus; the hepatitis viruses, hepatitis B, hepatitis C; the herpes family of viruses, herpes simplex viruses 1 and 2, varicella zoster virus, Epstein-Barr virus and human cytomegalovirus; the respiratory viruses, influenza, respiratory syncytial virus, human metapneumovirus, picornaviruses, measles and the severe acute respiratory syndrome coronavirus; human papilloma virus; rotavirus; Ebola virus and West Nile virus, are reviewed.</div>
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