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Discovery and Development of GS 4104 (oseltamivir) An Orally Active Influenza Neuraminidase Inhibitor
- Source :
- Current Medicinal Chemistry. 7:663-672
- Publication Year :
- 2000
- Publisher :
- Bentham Science Publishers Ltd., 2000.
-
Abstract
- Rational drug design utilizing available X-ray crystal structures of sialic acid analogues bound to the active site of influenza virus neuraminidase has led to the discovery of a series of potent carbocyclic influenza neuraminidase inhibitors. From this series, GS 4104 (oseltamivir, TAMIFLU) has emerged as a promising antiviral for the treatment and prophylaxis of human influenza infection. This article will summarize the design, discovery, and development of oseltamivir as an oral therapeutic to treat influenza infection.
- Subjects :
- Oseltamivir
Orthomyxoviridae
Administration, Oral
Neuraminidase
Drug design
Antiviral Agents
Biochemistry
Virus
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
Animals
Humans
Amines
Enzyme Inhibitors
Pharmacology
biology
Organic Chemistry
virus diseases
Prodrug
biology.organism_classification
Virology
Sialic acid
chemistry
Enzyme inhibitor
Drug Design
Immunology
biology.protein
Molecular Medicine
Subjects
Details
- ISSN :
- 09298673
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- Current Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....5f27ea5a5f6ad9d8f935375ec560b2c8
- Full Text :
- https://doi.org/10.2174/0929867003374886