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A QSAR study on influenza neuraminidase inhibitors.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2006 Feb 15; Vol. 14 (4), pp. 982-96. Date of Electronic Publication: 2005 Oct 06. - Publication Year :
- 2006
-
Abstract
- Influenza is a major respiratory infection associated with significant morbidity in the general population and mortality in elderly and high-risk patients. It is an RNA virus that contains two major surface glycoproteins, neuraminidase and hemagglutinin. These proteins are essential for infection. Neuraminidase has been found to be a potential target to control influenza virus. In this paper, we have developed 17 quantitative structure-activity relationships (QSAR) for different sets of compounds to understand chemical-biological interactions governing their activities toward influenza neuraminidase.
- Subjects :
- Amides chemistry
Antiviral Agents chemistry
Antiviral Agents pharmacology
Benzoic Acid chemistry
Chemical Phenomena
Chemistry, Physical
Cyclopentanes chemistry
Cyclopentanes pharmacology
Isoquinolines chemistry
Isoquinolines pharmacology
Molecular Structure
Neuraminidase metabolism
Pyrrolidines chemistry
Pyrrolidines pharmacology
Quantitative Structure-Activity Relationship
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
Neuraminidase antagonists & inhibitors
Orthomyxoviridae enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 0968-0896
- Volume :
- 14
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 16213733
- Full Text :
- https://doi.org/10.1016/j.bmc.2005.09.016