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Synthesis, antiviral activity, and mechanism of drug resistance of D- and L-2',3'-didehydro-2',3'-dideoxy-2'-fluorocarbocyclic nucleosides

Author
JIANING WANG1 ; YUNHO JIN1 ; RAPP, Kimberly L2 ; BENNETT, Matthew2 ; SCHINAZI, Raymond F2 ; CHU, Chung K1
[1] College of Pharmacy, The University of Georgia, Athens, Georgia 30602, United States
[2] Emory University School of Medicine/Veterans Affairs Medical Center, Atlanta, Georgia 30033, United States
Source

Journal of medicinal chemistry (Print). 2005, Vol 48, Num 11, pp 3736-3748, 13 p ; ref : 22 ref

CODEN
JMCMAR
ISSN
0022-2623
Scientific domain
Pharmacology drugs
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Analogue nucléoside Antiviral Complexe enzyme inhibiteur Composé monocyclique Composé éthylénique Didésoxynucléoside In vitro Lamivudine Mode liaison Modèle moléculaire Modélisation Mécanisme Purine nucléoside Pyrimidine nucléoside Relation structure activité Résistance traitement Site actif Stéréoisomère Synthèse chimique Virus HIV1 Cyclopent-2-èneméthanol dérivé Enzyme Fluor Composé organique Inhibiteur enzyme Inhibiteur reverse transcriptase Lentivirus Nucleotidyltransferases RNA-directed DNA polymerase Retroviridae Transferases Virus immunodéficience humaine Virus
Keyword (en)
Nucleoside analog Antiviral Inhibitor enzyme complex Monocyclic compound Ethylenic compound Dideoxynucleoside In vitro Lamivudine Binding mode Molecular model Modeling Mechanism Purine nucleoside Pyrimidine nucleoside Structure activity relation Treatment resistance Active site Stereoisomer Chemical synthesis HIV-1 virus Enzyme Fluorine Organic compounds Enzyme inhibitor Reverse transcriptase inhibitor Lentivirus Nucleotidyltransferases RNA-directed DNA polymerase Retroviridae Transferases Human immunodeficiency virus Virus
Keyword (es)
Análogo nucleósido Antiviral Complejo enzima inhibidor Compuesto monocíclico Compuesto etilénico Didesoxinucleósido In vitro Lamivudina Modo de enlace Modelo molecular Modelización Mecanismo Purina nucleósido Pirimidina nucleósido Relación estructura actividad Resistencia tratamiento Lugar activo Estereoisómero Síntesis química HIV-1 virus Enzima Fluor Compuesto orgánico Inhibidor enzima Inhibitor reverse transcriptase Lentivirus Nucleotidyltransferases RNA-directed DNA polymerase Retroviridae Transferases Human immunodeficiency virus Virus
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02S Antibiotics. Antiinfectious agents. Antiparasitic agents / 002B02S05 Antiviral agents

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16812137

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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