Publikation: Nitroimidazoles Part 7 : Synthesis and Anti-HIV Activity of New 4-Nitroimidazole Derivatives
Lade...
Dateien
Zu diesem Dokument gibt es keine Dateien.
Datum
2012
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Zeitschriftenartikel
Publikationsstatus
Published
Erschienen in
Zeitschrift für Naturforschung B. 2012, 67(8). ISSN 1865-7117. Available under: doi: 10.5560/ZNB.2012-0122
Zusammenfassung
Reverse transcriptase enzyme (RT) is an attractive target for the development of new drugs useful in AIDS therapy and HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs), and offers the possibility of generating structures of increased potency. On this basis, a series of 4-oxo-3-phenyl-2-(phenylimino)thiazolidin-5-ylidene, 3-hydroxypropyl, 3-azidopropyl, and 3-aminopropyl derivatives of 1-benzyl-2-ethyl-4-nitroimidazoles 6–8, as well as the substituted 1,2,3-triazolo analogs 12–14, the diazepam 15 and carboxamide derivatives 16 and 17 were synthesized. All compounds have been evaluated for their anti-HIV activity.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
540 Chemie
Schlagwörter
Anti-HIV activity, Nitroimidazoles, NNRTIs, Piperazine Derivatives
Konferenz
Rezension
undefined / . - undefined, undefined
Zitieren
ISO 690
AL-MASOUDI, Najim A., Wolfgang PFLEIDERER, Christophe PANNECOUQUE, 2012. Nitroimidazoles Part 7 : Synthesis and Anti-HIV Activity of New 4-Nitroimidazole Derivatives. In: Zeitschrift für Naturforschung B. 2012, 67(8). ISSN 1865-7117. Available under: doi: 10.5560/ZNB.2012-0122BibTex
@article{AlMasoudi2012Nitro-22647,
year={2012},
doi={10.5560/ZNB.2012-0122},
title={Nitroimidazoles Part 7 : Synthesis and Anti-HIV Activity of New 4-Nitroimidazole Derivatives},
number={8},
volume={67},
issn={1865-7117},
journal={Zeitschrift für Naturforschung B},
author={Al-Masoudi, Najim A. and Pfleiderer, Wolfgang and Pannecouque, Christophe}
}RDF
<rdf:RDF
xmlns:dcterms="http://purl.org/dc/terms/"
xmlns:dc="http://purl.org/dc/elements/1.1/"
xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
xmlns:bibo="http://purl.org/ontology/bibo/"
xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
xmlns:foaf="http://xmlns.com/foaf/0.1/"
xmlns:void="http://rdfs.org/ns/void#"
xmlns:xsd="http://www.w3.org/2001/XMLSchema#" >
<rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/22647">
<dc:creator>Pfleiderer, Wolfgang</dc:creator>
<dcterms:bibliographicCitation>Zeitschrift für Naturforschung B ; 67b (2012), 8. - S. 835-842</dcterms:bibliographicCitation>
<dc:creator>Pannecouque, Christophe</dc:creator>
<dc:contributor>Al-Masoudi, Najim A.</dc:contributor>
<void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
<dcterms:title>Nitroimidazoles Part 7 : Synthesis and Anti-HIV Activity of New 4-Nitroimidazole Derivatives</dcterms:title>
<dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
<dc:contributor>Pfleiderer, Wolfgang</dc:contributor>
<dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
<dcterms:abstract xml:lang="eng">Reverse transcriptase enzyme (RT) is an attractive target for the development of new drugs useful in AIDS therapy and HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs), and offers the possibility of generating structures of increased potency. On this basis, a series of 4-oxo-3-phenyl-2-(phenylimino)thiazolidin-5-ylidene, 3-hydroxypropyl, 3-azidopropyl, and 3-aminopropyl derivatives of 1-benzyl-2-ethyl-4-nitroimidazoles 6–8, as well as the substituted 1,2,3-triazolo analogs 12–14, the diazepam 15 and carboxamide derivatives 16 and 17 were synthesized. All compounds have been evaluated for their anti-HIV activity.</dcterms:abstract>
<dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-05-06T13:31:30Z</dcterms:available>
<dc:contributor>Pannecouque, Christophe</dc:contributor>
<bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/22647"/>
<dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/>
<foaf:homepage rdf:resource="http://localhost:8080/"/>
<dc:creator>Al-Masoudi, Najim A.</dc:creator>
<dc:rights>terms-of-use</dc:rights>
<dcterms:issued>2012</dcterms:issued>
<dc:language>eng</dc:language>
<dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-05-06T13:31:30Z</dc:date>
</rdf:Description>
</rdf:RDF>