(Iso)Quinoline-Artemisinin Hybrids Prepared through Click Chemistry: Highly Potent Agents against Viruses.


Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
16 Sep 2020
Historique:
received: 14 04 2020
pubmed: 3 6 2020
medline: 25 2 2021
entrez: 3 6 2020
Statut: ppublish

Résumé

Viral infections cause life-threatening diseases in millions of people worldwide every year and there is an urgent need for new, effective antiviral drugs. Hybridization of two chemically diverse compounds into a new bioactive effector product is a successful concept to improve the properties of a hybrid drug relative to the parent compounds. In this study, (iso)quinoline-artemisinin hybrids, obtained through copper-catalyzed azide-alkyne cycloaddition or metal-free click reactions (in organic solvents or in the presence of water), were analyzed in vitro, for the first time, for their inhibitory activity against human cytomegalovirus (HCMV), relative to their parent compounds and the reference drug ganciclovir. EC

Identifiants

pubmed: 32485071
doi: 10.1002/chem.202001803
pmc: PMC7540715
doi:

Substances chimiques

Antiviral Agents 0
Artemisinins 0
Quinolines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12019-12026

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : TS 87/16-3
Organisme : Deutsche Forschungsgemeinschaft
ID : MM 1289/7-1/7-3
Organisme : Deutsche Forschungsgemeinschaft
ID : MM 1289/11-1
Organisme : Deutsche Forschungsgemeinschaft
ID : GRK 2504 (A1/MM)
Organisme : Deutsche Forschungsgemeinschaft
ID : Gottfried Wilhelm Leibniz award
Organisme : Deutscher Akademischer Austauschdienst
Organisme : Alexander von Humboldt-Stiftung
Organisme : ERDF/ESF
ID : ChemBioDrug CZ.02.1.01/0.0/0.0/16_019/0000729

Informations de copyright

© 2020 The Authors. Published by Wiley-VCH GmbH.

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Auteurs

Aysun Çapcı (A)

Organic Chemistry Chair I and Interdisciplinary Center for, Molecular Materials (ICMM), Friedrich-Alexander University of, Erlangen-Nürnberg, Nikolaus Fiebiger-Straße 10, 91058, Erlangen, Germany.

Mélanie M Lorion (MM)

Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.

Christina Mai (C)

Organic Chemistry Chair I and Interdisciplinary Center for, Molecular Materials (ICMM), Friedrich-Alexander University of, Erlangen-Nürnberg, Nikolaus Fiebiger-Straße 10, 91058, Erlangen, Germany.

Friedrich Hahn (F)

Institute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.

Jan Hodek (J)

Institute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo namesti 2, 16610, Prague, Czech Republic.

Christina Wangen (C)

Institute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.

Jan Weber (J)

Institute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo namesti 2, 16610, Prague, Czech Republic.

Manfred Marschall (M)

Institute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.

Lutz Ackermann (L)

Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
German Center for Cardiovascular Research (DZHK), Potsdamer Str. 58, 10785, Berlin, Germany.

Svetlana B Tsogoeva (SB)

Organic Chemistry Chair I and Interdisciplinary Center for, Molecular Materials (ICMM), Friedrich-Alexander University of, Erlangen-Nürnberg, Nikolaus Fiebiger-Straße 10, 91058, Erlangen, Germany.

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