Evidence map›Paper›PMID 32485071›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2020

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

Aysun Çapcı, Mélanie M Lorion, Christina Mai, Friedrich Hahn, Jan Hodek, Christina Wangen, Jan Weber, Manfred Marschall, Lutz Ackermann, Svetlana B Tsogoeva

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Aysun ÇapcıOrganic 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 LorionInstitut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Christina MaiOrganic Chemistry Chair I and Interdisciplinary Center for, Molecular Materials (ICMM), Friedrich-Alexander University of, Erlangen-Nürnberg, Nikolaus Fiebiger-Straße 10, 91058, Erlangen, Germany.
Friedrich HahnInstitute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.
Jan HodekInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo namesti 2, 16610, Prague, Czech Republic.
Christina WangenInstitute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.
Jan WeberInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo namesti 2, 16610, Prague, Czech Republic.
Manfred MarschallInstitute for Clinical and Molecular Virology, Friedrich-Alexander University of Erlangen-Nürnberg, Schlossgarten 4, 91054, Erlangen, Germany.
Lutz AckermannInstitut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Svetlana B TsogoevaOrganic Chemistry Chair I and Interdisciplinary Center for, Molecular Materials (ICMM), Friedrich-Alexander University of, Erlangen-Nürnberg, Nikolaus Fiebiger-Straße 10, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0003-4845-0951
Friedrich-Alexander-Universität Erlangen-Nürnberg · DECzech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZGerman Centre for Cardiovascular Research · DEUniversity of Göttingen · DE

Funding

Alexander von Humboldt-StiftungDeutsche Forschungsgemeinschaft Gottfried Wilhelm Leibniz awardDeutsche Forschungsgemeinschaft GRK 2504 (A1/MM)Deutsche Forschungsgemeinschaft MM 1289/11-1Deutsche Forschungsgemeinschaft MM 1289/7-1/7-3Deutsche Forschungsgemeinschaft TS 87/16-3Deutscher Akademischer AustauschdienstERDF/ESF ChemBioDrug CZ.02.1.01/0.0/0.0/16_019/0000729
6 · The paper itself

Abstract

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

Indexed as

VirusesAntiviral AgentsArtemisininsClick ChemistryCytomegalovirusHumansQuinolinesAntiviral AgentsArtemisininsQuinolinesantiviral agentsartemisininsclick chemistrycycloadditionquinolines

Identifiers

PMID32485071
PMCPMC7540715
OpenAlexW3072231594

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.