H2N2V1, Main, Exploration, bibRecord, 000208

Design and synthesis of heteroaromatic-based benzenesulfonamide derivatives as potent inhibitors of H5N1 influenza A virus††Electronic supplementary information (ESI) available: NMR spectra of 11–12. See DOI: 10.1039/c8md00474a

Identifieur interne : 000208 ( Main/Exploration ); précédent : 000207; suivant : 000209

Design and synthesis of heteroaromatic-based benzenesulfonamide derivatives as potent inhibitors of H5N1 influenza A virus††Electronic supplementary information (ESI) available: NMR spectra of 11–12. See DOI: 10.1039/c8md00474a

Auteurs : Yongshi Yu ; Zhichao Xu ; Liaoqi Du ; Mengyu Jin ; Chune Dong ; Hai-Bing Zhou ; Shuwen Wu

Source :

MedChemComm [ 2040-2503 ] ; 2018.

RBID : PMC:6735340

Abstract

A novel series of heteroaromatic-based benzenesulfonamide derivatives were identified as potent inhibitors of H5N1 influenza A virus.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735340

DOI: 10.1039/c8md00474a
PubMed: 31559005
PubMed Central: 6735340

Affiliations:

Le document en format XML

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<fn id="fn1"><p>†Electronic supplementary information (ESI) available: NMR spectra of <bold>11–12</bold>
. See DOI: <uri xlink:type="simple" xlink:href="https://doi.org/10.1039/c8md00474a">10.1039/c8md00474a</uri>
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<author><name sortKey="Yu, Yongshi" sort="Yu, Yongshi" uniqKey="Yu Y" first="Yongshi" last="Yu">Yongshi Yu</name>
<affiliation><nlm:aff id="affa"> State Key Laboratory of Virology , College of Life Sciences , Wuhan University , Wuhan 430072 , China . Email:<email>shuwenwu@hotmail.com</email>
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<affiliation><nlm:aff id="affb"> Hubei Province Key Laboratory of Allergy and Immunology , Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals , Wuhan University School of Pharmaceutical Sciences , Wuhan 430071 , China . Email:<email>zhouhb@whu.edu.cn</email>
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<front><div type="abstract" xml:lang="en"><p><graphic xlink:href="c8md00474a-ga.jpg" id="ga" position="float" orientation="portrait"></graphic>
A novel series of heteroaromatic-based benzenesulfonamide derivatives were identified as potent inhibitors of H5N1 influenza A virus.</p>
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<name sortKey="Du, Liaoqi" sort="Du, Liaoqi" uniqKey="Du L" first="Liaoqi" last="Du">Liaoqi Du</name>
<name sortKey="Jin, Mengyu" sort="Jin, Mengyu" uniqKey="Jin M" first="Mengyu" last="Jin">Mengyu Jin</name>
<name sortKey="Wu, Shuwen" sort="Wu, Shuwen" uniqKey="Wu S" first="Shuwen" last="Wu">Shuwen Wu</name>
<name sortKey="Xu, Zhichao" sort="Xu, Zhichao" uniqKey="Xu Z" first="Zhichao" last="Xu">Zhichao Xu</name>
<name sortKey="Yu, Yongshi" sort="Yu, Yongshi" uniqKey="Yu Y" first="Yongshi" last="Yu">Yongshi Yu</name>
<name sortKey="Zhou, Hai Bing" sort="Zhou, Hai Bing" uniqKey="Zhou H" first="Hai-Bing" last="Zhou">Hai-Bing Zhou</name>
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Serveur d'exploration H2N2

Design and synthesis of heteroaromatic-based benzenesulfonamide derivatives as potent inhibitors of H5N1 influenza A virus††Electronic supplementary information (ESI) available: NMR spectra of 11–12. See DOI: 10.1039/c8md00474a

Design and synthesis of heteroaromatic-based benzenesulfonamide derivatives as potent inhibitors of H5N1 influenza A virus††Electronic supplementary information (ESI) available: NMR spectra of 11–12. See DOI: 10.1039/c8md00474a

Source :

Abstract

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