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/Curation ); précédent : 000207; suivant : 000209Design 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 WuSource :
- MedChemComm [ 2040-2503 ] ; 2018.
Abstract
Url:
DOI: 10.1039/c8md00474a
PubMed: 31559005
PubMed Central: 6735340
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PMC:6735340Le document en format XML
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<fn id="fn1"><p>†Electronic supplementary information (ESI) available: NMR spectra of <bold>11–12</bold>
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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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