Inhibition of SARS coronavirus helicase by bismuth complexes.
Identifieur interne : 001A97 ( Ncbi/Curation ); précédent : 001A96; suivant : 001A98Inhibition of SARS coronavirus helicase by bismuth complexes.
Auteurs : Nan Yang [République populaire de Chine] ; Julian A. Tanner ; Zai Wang ; Jian-Dong Huang ; Bo-Jian Zheng ; Nianyong Zhu ; Hongzhe SunSource :
- Chemical communications (Cambridge, England) [ 1359-7345 ] ; 2007.
Descripteurs français
- KwdFr :
- Adenosine triphosphatases (antagonistes et inhibiteurs), Antienzymes (pharmacologie), Antienzymes (synthèse chimique), Antiviraux (pharmacologie), Antiviraux (synthèse chimique), Bismuth (), Chromatographie en phase liquide à haute performance, Composés organométalliques (pharmacologie), Composés organométalliques (synthèse chimique), Cristallographie aux rayons X, Diméthylsulfoxyde, Helicase (antagonistes et inhibiteurs), Modèles moléculaires, Porphyrines (pharmacologie), Porphyrines (synthèse chimique), Virus du SRAS (enzymologie), Zinc ().
- MESH :
- antagonistes et inhibiteurs : Adenosine triphosphatases, Helicase.
- enzymologie : Virus du SRAS.
- pharmacologie : Antienzymes, Antiviraux, Composés organométalliques, Porphyrines.
- synthèse chimique : Antienzymes, Antiviraux, Composés organométalliques, Porphyrines.
- Bismuth, Chromatographie en phase liquide à haute performance, Cristallographie aux rayons X, Diméthylsulfoxyde, Modèles moléculaires, Zinc.
English descriptors
- KwdEn :
- Adenosine Triphosphatases (antagonists & inhibitors), Antiviral Agents (chemical synthesis), Antiviral Agents (pharmacology), Bismuth (chemistry), Chromatography, High Pressure Liquid, Crystallography, X-Ray, DNA Helicases (antagonists & inhibitors), Dimethyl Sulfoxide, Enzyme Inhibitors (chemical synthesis), Enzyme Inhibitors (pharmacology), Models, Molecular, Organometallic Compounds (chemical synthesis), Organometallic Compounds (pharmacology), Porphyrins (chemical synthesis), Porphyrins (pharmacology), SARS Virus (enzymology), Zinc (chemistry).
- MESH :
- chemical , antagonists & inhibitors : Adenosine Triphosphatases, DNA Helicases.
- chemical , chemical synthesis : Antiviral Agents, Enzyme Inhibitors, Organometallic Compounds, Porphyrins.
- chemical , chemistry : Bismuth, Zinc.
- chemical , pharmacology : Antiviral Agents, Enzyme Inhibitors, Organometallic Compounds, Porphyrins.
- enzymology : SARS Virus.
- Chromatography, High Pressure Liquid, Crystallography, X-Ray, Dimethyl Sulfoxide, Models, Molecular.
Abstract
A series of bismuth complexes were synthesized and characterized, and most of them exhibited inhibition against the SARS coronavirus helicase ATPase and duplex-unwinding activities at micromolar concentrations.
DOI: 10.1039/b709515e
PubMed: 17957304
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pubmed:17957304Le document en format XML
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<author><name sortKey="Yang, Nan" sort="Yang, Nan" uniqKey="Yang N" first="Nan" last="Yang">Nan Yang</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, PR China.</nlm:affiliation>
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<term>Bismuth (chemistry)</term>
<term>Chromatography, High Pressure Liquid</term>
<term>Crystallography, X-Ray</term>
<term>DNA Helicases (antagonists & inhibitors)</term>
<term>Dimethyl Sulfoxide</term>
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<term>Antiviraux (pharmacologie)</term>
<term>Antiviraux (synthèse chimique)</term>
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<term>Helicase (antagonistes et inhibiteurs)</term>
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<term>Porphyrines (pharmacologie)</term>
<term>Porphyrines (synthèse chimique)</term>
<term>Virus du SRAS (enzymologie)</term>
<term>Zinc ()</term>
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<term>DNA Helicases</term>
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<term>Organometallic Compounds</term>
<term>Porphyrins</term>
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<term>Enzyme Inhibitors</term>
<term>Organometallic Compounds</term>
<term>Porphyrins</term>
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<term>Composés organométalliques</term>
<term>Porphyrines</term>
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<term>Composés organométalliques</term>
<term>Porphyrines</term>
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<term>Crystallography, X-Ray</term>
<term>Dimethyl Sulfoxide</term>
<term>Models, Molecular</term>
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<term>Chromatographie en phase liquide à haute performance</term>
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<front><div type="abstract" xml:lang="en">A series of bismuth complexes were synthesized and characterized, and most of them exhibited inhibition against the SARS coronavirus helicase ATPase and duplex-unwinding activities at micromolar concentrations.</div>
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