Serveur d'exploration SRAS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Helicases as antiviral drug targets.

Identifieur interne : 003104 ( Main/Exploration ); précédent : 003103; suivant : 003105

Helicases as antiviral drug targets.

Auteurs : J D Huang [Hong Kong] ; B J Zheng ; H Z Sun

Source :

RBID : pubmed:18708673

Descripteurs français

English descriptors

Abstract

1. We have demonstrated for the first time that the helicase of a ribonucleic acid virus, the SARS coronavirus (SARS-CoV), is a valid target for drug development. 2. Using high throughput screen and chemical synthesis, several lead compounds targeting the SARS-CoV helicase have been identified. We have shown that these compounds can inhibit SARS-CoV helicase activity and viral growth in cell culture systems. These compounds can potentially be used to target other viruses.

PubMed: 18708673


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Helicases as antiviral drug targets.</title>
<author>
<name sortKey="Huang, J D" sort="Huang, J D" uniqKey="Huang J" first="J D" last="Huang">J D Huang</name>
<affiliation wicri:level="1">
<nlm:affiliation>Department of Biochemistry, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong. jdhuang@hkucc.hku.hk</nlm:affiliation>
<country xml:lang="fr">Hong Kong</country>
<wicri:regionArea>Department of Biochemistry, The University of Hong Kong, 21 Sassoon Road, Pokfulam</wicri:regionArea>
<wicri:noRegion>Pokfulam</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Zheng, B J" sort="Zheng, B J" uniqKey="Zheng B" first="B J" last="Zheng">B J Zheng</name>
</author>
<author>
<name sortKey="Sun, H Z" sort="Sun, H Z" uniqKey="Sun H" first="H Z" last="Sun">H Z Sun</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2008">2008</date>
<idno type="RBID">pubmed:18708673</idno>
<idno type="pmid">18708673</idno>
<idno type="wicri:Area/PubMed/Corpus">001999</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001999</idno>
<idno type="wicri:Area/PubMed/Curation">001999</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001999</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001B24</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">001B24</idno>
<idno type="wicri:Area/Ncbi/Merge">001D27</idno>
<idno type="wicri:Area/Ncbi/Curation">001D27</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">001D27</idno>
<idno type="wicri:doubleKey">1024-2708:2008:Huang J:helicases:as:antiviral</idno>
<idno type="wicri:Area/Main/Merge">003190</idno>
<idno type="wicri:Area/Main/Curation">003104</idno>
<idno type="wicri:Area/Main/Exploration">003104</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Helicases as antiviral drug targets.</title>
<author>
<name sortKey="Huang, J D" sort="Huang, J D" uniqKey="Huang J" first="J D" last="Huang">J D Huang</name>
<affiliation wicri:level="1">
<nlm:affiliation>Department of Biochemistry, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong. jdhuang@hkucc.hku.hk</nlm:affiliation>
<country xml:lang="fr">Hong Kong</country>
<wicri:regionArea>Department of Biochemistry, The University of Hong Kong, 21 Sassoon Road, Pokfulam</wicri:regionArea>
<wicri:noRegion>Pokfulam</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Zheng, B J" sort="Zheng, B J" uniqKey="Zheng B" first="B J" last="Zheng">B J Zheng</name>
</author>
<author>
<name sortKey="Sun, H Z" sort="Sun, H Z" uniqKey="Sun H" first="H Z" last="Sun">H Z Sun</name>
</author>
</analytic>
<series>
<title level="j">Hong Kong medical journal = Xianggang yi xue za zhi</title>
<idno type="ISSN">1024-2708</idno>
<imprint>
<date when="2008" type="published">2008</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>Antiviral Agents (pharmacology)</term>
<term>Cells, Cultured</term>
<term>Chlorocebus aethiops</term>
<term>DNA Helicases (genetics)</term>
<term>DNA Helicases (pharmacology)</term>
<term>Drug Delivery Systems</term>
<term>Drug Evaluation, Preclinical</term>
<term>SARS Virus (drug effects)</term>
<term>SARS Virus (genetics)</term>
<term>Sensitivity and Specificity</term>
<term>Severe Acute Respiratory Syndrome (drug therapy)</term>
<term>Severe Acute Respiratory Syndrome (genetics)</term>
<term>Severe Acute Respiratory Syndrome (virology)</term>
<term>Vero Cells (cytology)</term>
<term>Vero Cells (drug effects)</term>
<term>Virus Replication (drug effects)</term>
<term>Virus Replication (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Antiviraux (pharmacologie)</term>
<term>Cellules Vero ()</term>
<term>Cellules Vero (cytologie)</term>
<term>Cellules cultivées</term>
<term>Helicase (génétique)</term>
<term>Helicase (pharmacologie)</term>
<term>Réplication virale ()</term>
<term>Réplication virale (génétique)</term>
<term>Sensibilité et spécificité</term>
<term>Syndrome respiratoire aigu sévère (génétique)</term>
<term>Syndrome respiratoire aigu sévère (traitement médicamenteux)</term>
<term>Syndrome respiratoire aigu sévère (virologie)</term>
<term>Systèmes de délivrance de médicaments</term>
<term>Virus du SRAS ()</term>
<term>Virus du SRAS (génétique)</term>
<term>Évaluation préclinique de médicament</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>DNA Helicases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Antiviral Agents</term>
<term>DNA Helicases</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr">
<term>Cellules Vero</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en">
<term>Vero Cells</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>SARS Virus</term>
<term>Vero Cells</term>
<term>Virus Replication</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>SARS Virus</term>
<term>Severe Acute Respiratory Syndrome</term>
<term>Virus Replication</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Helicase</term>
<term>Réplication virale</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Antiviraux</term>
<term>Helicase</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cells, Cultured</term>
<term>Chlorocebus aethiops</term>
<term>Drug Delivery Systems</term>
<term>Drug Evaluation, Preclinical</term>
<term>Sensitivity and Specificity</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Cellules Vero</term>
<term>Cellules cultivées</term>
<term>Réplication virale</term>
<term>Sensibilité et spécificité</term>
<term>Systèmes de délivrance de médicaments</term>
<term>Virus du SRAS</term>
<term>Évaluation préclinique de médicament</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">1. We have demonstrated for the first time that the helicase of a ribonucleic acid virus, the SARS coronavirus (SARS-CoV), is a valid target for drug development. 2. Using high throughput screen and chemical synthesis, several lead compounds targeting the SARS-CoV helicase have been identified. We have shown that these compounds can inhibit SARS-CoV helicase activity and viral growth in cell culture systems. These compounds can potentially be used to target other viruses.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Hong Kong</li>
</country>
</list>
<tree>
<noCountry>
<name sortKey="Sun, H Z" sort="Sun, H Z" uniqKey="Sun H" first="H Z" last="Sun">H Z Sun</name>
<name sortKey="Zheng, B J" sort="Zheng, B J" uniqKey="Zheng B" first="B J" last="Zheng">B J Zheng</name>
</noCountry>
<country name="Hong Kong">
<noRegion>
<name sortKey="Huang, J D" sort="Huang, J D" uniqKey="Huang J" first="J D" last="Huang">J D Huang</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/SrasV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003104 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003104 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    SrasV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:18708673
   |texte=   Helicases as antiviral drug targets.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:18708673" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a SrasV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 28 14:49:16 2020. Site generation: Sat Mar 27 22:06:49 2021