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In Vitro Antiviral Activity of some Novel Isatin Derivatives against HCV and SARS-CoV Viruses

Identifieur interne : 000170 ( Ncbi/Merge ); précédent : 000169; suivant : 000171

In Vitro Antiviral Activity of some Novel Isatin Derivatives against HCV and SARS-CoV Viruses

Auteurs : P. Selvam [Inde] ; N. Murgesh [Inde] ; M. Chandramohan [Belgique] ; E. De Clercq [Belgique] ; E. Keyaerts [Belgique] ; L. Vijgen [Belgique] ; P. Maes [Belgique] ; J. Neyts [Belgique] ; M. V. Ranst [Belgique]

Source :

RBID : PMC:2852069

Abstract

4-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)amino]-N(4,6-dimethyl-2-pyrimidiny)benzene sulphonamide and its derivatives were evaluated for antiviral activity against Pathogenic viruses such as Hepatitis C Virus and SARS-CoV in Vero and Huh 5-2 cells, respectively. The 5-fluoro derivative inhibited the HCV RNA synthesis at 6 μg/ml, without toxicity at a concentration up to 42 μg/ml in Huh 5-2 cells. Among the compounds tested SPIII-5F exhibits the 45% maximum protection against replication of SARS-CoV in Vero cells.


Url:
DOI: 10.4103/0250-474X.40339
PubMed: 20390088
PubMed Central: 2852069

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PMC:2852069

Le document en format XML

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<p>4-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)amino]-N(4,6-dimethyl-2-pyrimidiny)benzene sulphonamide and its derivatives were evaluated for antiviral activity against Pathogenic viruses such as Hepatitis C Virus and SARS-CoV in Vero and Huh 5-2 cells, respectively. The 5-fluoro derivative inhibited the HCV RNA synthesis at 6 μg/ml, without toxicity at a concentration up to 42 μg/ml in Huh 5-2 cells. Among the compounds tested SPIII-5F exhibits the 45% maximum protection against replication of SARS-CoV in Vero cells.</p>
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<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Indian J Pharm Sci</journal-id>
<journal-id journal-id-type="publisher-id">IJPhS</journal-id>
<journal-title-group>
<journal-title>Indian Journal of Pharmaceutical Sciences</journal-title>
</journal-title-group>
<issn pub-type="ppub">0250-474X</issn>
<issn pub-type="epub">1998-3743</issn>
<publisher>
<publisher-name>Medknow Publications</publisher-name>
<publisher-loc>India</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">20390088</article-id>
<article-id pub-id-type="pmc">2852069</article-id>
<article-id pub-id-type="publisher-id">IJPhS-70-91</article-id>
<article-id pub-id-type="doi">10.4103/0250-474X.40339</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Short Communication</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>
<italic>In Vitro</italic>
Antiviral Activity of some Novel Isatin Derivatives against HCV and SARS-CoV Viruses</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Selvam</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="AF0001"></xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Murgesh</surname>
<given-names>N.</given-names>
</name>
<xref ref-type="aff" rid="AF0002">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chandramohan</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="AF0003">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Clercq</surname>
<given-names>E.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Keyaerts</surname>
<given-names>E.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Vijgen</surname>
<given-names>L.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Maes</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Neyts</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ranst</surname>
<given-names>M. V.</given-names>
</name>
<xref ref-type="aff" rid="AF0004">3</xref>
</contrib>
</contrib-group>
<aff id="AF0001">Arulmigu Kalasalingam College of Pharmacy, Krishnankoil - 626 190, India</aff>
<aff id="AF0002">
<label>1</label>
Institute of Pharmacology, Madurai Medical College, Madurai - 625 020, India</aff>
<aff id="AF0003">
<label>2</label>
Bharat Ratna Kamarajar Liver Hospital and Research Center, Madurai - 625 001, Belgium</aff>
<aff id="AF0004">
<label>3</label>
Raga Institute for Medical Research, Katholieke Universiteit-Leuven, Minder broederstraat 10, LeuvenB-3000, Belgium</aff>
<author-notes>
<corresp id="cor1">
<label>*</label>
<bold>For correspondence</bold>
E-mail:
<email xlink:href="periyasamyselvam2001@yahoo.co.in">periyasamyselvam2001@yahoo.co.in</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<season>Jan-Feb</season>
<year>2008</year>
</pub-date>
<volume>70</volume>
<issue>1</issue>
<fpage>91</fpage>
<lpage>94</lpage>
<history>
<date date-type="received">
<day>06</day>
<month>7</month>
<year>2006</year>
</date>
<date date-type="rev-recd">
<day>23</day>
<month>7</month>
<year>2007</year>
</date>
<date date-type="accepted">
<day>29</day>
<month>1</month>
<year>2008</year>
</date>
</history>
<permissions>
<copyright-statement>© Indian Journal of Pharmaceutical Sciences</copyright-statement>
<copyright-year>2008</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>4-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)amino]-N(4,6-dimethyl-2-pyrimidiny)benzene sulphonamide and its derivatives were evaluated for antiviral activity against Pathogenic viruses such as Hepatitis C Virus and SARS-CoV in Vero and Huh 5-2 cells, respectively. The 5-fluoro derivative inhibited the HCV RNA synthesis at 6 μg/ml, without toxicity at a concentration up to 42 μg/ml in Huh 5-2 cells. Among the compounds tested SPIII-5F exhibits the 45% maximum protection against replication of SARS-CoV in Vero cells.</p>
</abstract>
<kwd-group>
<kwd>Isatin</kwd>
<kwd>HCV</kwd>
<kwd>SARS-CoV</kwd>
<kwd>vero cells</kwd>
<kwd>huh 5-2 cells</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Belgique</li>
<li>Inde</li>
</country>
<region>
<li>Province du Brabant flamand</li>
<li>Région flamande</li>
</region>
<settlement>
<li>Louvain</li>
</settlement>
<orgName>
<li>Katholieke Universiteit Leuven</li>
</orgName>
</list>
<tree>
<country name="Inde">
<noRegion>
<name sortKey="Selvam, P" sort="Selvam, P" uniqKey="Selvam P" first="P." last="Selvam">P. Selvam</name>
</noRegion>
<name sortKey="Murgesh, N" sort="Murgesh, N" uniqKey="Murgesh N" first="N." last="Murgesh">N. Murgesh</name>
</country>
<country name="Belgique">
<noRegion>
<name sortKey="Chandramohan, M" sort="Chandramohan, M" uniqKey="Chandramohan M" first="M." last="Chandramohan">M. Chandramohan</name>
</noRegion>
<name sortKey="De Clercq, E" sort="De Clercq, E" uniqKey="De Clercq E" first="E." last="De Clercq">E. De Clercq</name>
<name sortKey="Keyaerts, E" sort="Keyaerts, E" uniqKey="Keyaerts E" first="E." last="Keyaerts">E. Keyaerts</name>
<name sortKey="Maes, P" sort="Maes, P" uniqKey="Maes P" first="P." last="Maes">P. Maes</name>
<name sortKey="Neyts, J" sort="Neyts, J" uniqKey="Neyts J" first="J." last="Neyts">J. Neyts</name>
<name sortKey="Ranst, M V" sort="Ranst, M V" uniqKey="Ranst M" first="M. V." last="Ranst">M. V. Ranst</name>
<name sortKey="Vijgen, L" sort="Vijgen, L" uniqKey="Vijgen L" first="L." last="Vijgen">L. Vijgen</name>
</country>
</tree>
</affiliations>
</record>

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