CovidV2, PascalFrancis, Checkpoint, bibRecord, 000014

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones

Identifieur interne : 000014 ( PascalFrancis/Checkpoint ); précédent : 000013; suivant : 000015

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones

Auteurs : KRISHNAN SURESH KUMAR [Inde] ; Swastika Ganguly [Inde] ; Ravichandran Veerasamy [Malaisie] ; Erik De Clercq [Belgique]

Source :

European journal of medicinal chemistry [ 0223-5234 ] ; 2010.

RBID : Pascal:11-0128463

Descripteurs français

Pascal (Inist)
- Synthèse chimique, Antiviral, Relation structure activité, Composé non nucléoside, Hétérocycle azote, Virus péritonite infectieuse féline, Herpesvirus hominis, Composé bicyclique, Virus vaccine, Virus stomatite vésiculeuse, Composé aromatique, Dérivé du benzène, In vitro, Dérivé de la quinazoline, Quinazolin-4-one dérivé.

English descriptors

KwdEn :
- Antiviral, Aromatic compound, Benzene derivatives, Bicyclic compound, Chemical synthesis, Feline infectious peritonitis virus, Herpesvirus hominis, In vitro, Nitrogen heterocycle, Non nucleoside compound, Quinazoline derivatives, Structure activity relation, Vaccinia virus, Vesicular stomatitis virus.

Abstract

A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral studies. Cytotoxicity and antiviral activity were evaluated against herpes simplex virus-1 (KOS), herpes simplex virus-2 (G), vaccinia virus, vesicular stomatitis virus, herpes simplex virus-1 TK- KOS ACVr, para influenza-3 virus, reovirus-1, Sindbis virus, Coxsackie virus B4, Punta Toro virus, feline corona virus (FIPV), feline herpes virus, respiratory syncytial virus, influenza A H1N1 subtype, influenza A H3N2 subtype, and influenza B virus. Compound 2a showed better antiviral activity against the entire tested virus.

Affiliations:

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

to stream PascalFrancis, to step Corpus: 000015
to stream PascalFrancis, to step Curation: 000044

Links to Exploration step

Pascal:11-0128463

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones</title>
<author><name sortKey="Krishnan Suresh Kumar" sort="Krishnan Suresh Kumar" uniqKey="Krishnan Suresh Kumar" last="Krishnan Suresh Kumar">KRISHNAN SURESH KUMAR</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Medicinal chemistry research Laboratory, KMCH College of Pharmacy</s1>
<s2>Coimbatore</s2>
<s3>IND</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Coimbatore</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ganguly, Swastika" sort="Ganguly, Swastika" uniqKey="Ganguly S" first="Swastika" last="Ganguly">Swastika Ganguly</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Medicinal chemistry research Laboratory, Department of Pharmaceutical Sciences, Birla Institute of Technology</s1>
<s2>Ranchi</s2>
<s3>IND</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Ranchi</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Veerasamy, Ravichandran" sort="Veerasamy, Ravichandran" uniqKey="Veerasamy R" first="Ravichandran" last="Veerasamy">Ravichandran Veerasamy</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Faculty of Pharmacy, AIMST University</s1>
<s3>MYS</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Malaisie</country>
<wicri:noRegion>Faculty of Pharmacy, AIMST University</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="De Clercq, Erik" sort="De Clercq, Erik" uniqKey="De Clercq E" first="Erik" last="De Clercq">Erik De Clercq</name>
<affiliation wicri:level="4"><inist:fA14 i1="04"><s1>Rega Institute for Medical research, Katholieke Universiteit Leuven</s1>
<s2>3000 Leuven</s2>
<s3>BEL</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName><region type="province" nuts="2">Province du Brabant flamand</region>
<settlement type="city">Louvain</settlement>
</placeName>
<orgName type="university">Katholieke Universiteit Leuven</orgName>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">11-0128463</idno>
<date when="2010">2010</date>
<idno type="stanalyst">PASCAL 11-0128463 INIST</idno>
<idno type="RBID">Pascal:11-0128463</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000015</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000044</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000014</idno>
<idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">000014</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones</title>
<author><name sortKey="Krishnan Suresh Kumar" sort="Krishnan Suresh Kumar" uniqKey="Krishnan Suresh Kumar" last="Krishnan Suresh Kumar">KRISHNAN SURESH KUMAR</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Medicinal chemistry research Laboratory, KMCH College of Pharmacy</s1>
<s2>Coimbatore</s2>
<s3>IND</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Coimbatore</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ganguly, Swastika" sort="Ganguly, Swastika" uniqKey="Ganguly S" first="Swastika" last="Ganguly">Swastika Ganguly</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Medicinal chemistry research Laboratory, Department of Pharmaceutical Sciences, Birla Institute of Technology</s1>
<s2>Ranchi</s2>
<s3>IND</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Ranchi</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Veerasamy, Ravichandran" sort="Veerasamy, Ravichandran" uniqKey="Veerasamy R" first="Ravichandran" last="Veerasamy">Ravichandran Veerasamy</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Faculty of Pharmacy, AIMST University</s1>
<s3>MYS</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Malaisie</country>
<wicri:noRegion>Faculty of Pharmacy, AIMST University</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="De Clercq, Erik" sort="De Clercq, Erik" uniqKey="De Clercq E" first="Erik" last="De Clercq">Erik De Clercq</name>
<affiliation wicri:level="4"><inist:fA14 i1="04"><s1>Rega Institute for Medical research, Katholieke Universiteit Leuven</s1>
<s2>3000 Leuven</s2>
<s3>BEL</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName><region type="province" nuts="2">Province du Brabant flamand</region>
<settlement type="city">Louvain</settlement>
</placeName>
<orgName type="university">Katholieke Universiteit Leuven</orgName>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">European journal of medicinal chemistry</title>
<title level="j" type="abbreviated">Eur. j. med. chem.</title>
<idno type="ISSN">0223-5234</idno>
<imprint><date when="2010">2010</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">European journal of medicinal chemistry</title>
<title level="j" type="abbreviated">Eur. j. med. chem.</title>
<idno type="ISSN">0223-5234</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antiviral</term>
<term>Aromatic compound</term>
<term>Benzene derivatives</term>
<term>Bicyclic compound</term>
<term>Chemical synthesis</term>
<term>Feline infectious peritonitis virus</term>
<term>Herpesvirus hominis</term>
<term>In vitro</term>
<term>Nitrogen heterocycle</term>
<term>Non nucleoside compound</term>
<term>Quinazoline derivatives</term>
<term>Structure activity relation</term>
<term>Vaccinia virus</term>
<term>Vesicular stomatitis virus</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Synthèse chimique</term>
<term>Antiviral</term>
<term>Relation structure activité</term>
<term>Composé non nucléoside</term>
<term>Hétérocycle azote</term>
<term>Virus péritonite infectieuse féline</term>
<term>Herpesvirus hominis</term>
<term>Composé bicyclique</term>
<term>Virus vaccine</term>
<term>Virus stomatite vésiculeuse</term>
<term>Composé aromatique</term>
<term>Dérivé du benzène</term>
<term>In vitro</term>
<term>Dérivé de la quinazoline</term>
<term>Quinazolin-4-one dérivé</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral studies. Cytotoxicity and antiviral activity were evaluated against herpes simplex virus-1 (KOS), herpes simplex virus-2 (G), vaccinia virus, vesicular stomatitis virus, herpes simplex virus-1 TK- KOS ACVr, para influenza-3 virus, reovirus-1, Sindbis virus, Coxsackie virus B4, Punta Toro virus, feline corona virus (FIPV), feline herpes virus, respiratory syncytial virus, influenza A H1N1 subtype, influenza A H3N2 subtype, and influenza B virus. Compound 2a showed better antiviral activity against the entire tested virus.</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0223-5234</s0>
</fA01>
<fA02 i1="01"><s0>EJMCA5</s0>
</fA02>
<fA03 i2="1"><s0>Eur. j. med. chem.</s0>
</fA03>
<fA05><s2>45</s2>
</fA05>
<fA06><s2>11</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>KRISHNAN SURESH KUMAR</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>GANGULY (Swastika)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>VEERASAMY (Ravichandran)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>DE CLERCQ (Erik)</s1>
</fA11>
<fA14 i1="01"><s1>Medicinal chemistry research Laboratory, KMCH College of Pharmacy</s1>
<s2>Coimbatore</s2>
<s3>IND</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Medicinal chemistry research Laboratory, Department of Pharmaceutical Sciences, Birla Institute of Technology</s1>
<s2>Ranchi</s2>
<s3>IND</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Faculty of Pharmacy, AIMST University</s1>
<s3>MYS</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Rega Institute for Medical research, Katholieke Universiteit Leuven</s1>
<s2>3000 Leuven</s2>
<s3>BEL</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA20><s1>5474-5479</s1>
</fA20>
<fA21><s1>2010</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>12640</s2>
<s5>354000193329240940</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2011 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>20 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>11-0128463</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>European journal of medicinal chemistry</s0>
</fA64>
<fA66 i1="01"><s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral studies. Cytotoxicity and antiviral activity were evaluated against herpes simplex virus-1 (KOS), herpes simplex virus-2 (G), vaccinia virus, vesicular stomatitis virus, herpes simplex virus-1 TK- KOS ACVr, para influenza-3 virus, reovirus-1, Sindbis virus, Coxsackie virus B4, Punta Toro virus, feline corona virus (FIPV), feline herpes virus, respiratory syncytial virus, influenza A H1N1 subtype, influenza A H3N2 subtype, and influenza B virus. Compound 2a showed better antiviral activity against the entire tested virus.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B02S05</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Synthèse chimique</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Chemical synthesis</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Síntesis química</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Antiviral</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Antiviral</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Antiviral</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Relation structure activité</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Structure activity relation</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Relación estructura actividad</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Composé non nucléoside</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Non nucleoside compound</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Compuesto no nucleósido</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Hétérocycle azote</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Nitrogen heterocycle</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Heterociclo nitrógeno</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Virus péritonite infectieuse féline</s0>
<s2>NW</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Feline infectious peritonitis virus</s0>
<s2>NW</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Feline infectious peritonitis virus</s0>
<s2>NW</s2>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Herpesvirus hominis</s0>
<s2>NW</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Herpesvirus hominis</s0>
<s2>NW</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Herpesvirus hominis</s0>
<s2>NW</s2>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Composé bicyclique</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Bicyclic compound</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Compuesto bicíclico</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Virus vaccine</s0>
<s2>NW</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Vaccinia virus</s0>
<s2>NW</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Vaccinia virus</s0>
<s2>NW</s2>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Virus stomatite vésiculeuse</s0>
<s2>NW</s2>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Vesicular stomatitis virus</s0>
<s2>NW</s2>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Vesicular stomatitis virus</s0>
<s2>NW</s2>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Composé aromatique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Aromatic compound</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Compuesto aromático</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Dérivé du benzène</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Benzene derivatives</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Benceno derivado</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE"><s0>Dérivé de la quinazoline</s0>
<s2>FR</s2>
<s5>33</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG"><s0>Quinazoline derivatives</s0>
<s2>FR</s2>
<s5>33</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Quinazolin-4-one dérivé</s0>
<s2>NK</s2>
<s4>INC</s4>
<s5>76</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Alphaherpesvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Alphaherpesvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Alphaherpesvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Herpesviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Herpesviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Herpesviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Orthopoxvirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Orthopoxvirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Orthopoxvirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Chordopoxvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Chordopoxvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Chordopoxvirinae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Poxviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Poxviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Poxviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Vesiculovirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Vesiculovirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Vesiculovirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Rhabdoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Rhabdoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Rhabdoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="12" i2="X" l="FRE"><s0>Mononegavirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="12" i2="X" l="ENG"><s0>Mononegavirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="12" i2="X" l="SPA"><s0>Mononegavirales</s0>
<s2>NW</s2>
</fC07>
<fN21><s1>087</s1>
</fN21>
</pA>
</standard>
</inist>
<affiliations><list><country><li>Belgique</li>
<li>Inde</li>
<li>Malaisie</li>
</country>
<region><li>Province du Brabant flamand</li>
</region>
<settlement><li>Louvain</li>
</settlement>
<orgName><li>Katholieke Universiteit Leuven</li>
</orgName>
</list>
<tree><country name="Inde"><noRegion><name sortKey="Krishnan Suresh Kumar" sort="Krishnan Suresh Kumar" uniqKey="Krishnan Suresh Kumar" last="Krishnan Suresh Kumar">KRISHNAN SURESH KUMAR</name>
</noRegion>
<name sortKey="Ganguly, Swastika" sort="Ganguly, Swastika" uniqKey="Ganguly S" first="Swastika" last="Ganguly">Swastika Ganguly</name>
</country>
<country name="Malaisie"><noRegion><name sortKey="Veerasamy, Ravichandran" sort="Veerasamy, Ravichandran" uniqKey="Veerasamy R" first="Ravichandran" last="Veerasamy">Ravichandran Veerasamy</name>
</noRegion>
</country>
<country name="Belgique"><region name="Province du Brabant flamand"><name sortKey="De Clercq, Erik" sort="De Clercq, Erik" uniqKey="De Clercq E" first="Erik" last="De Clercq">Erik De Clercq</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/CovidV2/Data/PascalFrancis/Checkpoint

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000014 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Checkpoint/biblio.hfd -nk 000014 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    CovidV2
   |flux=    PascalFrancis
   |étape=   Checkpoint
   |type=    RBID
   |clé=     Pascal:11-0128463
   |texte=   Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones
}}

This area was generated with Dilib version V0.6.33.
Data generation: Sat Mar 28 17:51:24 2020. Site generation: Sun Jan 31 15:35:48 2021

	Serveur d'exploration Covid (26 mars)
	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.

Serveur d'exploration Covid (26 mars)

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones

Source :

Descripteurs français

English descriptors

Abstract

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

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri