N′-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies
Identifieur interne : 001699 ( Ncbi/Curation ); précédent : 001698; suivant : 001700N′-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies
Auteurs : Pradeep Kumar [Inde] ; Balasubramanian Narasimhan [Inde] ; Kalavathy Ramasamy ; Vasudevan Mani ; Rakesh Kumar Mishra ; Abu Bakar Abdul Majeed ; Erik De Clercq [Belgique]Source :
- Monatshefte Fur Chemie [ 0026-9247 ] ; 2012.
Abstract
A variety of
Url:
DOI: 10.1007/s00706-012-0877-3
PubMed: NONE
PubMed Central: 7087754
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Kalavathy Ramasamy<affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="GRID">grid.412259.9</institution-id>
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<institution>Universiti Teknologi MARA (UiTM),</institution>
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Bandar Puncak Alam, 42300 Shan Alam, Selangor Malaysia</nlm:aff>
<wicri:noCountry code="subfield">Selangor Malaysia</wicri:noCountry>
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Bandar Puncak Alam, 42300 Shan Alam, Selangor Malaysia</nlm:aff>
<wicri:noCountry code="subfield">Selangor Malaysia</wicri:noCountry>
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Le document en format XML
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′-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies</title>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main"><italic>N</italic>
′-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies</title>
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Rohtak, 124001 India</nlm:aff>
<country xml:lang="fr">Inde</country>
<wicri:regionArea>Rohtak</wicri:regionArea>
</affiliation>
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<author><name sortKey="Narasimhan, Balasubramanian" sort="Narasimhan, Balasubramanian" uniqKey="Narasimhan B" first="Balasubramanian" last="Narasimhan">Balasubramanian Narasimhan</name>
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Rohtak, 124001 India</nlm:aff>
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<author><name sortKey="Ramasamy, Kalavathy" sort="Ramasamy, Kalavathy" uniqKey="Ramasamy K" first="Kalavathy" last="Ramasamy">Kalavathy Ramasamy</name>
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Bandar Puncak Alam, 42300 Shan Alam, Selangor Malaysia</nlm:aff>
<wicri:noCountry code="subfield">Selangor Malaysia</wicri:noCountry>
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<author><name sortKey="Mani, Vasudevan" sort="Mani, Vasudevan" uniqKey="Mani V" first="Vasudevan" last="Mani">Vasudevan Mani</name>
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<wicri:noCountry code="subfield">Selangor Malaysia</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Mishra, Rakesh Kumar" sort="Mishra, Rakesh Kumar" uniqKey="Mishra R" first="Rakesh Kumar" last="Mishra">Rakesh Kumar Mishra</name>
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<author><name sortKey="Majeed, Abu Bakar Abdul" sort="Majeed, Abu Bakar Abdul" uniqKey="Majeed A" first="Abu Bakar Abdul" last="Majeed">Abu Bakar Abdul Majeed</name>
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Minderbroedersstraat 10, 3000 Louvain, Belgium</nlm:aff>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Minderbroedersstraat 10, 3000 Louvain</wicri:regionArea>
<placeName><region type="province" nuts="2">Province du Brabant flamand</region>
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<series><title level="j">Monatshefte Fur Chemie</title>
<idno type="ISSN">0026-9247</idno>
<idno type="eISSN">1434-4475</idno>
<imprint><date when="2012">2012</date>
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<front><div type="abstract" xml:lang="en"><sec><title>Abstract</title>
<p>A variety of <italic>N</italic>
′-[4-[(substituted imino)methyl]benzylidene]-substituted benzohydrazides have been synthesized and evaluated for antimicrobial and anticancer potential. Results from testing of antimicrobial activity indicated the most potent antimicrobial agents had p<italic>MIC</italic>
<sub>am</sub>
= 1.51. The synthesized compounds were bacteriostatic and fungistatic in action. Results from evaluation of antiviral activity indicated that none of the synthesized hydrazide derivatives inhibited viral replication at sub-toxic concentrations. Results from anti-HIV screening against HIV-2 strain ROD indicated that one compound was more potent (<italic>IC</italic>
<sub>50</sub>
≥ 1 μg/cm<sup>3</sup>
) than the standard drug nevirapine (<italic>IC</italic>
<sub>50</sub>
≥ 4 μg/cm<sup>3</sup>
) and another was equipotent (<italic>IC</italic>
<sub>50</sub>
≥ 4 μg/cm<sup>3</sup>
). The most effective anticancer agent against both HCT116 and MCF7 cancer cell lines had <italic>IC</italic>
<sub>50</sub>
= 19 and 18 μg/cm<sup>3</sup>
, respectively. QSAR analysis indicated the importance of Wiener index (<italic>W</italic>
) and energy of the lowest unoccupied molecular orbital (LUMO) in describing the antimicrobial activity of the synthesized compounds.</p>
</sec>
<sec><title>Graphical Abstract</title>
<p><graphic position="anchor" xlink:href="706_2012_877_Figa_HTML" id="MO1"></graphic>
</p>
</sec>
</div>
</front>
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