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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.50B(09) [September 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12640</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12672" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12671" />
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    <title>The Collection's search engine</title>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12674">
    <title>Synthesis and biological evaluation of Mannich bases of benzimidazole derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12674</link>
    <description>Title: Synthesis and biological evaluation of Mannich bases of benzimidazole derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Mariappan, G; Bhuyan, N R; Kumar, Pradeep; Kumar, Deepak; Murali, K
&lt;br/&gt;
&lt;br/&gt;Abstract: [1-(N-substituted amino)&#xD;
methyl]-2-ethyl benzimidazole deri­vatives &lt;b style=""&gt;1-10&lt;/b&gt;&#xD;
have been&lt;b style=""&gt; &lt;/b&gt;synthesized by the&#xD;
condensation of 2-ethyl benzimidazole with substituted primary and secondary&#xD;
amines. Their structures have been elucidated by UV-Vis, IR, &lt;sup&gt;1&lt;/sup&gt;H NMR&#xD;
and mass spectral data. Among the synthesized derivatives &lt;b style=""&gt;1, 2, 8, 9&lt;/b&gt; and &lt;b style=""&gt;10&lt;/b&gt; are&#xD;
found to have an effective anti-inflammatory response whereas compounds &lt;b style=""&gt;2, 4, 6, 8&lt;/b&gt; and &lt;b style=""&gt;10&lt;/b&gt; have potent analgesic response. There is no significant difference in bioactivity of benzimidazoles&#xD;
derived from secondary and primary amines. All the experimental data were statistically significant at P&amp;lt;0.05&#xD;
level.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1216-1219</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12673">
    <title>Synthesis and antibacterial activity of some novel &lt;i&gt;N&lt;/i&gt;-substituted 3-[4-(1-alkyl/acyl/aroyl-1&lt;i&gt;H&lt;/i&gt;-benzimidazol-2-yl)phenyl]acrylate derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12673</link>
    <description>Title: Synthesis and antibacterial activity of some novel &lt;i&gt;N&lt;/i&gt;-substituted 3-[4-(1-alkyl/acyl/aroyl-1&lt;i&gt;H&lt;/i&gt;-benzimidazol-2-yl)phenyl]acrylate derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Chaudhari, Raju B; Vaidya, Sanjay D; Karale, B K; Pawar, P Y; Rindhe, Sahebrao S
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of a series of novel 3-[4-(1-alkyl/acyl/aroyl-1&lt;i&gt;H&lt;/i&gt;-benzimidazol-2-yl)phenyl]acrylate&#xD;
derivatives has been reported.&#xD;
These derivatives are prepared by condensation of &lt;i style=""&gt;o&lt;/i&gt;-phenyle­nediamine with 4-bromobenzoic acid to give&#xD;
2-(4-bromophenyl)-1&lt;i&gt;H&lt;/i&gt;-benzimidazole which undergoes Heck reaction with&#xD;
alkyl acrylates to give the above benzimidazole derivatives. Subsequent reactions of these&#xD;
compounds with different types of electrophiles afford a series of the&#xD;
corresponding 1N-substituted alkyl/acyl/­aroyl/sulfonyl derivatives.&#xD;
Furthermore, the antibacterial activities of these compounds have been checked&#xD;
against &lt;i style=""&gt;Staphylococcus aureus&lt;/i&gt; and &lt;i style=""&gt;Salmonella typhimurium&lt;/i&gt; bacterial&#xD;
strains but the results are found to be disappointing.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1208-1215</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12672">
    <title>Synthesis and characterization and anti-inflammatory and antibacterial evaluation of 3-arylidene-7-methoxychroman-4-ones</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12672</link>
    <description>Title: Synthesis and characterization and anti-inflammatory and antibacterial evaluation of 3-arylidene-7-methoxychroman-4-ones
&lt;br/&gt;
&lt;br/&gt;Authors: Shankar, T; Gandhidasan, R; Venkataraman, S
&lt;br/&gt;
&lt;br/&gt;Abstract: 3-Arylidene-7-methoxychroman-4-ones&#xD;
&lt;b style=""&gt;3a-k&lt;/b&gt; have been prepared from&#xD;
7-methoxy-chroman-4-one &lt;b style=""&gt;1&lt;/b&gt; and heterocyclic&#xD;
aldehydes &lt;b style=""&gt;2&lt;/b&gt; and have been evaluated&#xD;
for anti-inflammatory and antibacterial activities. All of them have registered&#xD;
moderate anti-inflammatory and antibacterial activities.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1202-1207</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12671">
    <title>Synthesis and antibacterial activities of new dibenzothiazepine derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12671</link>
    <description>Title: Synthesis and antibacterial activities of new dibenzothiazepine derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Mahale, Ganesh D; Kolekar, Yogesh M; Kumar, Ashok; Singh, Dharmendra; Kodam, Kisan M; Waghmode, Suresh B
&lt;br/&gt;
&lt;br/&gt;Abstract: A number of substituted&#xD;
dibenzo[&lt;i style=""&gt;b,f&lt;/i&gt;][1,4]thiazepines&#xD;
analogues carrying heterocyclic and aliphatic moiety attached to C-11 position&#xD;
have been synthesized and evaluated their antibacterial activities against gram positive and gram negative&#xD;
bacteria. Derivatives of imidazole, 2-methyl imidazole and pyrrolidine exhibit&#xD;
significant antibacterial activities.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1196-1201</description>
  </item>
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