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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.50B(02) [February 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/11026</link>
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      <title>Synthesis and antimicrobial activity of bis-[2-imino-3-[5-(3-methylbenzo[&lt;i&gt;b&lt;/i&gt;]furan-7-yl)-1,3,4-thiadiazol-2-yl]-5-(arylidene)-1,3-thiazolan-4-one]methanes</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11036</link>
      <description>Title: Synthesis and antimicrobial activity of bis-[2-imino-3-[5-(3-methylbenzo[&lt;i&gt;b&lt;/i&gt;]furan-7-yl)-1,3,4-thiadiazol-2-yl]-5-(arylidene)-1,3-thiazolan-4-one]methanes
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, Ch Sanjeeva; Rao, D Chandrashekar; Yakub, V; Nagaraj, A
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of novel bis-[2-imino-3-[5-(3-methylbenzo[&lt;i&gt;b&lt;/i&gt;]furan-7-yl)-1,3,4-thiadiazol-2-yl]-5-(arylidene)-1,3-thiazolan-4-one]­me­th-&#xD;
anes &lt;b&gt;6a-j&lt;/b&gt; have been prepared and their structures confirmed by&#xD;
IR, NMR, MS and elemental analyses. All the synthesized compounds have been&#xD;
tested for their antimicrobial activity against Gram-positive and Gram-negative&#xD;
bacteria, and fungi. Among the synthesized compounds, &lt;b style=""&gt;6c&lt;/b&gt;, &lt;b style=""&gt;6e&lt;/b&gt;, &lt;b style=""&gt;6f&lt;/b&gt;&#xD;
and &lt;b style=""&gt;6g&lt;/b&gt; are found to be the most&#xD;
active against &lt;i style=""&gt;Bacillus subtilis&lt;/i&gt;, &lt;i style=""&gt;Bacillus sphaericus&lt;/i&gt;, &lt;i style=""&gt;Staphylococcus aureus&lt;/i&gt;, &lt;i style=""&gt;Klebsiella aerogenes&lt;/i&gt; and &lt;i style=""&gt;Chromo­bacterium violaceum&lt;/i&gt;. Similarly,&#xD;
these compounds show potent antifungal effect against &lt;i style=""&gt;Candida albicans&lt;/i&gt;, &lt;i style=""&gt;Aspergillus&#xD;
fumigatus&lt;/i&gt;, &lt;i style=""&gt;Trichophyton rubrum&lt;/i&gt;,&#xD;
and &lt;i style=""&gt;Trichophyton mentagrophytes&lt;/i&gt;.
&lt;br/&gt;
&lt;br/&gt;Page(s): 253-259</description>
      <pubDate>Sat, 29 Jan 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>An efficient one-pot three component synthesis of new isoxazolyl polyhydroacridine-1,8-diones in an ionic liquid medium</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11035</link>
      <description>Title: An efficient one-pot three component synthesis of new isoxazolyl polyhydroacridine-1,8-diones in an ionic liquid medium
&lt;br/&gt;
&lt;br/&gt;Authors: Rajanarendar, E; Reddy, M Nagi; Shaik, Firoz Pasha
&lt;br/&gt;
&lt;br/&gt;Abstract: A facile and convenient&#xD;
protocol has been developed for the fast and high yielding one-pot three&#xD;
component synthesis of isoxazolyl polyhydroacridine-1,8-diones from dimedone,&#xD;
aromatic aldehyde and isoxazolyl amine in the presence of ionic liquid [bmim]&lt;sup&gt;+&lt;/sup&gt;BF&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt;&#xD;
as an efficient recyclable medium.
&lt;br/&gt;
&lt;br/&gt;Page(s): 245-252</description>
      <pubDate>Sat, 29 Jan 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of 4-(substituted benzyl)-1&lt;i style=""&gt;H&lt;/i&gt;,3&lt;i style=""&gt;H&lt;/i&gt;-benzo[&lt;i style=""&gt;f&lt;/i&gt;]1,3,5-triazepin-2-ones</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11034</link>
      <description>Title: Synthesis of 4-(substituted benzyl)-1&lt;i style=""&gt;H&lt;/i&gt;,3&lt;i style=""&gt;H&lt;/i&gt;-benzo[&lt;i style=""&gt;f&lt;/i&gt;]1,3,5-triazepin-2-ones
&lt;br/&gt;
&lt;br/&gt;Authors: Maruthikumar, T Venkata; Rao, G V Panakala; Reddy, V Prabhakar; Rao, P Hanumantha
&lt;br/&gt;
&lt;br/&gt;Abstract: This paper presents the&#xD;
synthesis of 4-(substituted benzyl)-1&lt;i style=""&gt;H&lt;/i&gt;,3&lt;i style=""&gt;H&lt;/i&gt;-benzo[&lt;i style=""&gt;f&lt;/i&gt;]1,3,5-triazepin-2-ones &lt;b style=""&gt;3&lt;/b&gt;&#xD;
from &lt;i style=""&gt;o&lt;/i&gt;-phenylenedi- amines &lt;b&gt;1&lt;/b&gt;&#xD;
and 4-(arylmethylene)-6-phenyl-3&lt;i style=""&gt;H&lt;/i&gt;-1,3,5-oxadiazin-2-ones&#xD;
&lt;b&gt;2&lt;/b&gt;.
&lt;br/&gt;
&lt;br/&gt;Page(s): 242-244</description>
      <pubDate>Sat, 29 Jan 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis and antimalarial activity of novel N-{2-[2-(2-aminoethoxy) ethoxy] ethyl}-7-chloroquinolin-4-amine and its derivatives</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11033</link>
      <description>Title: Synthesis and antimalarial activity of novel N-{2-[2-(2-aminoethoxy) ethoxy] ethyl}-7-chloroquinolin-4-amine and its derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Tanwar, Pooja; Yadav, Gyan Chand; Jaitley, U K; Kaushik, Naveen; Sahal, Dinkar
&lt;br/&gt;
&lt;br/&gt;Abstract: A number of N-{2-[2-(2-aminoethoxy)ethoxy]ethyl}-7-chloroquinolin-4-amine&#xD;
derivatives have been prepared by condensation of N-{2-[2-(2-aminoethoxy)&#xD;
ethoxy] ethyl}-7-chloroquinolin-4-amine with substituted aldehyde. The newly&#xD;
synthesized compounds have been characterized by IR, ¹H and ¹³C NMR, and mass&#xD;
spectral data. These compounds have been screened for &lt;i style=""&gt;in vitro&lt;/i&gt; antimalarial activity using the Sybr Green assay of &lt;i style=""&gt;P. falciparum&lt;/i&gt; in culture and the heme&#xD;
detoxification based Heme-HRP assay. Among these, compounds&#xD;
7-chloro-N-[2-(2-{2-[(2, 4-difluorobenzyl) amino] ethoxy} ethoxy) ethyl]&#xD;
quinolin-4-amine is found to be&#xD;
the most effective with IC&lt;sub&gt;50&lt;/sub&gt; value 60 &lt;img src='/image/spc_char/micro.gif' border=0&gt;M (in Heme-HRP assay) and 48&#xD;
nM (in &lt;i&gt;P. falciparum&lt;/i&gt; culture assay). These values compare well with the&#xD;
potency of chloroquine in the respective assays.
&lt;br/&gt;
&lt;br/&gt;Page(s): 233-241</description>
      <pubDate>Sat, 29 Jan 2011 22:58:59 GMT</pubDate>
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