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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21472" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/21472</id>
  <updated>2026-10-10T01:12:43Z</updated>
  <dc:date>2026-10-10T01:12:43Z</dc:date>
  <entry>
    <title>Isolation and characterization of pectic polysaccharides from the fruits of &lt;i&gt;Naringi crenulata&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21543" />
    <author>
      <name>Mondal, Saroj K</name>
    </author>
    <author>
      <name>Ray, Bimalendu</name>
    </author>
    <author>
      <name>Thakur, Swapnadip</name>
    </author>
    <author>
      <name>Ghosal, Pradyot K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21543</id>
    <updated>2013-10-05T16:34:07Z</updated>
    <published>2003-02-01T00:00:00Z</published>
    <summary type="text">Title: Isolation and characterization of pectic polysaccharides from the fruits of &lt;i&gt;Naringi crenulata&lt;/i&gt;
Authors: Mondal, Saroj K; Ray, Bimalendu; Thakur, Swapnadip; Ghosal, Pradyot K
Abstract: Pectic polysaccharides have been isolated&#xD;
from the fruits of &lt;i&gt;Naringi crenulata &lt;/i&gt;by extraction with water. The water&#xD;
extract contains large amount of protein. The polymers present in the&#xD;
&#xD;
water extract are fractionated by graded&#xD;
precipitation with ethanol, anion exchange chromatography, and size exclusion chromatography.&#xD;
Characterization or the subtractions obtained therefrom by various chemical and&#xD;
physico-chemical methods of analysis reveals that the water extract contain&#xD;
pectic polymers substituted to various degrees with side chains comprising&#xD;
mainly or terminal, 1,4-, 1,6-, 1,3,6-linked galactose, together with lesser&#xD;
&#xD;
amounts of 1,2,4- and 1,3-linked&#xD;
galactose residues. Arabinose residues are terminal, 1, 5-, 1,3,5-linked. These&#xD;
polymers contain acetyl groups and give viscous solution in water.
Page(s): 437-442</summary>
    <dc:date>2003-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>New flavonoid glycosides from &lt;i&gt;Cassia occidentalis&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21541" />
    <author>
      <name>Purwar, Chhavi</name>
    </author>
    <author>
      <name>Rai, Renu</name>
    </author>
    <author>
      <name>Srivastava, Nidhi</name>
    </author>
    <author>
      <name>Singh, J</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21541</id>
    <updated>2013-10-04T16:36:33Z</updated>
    <published>2003-02-01T00:00:00Z</published>
    <summary type="text">Title: New flavonoid glycosides from &lt;i&gt;Cassia occidentalis&lt;/i&gt;
Authors: Purwar, Chhavi; Rai, Renu; Srivastava, Nidhi; Singh, J
Abstract: Two flavonoid glycosides&#xD;
3,2’-dihydroxy-7,8,4&lt;i&gt;'&lt;/i&gt; –trimethoxy-flavone-5-&lt;i&gt;O&lt;/i&gt;- {β-D-glucopyranosyl (1→2)}-β-D-galactopyranoside &lt;b&gt;1&lt;/b&gt;&#xD;
and apigenin-7-&lt;i&gt;O&lt;/i&gt;-β-D-allopyrano-side&#xD;
&lt;b&gt;2&lt;/b&gt; have been isolated from the plant of &lt;i&gt;Cassia occidentalis.&lt;/i&gt; The&#xD;
structures have been&#xD;
&#xD;
established on the basis of chemical&#xD;
evidences and spectroscopic method.
Page(s): 434-436</summary>
    <dc:date>2003-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>1-(2', 6'-Dihydroxyphenyl)-β-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-glucopyranoside, a novel C-glycoside from &lt;i&gt;Pterocarpus &lt;/i&gt;&lt;i&gt;marsupium&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21539" />
    <author>
      <name>Suri, K A</name>
    </author>
    <author>
      <name>Satti, N K</name>
    </author>
    <author>
      <name>Gupta, B D</name>
    </author>
    <author>
      <name>Suri, O P</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21539</id>
    <updated>2013-10-04T16:35:26Z</updated>
    <published>2003-02-01T00:00:00Z</published>
    <summary type="text">Title: 1-(2', 6'-Dihydroxyphenyl)-β-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-glucopyranoside, a novel C-glycoside from &lt;i&gt;Pterocarpus &lt;/i&gt;&lt;i&gt;marsupium&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;&lt;/span&gt;
Authors: Suri, K A; Satti, N K; Gupta, B D; Suri, O P
Abstract: Isolation and characterisation of a novel&#xD;
C-glycoside from&#xD;
&lt;i&gt;Pt&lt;/i&gt;&lt;i&gt;e&lt;/i&gt;&lt;i&gt;r&lt;/i&gt;&lt;i&gt;oca&lt;/i&gt;&lt;i&gt;rpu&lt;/i&gt;&lt;i&gt;s &lt;/i&gt;&lt;i&gt;mar&lt;/i&gt;&lt;i&gt;s&lt;/i&gt;&lt;i&gt;upium &lt;/i&gt;Roxb.&#xD;
(Leguminosae)&#xD;
is reported. The isolate coded as&#xD;
VS002 &lt;b&gt;1&lt;/b&gt;, has been characterised as 1-(2&lt;i&gt;'&lt;/i&gt;, 6&lt;i&gt;'&lt;/i&gt; dihydroxyphenyl)-β-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-glucopyranoside on the basis&#xD;
of spectroscopic data and derivatisation.
Page(s): 432-433</summary>
    <dc:date>2003-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Microwave assisted acetylation and deacetylation studies on the triterpenes isolated from &lt;i&gt;Dysoxylum malabaricum &lt;/i&gt;and &lt;i&gt;Dysoxylum beddomei&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21530" />
    <author>
      <name>Jayakumar, G</name>
    </author>
    <author>
      <name>Ajithabai, M D</name>
    </author>
    <author>
      <name>Santhosh, B</name>
    </author>
    <author>
      <name>Veena, C S</name>
    </author>
    <author>
      <name>Nair, Mangalam S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21530</id>
    <updated>2013-10-05T16:34:39Z</updated>
    <published>2003-02-01T00:00:00Z</published>
    <summary type="text">Title: Microwave assisted acetylation and deacetylation studies on the triterpenes isolated from &lt;i&gt;Dysoxylum malabaricum &lt;/i&gt;and &lt;i&gt;Dysoxylum beddomei&lt;/i&gt;
Authors: Jayakumar, G; Ajithabai, M D; Santhosh, B; Veena, C S; Nair, Mangalam S
Abstract: Phytochemical investigations on the&#xD;
leaves of &lt;i&gt;Dysoxylum malabaricum &lt;/i&gt;and &lt;i&gt;Dysoxylum beddomei &lt;/i&gt;result in the&#xD;
isolation of a&lt;i&gt; &lt;/i&gt;number of triterpenes. Acetylation and deacetylation studies&#xD;
on&lt;i&gt; &lt;/i&gt;some of the representative triterpenes show appreciable rate enhancement&#xD;
&#xD;
and increase of yield in the presence of microwave&#xD;
radiation. Details of isolation of triterpenes, acetylation and deacetylation procedures&#xD;
and their results form the subject of the paper. Triterpenes of three skeletal types&#xD;
namely lupane, tirucallane and cycloartane are examined. All the triterpenes&#xD;
examined indicate an increase of cytotoxicity with acetylation.
Page(s): 429-431</summary>
    <dc:date>2003-02-01T00:00:00Z</dc:date>
  </entry>
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