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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22260</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 02:21:30 GMT</pubDate>
    <dc:date>2026-10-10T02:21:30Z</dc:date>
    <item>
      <title>Direct observation and structural investigation of galactomannans by transmission electron microscope</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/22581</link>
      <description>Title: Direct observation and structural investigation of galactomannans by transmission electron microscope
Authors: Yongli, Yang; Shoujun, Guo; Kun, Sun; Ji, Zhang; Tianzhen, Ju; Jian, Yao
Abstract: Galactomannans isolated from the seeds of&#xD;
&lt;i&gt;Ceratonia siliqua, Itelicise tetragonoloba &lt;/i&gt;and &lt;i&gt;Sophora japonica &lt;/i&gt;have&#xD;
been studied&lt;i&gt; &lt;/i&gt;directly by transmission electron microscope and the fine structures&lt;i&gt;&#xD;
&lt;/i&gt;of these galactomannans investigated. Although all the three&lt;i&gt; &lt;/i&gt;types&#xD;
of galactomannans are linear, they can be distinguished&lt;i&gt; &lt;/i&gt;from one another&#xD;
easily under transmission electron microscope. The results indicate that the&#xD;
fine structures of galactomannans&lt;i&gt; &lt;/i&gt;vary with their origin. Generally,&#xD;
galactomannan from guar is&lt;i&gt; &lt;/i&gt;non block-type, their α-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-galactose side-chains&#xD;
are disposed basically&lt;i&gt; &lt;/i&gt;regular; but not unifonnly. Unlike guar gum, the&#xD;
galactomannans&lt;i&gt; &lt;/i&gt;from sophora bean gum and locust bean gum have&lt;i&gt; &lt;/i&gt;block-type&#xD;
dispositions which are composed of alternately distributed&lt;i&gt; &lt;/i&gt;smooth zone&#xD;
and hair zone but the smooth zone of locust&lt;i&gt; &lt;/i&gt;bean gum is longer than that&#xD;
sophora bean gum.
Page(s): 313-316</description>
      <pubDate>Sat, 01 Apr 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/22581</guid>
      <dc:date>2000-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Steroidal alkaloids from &lt;i&gt;Veratrum taliense&lt;/i&gt;</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/22580</link>
      <description>Title: Steroidal alkaloids from &lt;i&gt;Veratrum taliense&lt;/i&gt;
Authors: Zhou, C X; Tan, R X; Ye, W C; Min, Z D
Abstract: Phytochemical reinvestigation of the&#xD;
roots and rhizomes of &lt;i&gt;Veratrum taliense &lt;/i&gt;yield three known (solanidine,veramiline-3-&lt;i&gt;O&lt;/i&gt;-β-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-glucopyranoside and stenophylline B-3-&lt;i&gt;O&lt;/i&gt;-β-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-glucopyranoside) and two novel steroidal&#xD;
alkaloids. The structures of the new compounds have been established by a&#xD;
combination of spectroscopic methods as 3- angeloylzygadenine-β-&lt;i&gt;N&lt;/i&gt;-oxide&#xD;
and (20&lt;i&gt;S&lt;/i&gt;, 25&lt;i&gt;S&lt;/i&gt;)-22,26-epiminocholesta-5,22-diene-3β,12α-diol&#xD;
(named veramitaline). The chemotaxonomic significance of the isolates are&#xD;
discussed briefly.
Page(s): 283-286</description>
      <pubDate>Sat, 01 Apr 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/22580</guid>
      <dc:date>2000-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A novel naphthalene glucoside from &lt;i&gt;Cassia javanica &lt;/i&gt;stem bark</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/22517</link>
      <description>Title: A novel naphthalene glucoside from &lt;i&gt;Cassia javanica &lt;/i&gt;stem bark
Authors: Sanghi, Rashmi; Singh, Rahul; Singh, J
Abstract: A new glucoside, 3-carbomethoxynaphtho [1,2-&lt;i&gt;b&lt;/i&gt;]-3',3'dimethylpyran-4-&lt;i&gt;O&lt;/i&gt;-,&lt;i&gt;β&lt;/i&gt;-glucopyranoside&#xD;
has been isolated from the stem bark of &lt;i&gt;Cassia javanica.&lt;/i&gt;
Page(s): 321-322</description>
      <pubDate>Sat, 01 Apr 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/22517</guid>
      <dc:date>2000-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis and antimicrobial activity of 2-substituted-6-chloro-8-nitro-4-trichloromethyl-4&lt;i&gt;H&lt;/i&gt;-1,3,2-benzodioxaphosphorin 2-oxides</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/22516</link>
      <description>Title: Synthesis and antimicrobial activity of 2-substituted-6-chloro-8-nitro-4-trichloromethyl-4&lt;i&gt;H&lt;/i&gt;-1,3,2-benzodioxaphosphorin 2-oxides
Authors: Srinivasulu, D; Reddy, C Devendranath
Abstract: A series of 2-aryloxy/2-arylthio-6-chloro-8-nitro-4-trichloromethyl-4&lt;i&gt;H&lt;/i&gt;-1,3,2-benzodioxaphosphorin&#xD;
2-oxides &lt;b&gt;3&lt;/b&gt; have been synthesized by-reacting 2-(2,2,,2-trichloro-1-hydroxyethyl)-4-chloro-6-nitrophenol&#xD;
&lt;b&gt;1&lt;/b&gt; with different arylphosphorodichloridates &lt;b&gt;2&lt;/b&gt; in the presence of triethylamine&#xD;
at 70-80°C. Some of these compounds are prepared by reacting the monochloride, 2-chloro-&#xD;
6-chloro-8-nitro-4-trichloromethyl-4&lt;i&gt;H&lt;/i&gt;-1, 3, 2-benzodioxaphosphorin 2-oxide&#xD;
4, &lt;i&gt;in situ &lt;/i&gt;with substituted phenol and thiols &lt;b&gt;5&lt;/b&gt;. The&#xD;
&#xD;
monochloride is prepared by condensing 2-(2,2,2-trichloro-1-hydroxyethyl)-&#xD;
4-chloro-6-nitrophenol with phosphorus oxychloride. IR, &lt;sup&gt;1&lt;/sup&gt;H, &lt;sup&gt;13&lt;/sup&gt;C&#xD;
and &lt;sup&gt;31&lt;/sup&gt;P NMR and mass spectral data have been discussed. Some of these&#xD;
compounds have been screened for their antibacterial and antifungal activities.
Page(s): 317-320</description>
      <pubDate>Sat, 01 Apr 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/22516</guid>
      <dc:date>2000-04-01T00:00:00Z</dc:date>
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