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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19755" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/19755</id>
  <updated>2026-10-08T20:35:29Z</updated>
  <dc:date>2026-10-08T20:35:29Z</dc:date>
  <entry>
    <title>Molecular structure-activity relationship study of some non-steroidal antiinflammatory agents using electrostatic potential mapping</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19832" />
    <author>
      <name>Mohan, C Gopi</name>
    </author>
    <author>
      <name>Mishra, PC</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19832</id>
    <updated>2013-07-22T16:38:27Z</updated>
    <published>2000-08-01T00:00:00Z</published>
    <summary type="text">Title: Molecular structure-activity relationship study of some non-steroidal antiinflammatory agents using electrostatic potential mapping
Authors: Mohan, C Gopi; Mishra, PC
Abstract: A series of 6, 11&#xD;
-dihydro-11-oxodibenz[b,e]oxepin-2-acetic acids (DOAA) which are known to be&#xD;
anti-inflammatory agents were studied. The geometries of some of the molecules&#xD;
obtained from X-ray crystallography were used in the calculations as such while&#xD;
the geometries of their derivatives were obtained by local, partial geometry&#xD;
optimization around&#xD;
&#xD;
the sites of substitution employing the AM1&#xD;
method, keeping the remaining parts of the geometries the same as those in the parent&#xD;
molecules. Molecular electrostatic potential (MEP) mapping was performed for&#xD;
the molecules using optimized hybridization displacement charges (HDC) combined&#xD;
with Lowdin charges, as this charge distribution has been shown&#xD;
&#xD;
earlier to yield near &lt;i&gt;ab initio &lt;/i&gt;quality&#xD;
results. A good correlation has been found between the MEP values near the&#xD;
oxygen atoms of the hydroxyl groups of the carboxy groups of the molecules and&#xD;
their anti-inflammatory activities. The result is broadly in agreement with the&#xD;
model proposed earlier by other authors regarding the structure-activity&#xD;
relationship for other&#xD;
&#xD;
similar molecules.
Page(s): 268-272</summary>
    <dc:date>2000-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Metal ion mediated inhibition of firefly bioluminescence: A possibility via a quaternary complex</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19831" />
    <author>
      <name>Sudhaharan, T</name>
    </author>
    <author>
      <name>Reddy, A Ram</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19831</id>
    <updated>2013-07-18T16:38:28Z</updated>
    <published>2000-08-01T00:00:00Z</published>
    <summary type="text">Title: Metal ion mediated inhibition of firefly bioluminescence: A possibility via a quaternary complex
Authors: Sudhaharan, T; Reddy, A Ram
Abstract: D(-) Luciferin, interacts with different&#xD;
metal ions to produce colourless soluble salts with absorption spectra broader,&#xD;
intense and red shifted as compared to those of the parent compound. The&#xD;
equilibrium constants for the luciferin-metal ion system vary in the order,&#xD;
depository divalent transition metal ions &gt; alkali metal ions. The&#xD;
equilibrium constants for the ternary complexes formed between metal ions and a&#xD;
mixture of lucifcrin and luciferase are larger than that of binary complexes&#xD;
but vary in the same order. Steady state fluorometric titration's of luciferin&#xD;
further confirmed its complexation with metal ions. The single absorption&#xD;
maximum of firefly luciferase at 278 nm originating from tyrosine was split&#xD;
into a doublet in presence of transition metal ions. The absorption maximum at&#xD;
lower wavelength is attributed to the H-bond raptured free tyrosine denatured&#xD;
conformation of the luciferase while the longer wavelength band to tyrosine-&#xD;
transition metal ion complex. Difference spectra of luciferase metal ion&#xD;
complex yielded change in the molar extinction coefficients from which the&#xD;
number of tyrosine molecules exposed to aqueous solution by the perturbant&#xD;
metal ions are evaluated following the Donovan model. The number of tyrosine&#xD;
molecules exposed to the aqueous medium as a result of conformational change in&#xD;
the enzyme are 4, 3, 3, 2 and 3 by Hg&lt;sup&gt;2+&lt;/sup&gt;,Mn&lt;sup&gt;2+&lt;/sup&gt;, Co&lt;sup&gt;2+&lt;/sup&gt;,&#xD;
Cd&lt;sup&gt;2+&lt;/sup&gt; and Cs&lt;sup&gt;+&lt;/sup&gt; respectively. The denaturation constants&#xD;
calculated for the luciferase-metal ion complexes vary between 0.152 and 0.570&#xD;
and follow the order of Hg&lt;sup&gt;2+&lt;/sup&gt;&gt; Cs&lt;sup&gt;+&lt;/sup&gt;&gt; Cd&lt;sup&gt;2+&lt;/sup&gt;&gt;&#xD;
Co&lt;sup&gt;2+&lt;/sup&gt;&gt; Mn&lt;sup&gt;2+&lt;/sup&gt;. Steady state fluorescence data reveal that&#xD;
the metal ions quench the fluorescence of enzyme by complexation with the side&#xD;
chain residues of the excited state tyro sine. Profound change in the UV CD&#xD;
spectrum of luciferin and luciferase in presence of metal ions was attributed&#xD;
to the conformational change in the substrate and enzyme. Thus the inhibition&#xD;
of luciferase activity in the firefly bioluminescence by metal ions is&#xD;
attributed to the quaternary complex formed between metal ion-luciferin-luciferase&#xD;
and ATP near or around the active site of the enzyme.
Page(s): 256-267</summary>
    <dc:date>2000-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>X-band electron paramagnetic resonance spectra of pig serum albumin-copper(II) and pig serum albumin-copper(II)-amino acid systems</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19830" />
    <author>
      <name>Patel, R N</name>
    </author>
    <author>
      <name>Pandeya, K B</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19830</id>
    <updated>2013-07-24T16:36:17Z</updated>
    <published>2000-08-01T00:00:00Z</published>
    <summary type="text">Title: X-band electron paramagnetic resonance spectra of pig serum albumin-copper(II) and pig serum albumin-copper(II)-amino acid systems
Authors: Patel, R N; Pandeya, K B
Abstract: EPR spectra of the binary, PSA-copper(II)&#xD;
(1:1 and 2:1) and ternary systems, PSA-copper(II) -amino acid (1:1:1) have been&#xD;
studied. In binary system, two distinct EPR features have been observed, one of&#xD;
the features (towards the low field), showing broad and overlapping signals is&#xD;
attributed to non-specific bonding of copper(II) to albumin and other feature&#xD;
(towards higher field), showing sharp intense signals is attributed to specific&#xD;
bonding. The change from non-specific to specific bonding is favoured by&#xD;
increase in &lt;i&gt;p&lt;/i&gt;H as well as by increase in protein concentration. Observed&#xD;
&lt;i&gt;p&lt;/i&gt;H for transition from non-specific binding is 10.00 &lt;&lt;i&gt;p&lt;/i&gt;H &lt;&#xD;
11.30. A better resolution of nitrogen hyperfine couplings are obtained for&#xD;
both binary, PSA-Cu(II) (1:1 and 2:1) and ternary PSA-Cu(II)-amino ac id&#xD;
(1:1:1) systems. Seven and more than seven nitrogen superhyperfine lines are&#xD;
observed in g  region of binary and&#xD;
ternary systems respectively.
Page(s): 251-255</summary>
    <dc:date>2000-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Dye-mediated photodynamic inactivation of &lt;i&gt;Bacillus subtilis &lt;/i&gt;cells: Involvement of singlet oxygen and superoxide radicals</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19829" />
    <author>
      <name>Dube, Alok</name>
    </author>
    <author>
      <name>Bansal, Harsha</name>
    </author>
    <author>
      <name>Gupta, Pradeep K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19829</id>
    <updated>2013-07-17T16:36:54Z</updated>
    <published>2000-08-01T00:00:00Z</published>
    <summary type="text">Title: Dye-mediated photodynamic inactivation of &lt;i&gt;Bacillus subtilis &lt;/i&gt;cells: Involvement of singlet oxygen and superoxide radicals
Authors: Dube, Alok; Bansal, Harsha; Gupta, Pradeep K
Abstract: Studies were carried out on the&#xD;
photodynamic inactivation of &lt;i&gt;Bacillus subtilis &lt;/i&gt;cells by He-Ne laser&#xD;
irradiation in presence of methylene blue and toluidine blue. Electron&#xD;
paramagnetic resonance (EPR) measurements show decrease in the cell membrane&#xD;
nuidity due to photodynamic damage of the lipophilic compartments. Study of&#xD;
cell damage in presence of sodium azide, D&lt;sub&gt;2&lt;/sub&gt;O and glutathione as well&#xD;
as measurements on singlet oxygen/free radical generation by EPR show that with&#xD;
toluidine blue, singlet oxygen is the major reactive species leading to cell&#xD;
membrane damage. No free radical generation was observed in toluidine blue&#xD;
mediated photodamage. However, with methylene blue our observations suggest&#xD;
that the photodamage arises due to both singlet oxygen mediated membrane damage&#xD;
and intracellular damage by superoxide radical.
Page(s): 245-250</summary>
    <dc:date>2000-08-01T00:00:00Z</dc:date>
  </entry>
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