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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/61404">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61404</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/61416" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/61415" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/61414" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/61413" />
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    </items>
    <dc:date>2026-10-09T03:31:00Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/61416">
    <title>Synthesis of Schiff bases of 2-amino benzo[d]thiazole from higher hetero aldehydes and ketones using Mo-Al2O3 composite-based organocatalyst</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61416</link>
    <description>Title: Synthesis of Schiff bases of 2-amino benzo[d]thiazole from higher hetero aldehydes and ketones using Mo-Al2O3 composite-based organocatalyst
Authors: Anam, Koteswara Rao; Thirunarayanan, Ganesamoorthy
Abstract: A new metal supported organo catalyst has been successfully employed to carry out the high yield Schiff’s base reaction&#xD;
at ambient temperature. This methodology has the benefits of straightforward conditions, excellent yields, no work-up,&#xD;
environmental benign process and reusable solid catalyst. The catalyst speeds up the Schiff base reaction with less time and&#xD;
several Schiff bases have been synthesized and characterized with IR, 1H and 13C NMR techniques.
Page(s): 91-98</description>
    <dc:date>2023-02-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/61415">
    <title>Microwave-assisted solution phase synthesis of novel pyridine carboxamides in neat water and ADMET and protein-compounds interaction analysis and antibacterial activity</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61415</link>
    <description>Title: Microwave-assisted solution phase synthesis of novel pyridine carboxamides in neat water and ADMET and protein-compounds interaction analysis and antibacterial activity
Authors: Babu, Visagamoorthy; Dharman, Prabu; Basha, K Anver
Abstract: A range of novel 5-substituted-pyridine-2-carboxamides have been designed and synthesized by microwave-assisted&#xD;
solution phase synthesis in neat water. Their structures have been confirmed by 1H NMR, 13C NMR and LCMS analysis.&#xD;
The present work describes a simple, rapid, and efficient synthesis of compound 2a-2h in good yield under mild reaction&#xD;
condition. Shorter reaction time and convenient workup make this methodology more practical. This protocol proceeds&#xD;
smoothly and avoids the use of toxic organic solvents. ADMET analysis have been performed for all the synthesized&#xD;
compounds and observed that all the eight compounds taken for the investigation have been shown to satisfy Lipinski's rule&#xD;
of 5. The molecular interaction study is performed using the AutoDock software. All the 8 test compounds are found to have&#xD;
higher binding affinity than the control compound chloramphenicol to the E. Coli DraE adhesion. In addition antibacterial&#xD;
activities of all eight compounds have been determined.
Page(s): 99-106</description>
    <dc:date>2023-02-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/61414">
    <title>Ru(II)/PEG-400: A green synthesis of indolyl-oxindoles and indolyl-cyclohexanedione hybrids as potential antimicrobial agents</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61414</link>
    <description>Title: Ru(II)/PEG-400: A green synthesis of indolyl-oxindoles and indolyl-cyclohexanedione hybrids as potential antimicrobial agents
Authors: Wagh, Shaila S; Patil, Arvind M; Kasralikar, Hanmant M
Abstract: A green and sustainable methodology has been successfully employed for the synthesis of 3-Indolyl-3-hydroxy&#xD;
oxindoles and 3-indolyl-3-hydroxy-5,5-dimethylcyclohexane-1,3-dione derivatives using Ru(II)/PEG-400 as a homogeneous&#xD;
recyclable catalytic system from substituted isatin with indole and dimedone. Short reaction time, simple extraction&#xD;
procedure, substrate scope with high yield of the product, biodegradable solvent and recyclability of the catalyst without loss&#xD;
of its activity enhances the efficiency of the proposed protocol. The synthesized compounds are studied for their&#xD;
antimicrobial activity.
Page(s): 107-114</description>
    <dc:date>2023-02-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/61413">
    <title>Synthesis and bio-evaluation of novel acyl derivatives of karanjin</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61413</link>
    <description>Title: Synthesis and bio-evaluation of novel acyl derivatives of karanjin
Authors: Eanti, Anjaneyulu; Kuncha, Madhusudana; Arundha, Ande; Misra, Sunil; Vidavalur, Siddaiah; Ramakrishna, Sistla; Kanjilala, Sanjit
Abstract: Different lipidic moieties such as 10-undecenoic, oleic, lipoic, caproic, caprylic and lauric acids have been acylated to&#xD;
demethylated karanjin to prepare six lipoconjugated karanjin. All the derivatives have been evaluated for antimicrobial,&#xD;
anticancer and antiinflammatory activities and compared with karanjin and its demethylated analog. Lipoconjugation does&#xD;
not seem to improve the activity of karanjin against studied bacterial and fungal strains. However, karanjin, demethylated&#xD;
karanjin and six lipoconjugated karanjin show moderate to good anticancer activity against prostate and breast cancer cell&#xD;
lines. Mild antiinflammatory response has also been observed in case of karanjin and lipoic acid-conjugated karanjin.
Page(s): 115-120</description>
    <dc:date>2023-02-01T00:00:00Z</dc:date>
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