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    <pubDate>Sat, 04 Apr 2026 03:10:19 GMT</pubDate>
    <dc:date>2026-04-04T03:10:19Z</dc:date>
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      <title>Preparation, characterization and tissue disposition of niosomes containing isoniazid</title>
      <link>http://13.232.72.61:8080/jspui/handle/123456789/6289</link>
      <description>Title: Preparation, characterization and tissue disposition of niosomes containing isoniazid
Authors: Karki, Roopa; Mamatha, GC; Subramanya, G.; Udupa, N</description>
      <pubDate>Tue, 01 Apr 2008 00:00:00 GMT</pubDate>
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      <dc:date>2008-04-01T00:00:00Z</dc:date>
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      <title>Synthesis and antimicrobial activity of Some Novel Chalcones Containing 3-Hydroxy Benzofuran</title>
      <link>http://13.232.72.61:8080/jspui/handle/123456789/6288</link>
      <description>Title: Synthesis and antimicrobial activity of Some Novel Chalcones Containing 3-Hydroxy Benzofuran
Authors: Gurubasavarajaswamy, PM; Agasimunddin, YS
Abstract: 2-Acetyl-3-hydroxy benzofuran were allowed to react separately with different aromatic aldehydes in presence of 50% alkaline medium to yield the corresponding 3-hydroxy benzofuran substituted chalcones. The compounds obtained were identified by spectral data and screened for antimicrobial activity.</description>
      <pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
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      <dc:date>2008-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Synthesis and antimicrobial activity of isoxazolines bearing Hydroxybenzofuran.</title>
      <link>http://13.232.72.61:8080/jspui/handle/123456789/6287</link>
      <description>Title: Synthesis and antimicrobial activity of isoxazolines bearing Hydroxybenzofuran.
Authors: Gurubasavarajaswamy, PM; Agasimunddin, YS
Abstract: 3-Hydroxy Bezofuran Chalcones (2a-g) prepared by the reaction of 2-acetyl-3-hydroxybenzofuran(1) with&#xD;
different aromatic aldehydes in the presence of a strong base, cyclocondensation of 3-Hydroxy&#xD;
benzofuran with hydroxlaminehydrochloride resulted in the formation of various Isoxazolines bearing&#xD;
hydroxyl benzofuran (3a-f). The structures of all the compounds have been established on the basis of&#xD;
analytical and spectral data. All the compounds have screened for antibacterial, while compounds&#xD;
2a,2c,3a,3b, showed only moderate activity against staphylococcus at 500 mg/ml, compounds 2d, 2f, 3d,&#xD;
3e, showed promising activity against Candida albicans at 500mg/ml concentration.
Description: Articles</description>
      <pubDate>Tue, 01 Apr 2008 00:00:00 GMT</pubDate>
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      <dc:date>2008-04-01T00:00:00Z</dc:date>
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      <title>Synthesis and Antimicrobial Activity of Some Novel Substituted Piperazinyl-quinazolin-3(4H)-ones</title>
      <link>http://13.232.72.61:8080/jspui/handle/123456789/6286</link>
      <description>Title: Synthesis and Antimicrobial Activity of Some Novel Substituted Piperazinyl-quinazolin-3(4H)-ones
Authors: Raghavendra, N M; Thampi, P P; Gurubasavarajaswamy, P M
Abstract: Several substituted-quinazolin-3(4H)-ones were synthesized by&#xD;
condensation of 2-chloro-N-(4-oxo-substituted-quinazolin-3(4H)-yl)-acetamides&#xD;
with various substituted piperazines through single step reaction. Elemental&#xD;
analysis, IR, 1HNMR and mass spectral data confirmed the structure of the newly&#xD;
synthesized compounds. Synthesized quinazolin-4-one derivatives were&#xD;
investigated for their antibacterial and antifungal activities.</description>
      <pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
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      <dc:date>2008-01-01T00:00:00Z</dc:date>
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