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<title>Indonesia Journal of Pharmacy Vol 27 no 4 Agustus-Desember 2016</title>
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<namePart>Indonesia J.Pharm</namePart>
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<place><placeTerm type="text">Jogjakarta</placeTerm></place>
<publisher>Universitas Gadjah Mada</publisher>
<dateIssued>2016</dateIssued>
<issuance>monographic</issuance>
<edition>Vol 27 no 4 Agustus-Desember 2016</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<form authority="gmd">Karya Tulis Ilmiah</form>
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<note>ABSTRACT
Several novel 2-[(substitutedphenyl)-5-(1-phenyl-3-
(piperazinyl) pyrido[3,2-f] quinazolin-4(1H)-yl]-1,3,4 thiadiazole
derivatives have been designed and synthesised by incorporating
four known moieties suchas 2-methylquinolin-5-ol, acetophenone,
urea and 3-substitutedphenyl-4-amino-5-mercapto triazoles by
using multi-step conventional reaction strategy. The synthesized
derivatives were characterized by IR, 1H-NMR, Mass and
elemental analysis (C, H, N). Furthermore the synthesized
2-[(substitutedphenyl)-5-(1-phenyl-3-(piperazinyl)pyrido[3,2-f]
quinazolin-4(1H)-yl]-1,3,4-thiadiazoles 4a-g were screened for
antibacterial and antifungal activities. The bacterial panel
consisted of Staphylococcus aureus, Escherichia coli, Klebsiella
pneumoniae, Proteus vulgaris while fungal panel included of
Aspergillus fumigatus (plant isolate), Candida glabrata, Candida
albicans, Candida krusei. Ampicillin trihydrate and fluconazole
were used as reference drugs for antibacterial and antifungal
activity, respectively. Bacterial and fungal inhibition determined
by disk diffusion and serial plates dilution method, respectively.
Pathogenic inhibitions were determined by measuring the
diameter of the inhibition zone in mm. Compound 4c
demonstrated significant antibacterial and antifungal spectrum
against all the tested microbes.
Keywords- antibacterial, antifungal and substituted 1,3,4-thiadiazoles</note>
<subject authority=""><topic>farmasi</topic></subject>
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<physicalLocation>PERPUSTAKAAN SEKOLAH TINGGI ILMU KESEHATAN SAMARINDA REPOSITORY</physicalLocation>
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