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dc.contributor.authorHiba Maher Tawfeeq, Rasim Farraj Muslim-
dc.contributor.authorObaid Hasan Abid, Mustafa Nadhim Owaid-
dc.date.accessioned2022-10-12T19:34:08Z-
dc.date.available2022-10-12T19:34:08Z-
dc.date.issued2019-
dc.identifier.issn1307-2080-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/181-
dc.description.abstractThis research includes synthesis of new heterocycles containing disubstituted Tetrazole derivatives. Imine compounds were synthesized by reaction of primary aromatic amines with various substituted benzaldehydes in the presence of gla cial acetic acid as catalyst in absolute ethanol to obtain new imine compounds O1 -O5 . The novel five-membered heterocycles as Tetrazole derivatives O6 -O10 were obtained from treatment of each new imine compounds with sodium azide com pound. Newly synthesized compounds were identified via spectral methods (FT IR, 1 H-NMR and 13C-NMR) spectra and some physical properties. O6 is the best derivative that has significantly (p<0.01) recorded a stronger influence to inhibit the growth of Candida guilliermondii at an average of the zone of inhibition 14.0 mm. While, O9 derivative recorded the lowest zone of inhibition 7.3 mm toward the same clinical fungal pathogen. The present work may be helpful in designing more potential antibacterial and antifungal agents for therapeutic use in the futureen_US
dc.language.isoenen_US
dc.publisherActa Pharmaceutica Scienciaen_US
dc.subjectTetrazoleen_US
dc.subjectCandida spen_US
dc.subjectanti-candidalen_US
dc.subjectimine compoundsen_US
dc.subjectsodium azideen_US
dc.titleSynthesis and Characterization of Novel Tetrazole Derivatives and Evaluation of Their Anti-candidal Activityen_US
dc.typeArticleen_US
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