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Articles 1 - 4 of 4
Full-Text Articles in Physical Sciences and Mathematics
Synthesis Of Some New Benzimidazole Carbamate Derivatives For Evaluation Of Antifungal Activity, Canan Kuş, Nurten Altanlar
Synthesis Of Some New Benzimidazole Carbamate Derivatives For Evaluation Of Antifungal Activity, Canan Kuş, Nurten Altanlar
Turkish Journal of Chemistry
The synthesis and structure elucidation of methyl 5(6)-fluoro-6(5)-substituted-1H-benzimidazole carbamate derivatives are performed and their antifungal activities evaluated against Candida albicans.
Synthesis, Characterization And Primary Antituberculosis Activity Evaluation Of 4-(3-Coumarinyl)-3-Benzyl-4-Thiazolin-2-One Benzylidenehydrazones, Aysel Gürsoy, Ni̇lgün Karali̇
Synthesis, Characterization And Primary Antituberculosis Activity Evaluation Of 4-(3-Coumarinyl)-3-Benzyl-4-Thiazolin-2-One Benzylidenehydrazones, Aysel Gürsoy, Ni̇lgün Karali̇
Turkish Journal of Chemistry
In this study a new series of 4-(3-coumarinyl)-3-benzyl-4-thiazolin- 2-one benzylidenehydrazones 3a-t was synthesized. Structures of the title compounds were elucidated by elemental analyses and spectrometric data (IR, ^1H-NMR, ^{13}C-NMR and EIMS). 3a-t were evaluated for antituberculosis activity against Mycobacterium tuberculosis} H37Rv in BACTEC 12B medium using the BACTEC 460 radiometric system.
Synthesis And Analgesic And Anti-Inflammatory Activity Of New Pyridazinones, Deni̇z S. Doğruer, M. Fethi̇ Şahi̇n, Esra Küpeli̇, Erdem Yeşi̇lada
Synthesis And Analgesic And Anti-Inflammatory Activity Of New Pyridazinones, Deni̇z S. Doğruer, M. Fethi̇ Şahi̇n, Esra Küpeli̇, Erdem Yeşi̇lada
Turkish Journal of Chemistry
A new series of 2-(6-oxo-3,5-diphenyl-6H-pyridazin-1-yl)- acetamides and 3-[6-oxo-3,5-diphenyl-6H-pyridazin-1-yl)-propanamides were synthesized and evaluated in terms of their analgesic and anti-inflammatory activities. All compounds except for 7g were more potent than aspirin in a p-benzoquinone--induced writhing test at 100 mg/kg dose. Compounds 7b, 7c and 7e had the highest anti-inflammatory activity; compound 7e was the most potent in terms of analgesic and anti-inflammatory activities and had no ulcerogenic side effects.
Synthesis And Antimicrobial Testing Of Some Flavonylsulfonamide Derivatives, Gülgün Ayhan Kilcigi̇l, Oya Bozdağ Dündar, Rahmi̇ye Ertan, Nurten Altanlar
Synthesis And Antimicrobial Testing Of Some Flavonylsulfonamide Derivatives, Gülgün Ayhan Kilcigi̇l, Oya Bozdağ Dündar, Rahmi̇ye Ertan, Nurten Altanlar
Turkish Journal of Chemistry
Six new 4-amino-N-heteroaryl,N-[(2-phenyl-4H-1-benzopyran-4- oxo-6-yl)metil]benzensulfonamide derivatives, (3a-3f) were prepared by reacting 6-bromomethylflavone with the corresponding sulfonamide derivatives and their antimicrobial activities against Escherichia coli were evaluated. All of the compounds exhibited better activity (except compound 3c) than the corresponding sulfonamide derivatives.