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Articles 1 - 5 of 5
Full-Text Articles in Physical Sciences and Mathematics
Synthesis Of Some New 1-Acylthiosemicarbazides And 1,2,4-Triazol-5-Thiones, And Their Analgesic And Anti-Inflammatory Activities, Yasemi̇n Dündar, Bi̇lge Çakir, Esra Küpeli̇, M. Fethi̇ Şahi̇n, Ni̇ngur Noyanalpan
Synthesis Of Some New 1-Acylthiosemicarbazides And 1,2,4-Triazol-5-Thiones, And Their Analgesic And Anti-Inflammatory Activities, Yasemi̇n Dündar, Bi̇lge Çakir, Esra Küpeli̇, M. Fethi̇ Şahi̇n, Ni̇ngur Noyanalpan
Turkish Journal of Chemistry
We synthesized new 1-[3-(2-oxobenzothiazolin-3-yl)propanoyl]-4- substituted-thiosemicarbazides and their corresponding cyclized 3-[2-(2-oxobenzothiazoline-3-yl)ethyl]-4-substituted-1,2,4-triazol-5-thione ana-logs in which position 4 of the triazole ring was substituted by cyclohexyl, methyl, allyl, phenyl, p-methylphenyl, p-methoxyphenyl, p-chlorophenyl, p-nitrophenyl, benzyl, and phenylethyl to screen their analgesic and anti-inflammatory activities as well as gastric ulceration potential in test animals. None of the compounds, except 5a, 5e, and 5h, caused gastric lesions or bleeding. Compound 5g was found to have higher analgesic and anti-inflammatory activity among the synthesized compounds.
Preconcentration Of Trace Elements On Amberlite Xad-4 Resin Functionalised With 1,2-Bis (O-Aminophenylthio) Ethane And Their Determination By Faas In Environmental Samples, Ömer Dalman, Volkan Numan Bulut, İsmai̇l Deği̇rmenci̇oğlu, Mehmet Tüfekçi̇
Preconcentration Of Trace Elements On Amberlite Xad-4 Resin Functionalised With 1,2-Bis (O-Aminophenylthio) Ethane And Their Determination By Faas In Environmental Samples, Ömer Dalman, Volkan Numan Bulut, İsmai̇l Deği̇rmenci̇oğlu, Mehmet Tüfekçi̇
Turkish Journal of Chemistry
The use of chemically modified XAD-4-1,2-bis (o-aminophenylthio) ethane chelating resin for preconcentrating Cr^{6+}, Mn^{2+}, Fe^{3+}, Co^{2+}, Cu^{2+}, Cd^{2+}, Zn^{2+}, Pb^{2+}, and Ni^{2+} was studied using flame atomic absorption spectrometry (FAAS) for metal monitoring in environmental samples. Cd^{2+}, Zn^{2+}, Pb^{2+}, and Ni^{2+} ions were quantitatively recovered at the rate of 96.0%, 101.0%, 101.0%, and 95.0%, respectively (RSD < 5%), from the studied solutions. The procedure is based on the retention of analytes on a short column of 1,2-bis (o-aminophenylthio) ethane-XAD-4 chelating resin from a buffered sample solution and subsequent elution with 1 M HNO_3. Various parameters, such as pH, eluent type, and concentration, flow rate of sample solution and matrix interference effect on the retention of the metal ions have been studied. The optimum pH for the sorption of the above-mentioned metal ions was about 6. The adsorption and batch capacity of adsorbent and loading half time (t_{1/2}) for Ni^{2+}, Zn^{2+}, Cd^{2+}, and Pb^{2+} were established. The limit of detection was 3.0 \mu g L^{-1} for Pb^{2+} and Ni^{2+}, 0.6 \mu g L^{-1} for Cd^{2+}, and 0.3 \mu g L^{-1} for Zn^{2+}. The validation of the procedure was carried out by analysis of certified reference materials and standard addition. The proposed enrichment method was applied to environmental samples from Trabzon.
Synthesis Of 2-Acylamino, 2-Aroylamino And Ethoxycarbonyl Imino-1,3,4-Thiadiazoles As Antitumor Agents, Kemal Sancak, Yasemi̇n Ünver, Mustafa Er
Synthesis Of 2-Acylamino, 2-Aroylamino And Ethoxycarbonyl Imino-1,3,4-Thiadiazoles As Antitumor Agents, Kemal Sancak, Yasemi̇n Ünver, Mustafa Er
Turkish Journal of Chemistry
2-Amino-1,3,4-thiadiazoles compounds (2a-e) were obtained from the reaction of thiosemi carbazide with 2-cyanomethoxyphenoxyacetonitriles (1). Mono acylamino, mono aroylamino and diethoxycarbonyl imino-1,3,4-thiadiazole compounds (3a-e, 4a-e, 5a-c) were synthesized via the reaction of 2-amino-1,3,4-thiadiazole compounds (2a-e) with acetyl chloride or acetic anhydride, benzoyl chloride or benzoic anhydride and ethyl chloroformate, respectively. The in vitro antitumor activities of some selected compounds were screened and compounds 2a, 2b, 2c, 3a, 3b, 3c, 5a, 5b and 5c were found to be active.
Synthesis Of Some Novel 3,5-Diaryl-1,2,4-Triazole Derivatives And Investigation Of Their Antimicrobial Activities, Mevlut Serdar, Nurhan Gümrükçüoğlu, Şengül Alpay Karaoğlu, Nesli̇han Demi̇rbaş
Synthesis Of Some Novel 3,5-Diaryl-1,2,4-Triazole Derivatives And Investigation Of Their Antimicrobial Activities, Mevlut Serdar, Nurhan Gümrükçüoğlu, Şengül Alpay Karaoğlu, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
A series of acylhydrazones (2a-d) was synthesized from the reactions of iminoester hydrochlorides (1a-e) with acyl hydrazines. 2,5-Dialkyl 1,3,4-oxadiazoles (3a-d) were obtained in the same reaction media. The treatment of acylhydrazones with hydrazine hydrate afforded 4-amino-3,5-dialkyl-1,2,4-triazoles (4a-c). The acetylation of 4-amino-3-(4-hydroxyphenyl)-5-phenyl-4H-1,2,4-triazole (4a) produced 4-amino-5-(4-acetoxyphenyl)-3-phenyl-4H-1,2,4-triazole (9), while the acetylation of 4-amino-3-(4-tolyl)-5-phenyl-4H-1,2,4-triazole (4b) gave 4-acetylamino-3-phenyl-5-(4-tolyl)-4H-1,2,4-triazole (10). The treatment of compound 4b with various aromatic aldehydes or acetophenone and 4-nitroacetophenone resulted in the formation of 4-arylidenamino-3,5-dialkyl-4H-1,2,4-triazoles (5a-e and 7a,b). Sodium borohydride reduction of 4-arylidenamino derivatives of 1,2,4-triazoles afforded 4-alkylamino-3,5-dialkyl-4H-1,2,4-triazoles (6a-e and 8a,b). All newly synthesized compounds were screened for their antimicrobial and antifungal …
Synthesis And Antimicrobial Activities Of Some New 1,2,4-Triazole Derivatives, Nurhan Gümrükçüoğlu, Mevlut Serdar, Eli̇f Çeli̇k, Ali̇ Sevi̇m, Nesli̇han Demi̇rbaş
Synthesis And Antimicrobial Activities Of Some New 1,2,4-Triazole Derivatives, Nurhan Gümrükçüoğlu, Mevlut Serdar, Eli̇f Çeli̇k, Ali̇ Sevi̇m, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
A series of acylhydrazones (2a-f) were synthesized by the condensation of iminoester hydrochlorides (1a-f) with acyl hydrazines. 2,5-Dialkyl 1,3,4-oxadiazoles (3a,c,e) were obtained in the same reaction media. The treatment of acylhydrazones with hydrazine hydrate afforded 4-amino-3,5-dialkyl-1,2,4-triazoles (4a-c). The acetylation of 4-amino-3,5-dialkyl-1,2,4-triazoles produced N-[3,5-dialkyl-4H-1,2,4-triazol-4-yl] acetamides (5-7). The treatment of compounds 4a and 4c with various aromatic aldehydes resulted in the formation of 4-arylidenamino-3,5-dialkyl-1,2,4-triazoles (8a,d, e, and 10a-e). Sodium borohydride reduction of 4-arylidenamino derivatives afforded 4-alkylamino-3,5-dialkyl-1,2,4-triazoles (9a,d, e, and 11a-e). Compounds 4b, 4c, 7, 8d, and 11c showed good antifungal activity only against yeast-like fungi, while compounds 3e, 6, 8e, and 9e …