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Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Biological Evaluation Of Novel Fused Triazolo[4,3-$A$] Pyrimidinones, Ikhlass Abbas, Sobhi Gomha, Mohamed Elneairy, Mahmoud Elaasser, Bazada Mabrouk
Synthesis And Biological Evaluation Of Novel Fused Triazolo[4,3-$A$] Pyrimidinones, Ikhlass Abbas, Sobhi Gomha, Mohamed Elneairy, Mahmoud Elaasser, Bazada Mabrouk
Turkish Journal of Chemistry
The reaction of thione 3 or its 2-methylthio derivative 4 with hydrazonoyl halides 5a-l, in the presence of triethylamine, yielded the corresponding triazolo[4,3-$a$]pyrimidin-5(1$H)$-ones 8a-l. The structure of compounds 8a-l was further confirmed by the reaction of 3 with the appropriate active chloromethylenes 11a-c followed by coupling of the products with benzenediazonium chloride to afford the azo-coupling products 6b, f, and j, which were converted in situ to 8b, f, and j. 2-Hydrazinyl-pyrido[3',2':4,5]thieno[3,2-$d$]pyrimidin-4(3$H)$-one (13) was prepared and condensed with different aldehydes 14a-f to give the corresponding hydrazone derivatives 15a-f. Oxidative cyclization of the hydrazones 15a-f give the corresponding triazolo[4,3-$a$] pyrimidin-5(1$H)$-one derivatives …
Synthesis And Biological Evaluation Of New Pyridines Containing Imidazole Moiety As Antimicrobial And Anticancer Agents, Ikhlass Abbas, Sobhi Gomha, Mahmoud Elaasser, Mohammed Bauomi
Synthesis And Biological Evaluation Of New Pyridines Containing Imidazole Moiety As Antimicrobial And Anticancer Agents, Ikhlass Abbas, Sobhi Gomha, Mahmoud Elaasser, Mohammed Bauomi
Turkish Journal of Chemistry
The synthesis of a novel series of pyridine and bipyridine derivatives is described via one-pot multicomponent reaction of 5-acetylimidazole, malonitrile (or ethylcyanoacetate or diethylmalonate), substituted benzaldehyde (or terephthaldehyde), and ammonium acetate in good yields. The structures of all the new compounds were elucidated on the basis of elemental analysis and spectral data. The antimicrobial activities of the synthesized compounds were screened and the results showed that most of such compounds exhibit considerable activities. Furthermore, some of the newly synthesized compounds were screened for their anticancer activity against human breast cell line (MCF-7) and liver carcinoma cell line (HEPG2) in comparison …
Two New Coordination Polymers Containing Dicyanidoargentate(I) And Dicyanidoaurate(I): Synthesis And Characterization, And A Detailed In Vitro Investigation Of Their Anticancer Activities On Some Cancer Cell Lines, Ali̇ Aydin, Ahmet Karadağ, Şaban Teki̇n, Nesri̇n Korkmaz, Aslihan Özdemi̇r
Two New Coordination Polymers Containing Dicyanidoargentate(I) And Dicyanidoaurate(I): Synthesis And Characterization, And A Detailed In Vitro Investigation Of Their Anticancer Activities On Some Cancer Cell Lines, Ali̇ Aydin, Ahmet Karadağ, Şaban Teki̇n, Nesri̇n Korkmaz, Aslihan Özdemi̇r
Turkish Journal of Chemistry
Two novel cyanido-bridged bimetallic polymeric complexes, [Ni(edbea)Ag$_{3}$(CN)$_{5}$]$_{n} $(C1) and [Ni(bishydeten) Au$_{2}$(CN)$_{4}$]$_{n}$ (C2), where edbea = [2,2$' $-(ethylenedioxy)bis(ethylamine)] and bishydeten = [($N$,$N' $-bis(2-hydroxyethyl) ethylenediamine)] are ligands, were synthesized and characterized by elemental, infrared, and thermal measurement techniques and investigated for their biological activity in cultured cancer cell lines. The results show that both compounds and free anions, [Ag(CN)$_{2}$]$^{-}$ and [Au(CN)$_{2}$]$^{-}$, exhibited very high antiproliferative activity compared to the anticancer drug 5FU against the cancer cell lines tested. The antiproliferative and cytotoxic activities of C1 and C2 were significantly lower than those of free anions, indicating that the extreme cytotoxicity of free …
Synthesis Of Novel 1,2,4-Triazoles And Triazolo-Thiadiazines As Anticancer Agents, Thoraya Abd El-Reheem Farghaly, Magda Ahmad Abdallah, Huda Kamel Mmahmoud
Synthesis Of Novel 1,2,4-Triazoles And Triazolo-Thiadiazines As Anticancer Agents, Thoraya Abd El-Reheem Farghaly, Magda Ahmad Abdallah, Huda Kamel Mmahmoud
Turkish Journal of Chemistry
A new series of 7-arylazo-5$H$-3-(trifluoromethyl)-6-methyl-1,2,4-triazolo-[3,4-$b$]-1,3,4-thiadiazines was prepared by reaction of 4-amino-3-trifluoromethyl-5-mercapto-1,2,4-triazoles with $N$-aryl-2-oxo-propane hydrazonoyl chloride in dioxane under reflux in the presence of triethylamine. Furthermore, Schiff bases of 4-amino-5-mercapto-1,2,4-triazole derivatives were reacted with a variety of hydrazonoyl chlorides and gave the respective hydrazonothioates. In addition, the novel \textit{bis}-(1,2,4-triazole-3-thione) was reacted with the appropriate hydrazonoyl chloride in dioxane under reflux in the presence of triethylamine to give the corresponding \textit{bis}-(1,2,4-triazolethiohydrazonoate). The structures of the new compounds were established based on elemental and spectral data. The mechanism of the studied reaction was also discussed. Moreover, some of the new products were screened …