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Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Characterization Of Anderson-Evans Type Polyoxometalates, Antibacterial Properties, Hülya Avci Özbek
Synthesis And Characterization Of Anderson-Evans Type Polyoxometalates, Antibacterial Properties, Hülya Avci Özbek
Turkish Journal of Chemistry
In the present work, the new aluminium-substituted polyoxometalates of the Anderson-Evans type have been prepared and structurally defined by the reaction of aluminium (III) chloride hexahydrate and sodium tungstate dihydrate/sodium molybdate dihydrate in an aqueous basic medium. Elemental analysis, FT-IR, TGA, 1H NMR, and 31P NMR analysis revealed that these polyoxometalates had the following formula: [Ph4 P]3 [Al(OH)6 Mo6 O18]·4H2 O 1, [Ph4 P]3 [Al(OH)6 W6 O18]·4H2 O 2, [C7 H10N]3 [Al(OH)6 Mo6 O18]·4H2 O 3, [C7 H10N]3 [Al(OH)6 W6 O18]·4H2 O 4. The compounds 1 and 2 show promising antibacterial activity against gram-positive Staphylcoccus aureus ATCC 25923 and gram-negative …
Synthesis, Molecular Simulation Studies, In Vitro Biological Assessment Of 2-Substituted Benzoxazole Derivatives As Promising Antimicrobial Agents, Gajanan S. Shanbhan, Amit Bhargava, Giridhar Pal Singh, Shrinivas D. Joshi, Narendra Chundawat
Synthesis, Molecular Simulation Studies, In Vitro Biological Assessment Of 2-Substituted Benzoxazole Derivatives As Promising Antimicrobial Agents, Gajanan S. Shanbhan, Amit Bhargava, Giridhar Pal Singh, Shrinivas D. Joshi, Narendra Chundawat
Turkish Journal of Chemistry
The 2-substituted benzoxazole derivatives are known to exhibit a wide spectrum of biological potential. Two series of novel benzoxazole derivatives containing 2-phenyl and 2-N-phenyl groups were synthesized, by following the green chemistry approach. All the newly synthesized derivatives were screened against gram-positive bacteria (Streptococcus pyogenes, Staphylococcus aureus), gram-negative bacteria (Pseudomonas aeruginosa, Escherichia coli) and the fungus (Aspergillus clavatus and Candida albicans). Most of these compounds have demonstrated potent antibacterial activities, especially against E. coli at 25 μg/mL, along with moderate antifungal activity. Among these, two compounds, 21 and 18, showed interesting antibacterial profile. Molecular …
Major Chemical Constituents From Illicium Griffithii Hook. F. & Thoms Of North East India And Their Cytotoxicity And Antimicrobial Activities, Deepjyoti Dutta, Bardwi Narzary, Snigdha Saikia, Kashyap J. Tamuli, Manobjyoti Bordoloi, Neipihoi Lhouvum, Shyamalendu Nath, Ranjan K. Sahoo, Barnali Gogoi, Surovi Saikia, Nayan K. Bhattacharyya
Major Chemical Constituents From Illicium Griffithii Hook. F. & Thoms Of North East India And Their Cytotoxicity And Antimicrobial Activities, Deepjyoti Dutta, Bardwi Narzary, Snigdha Saikia, Kashyap J. Tamuli, Manobjyoti Bordoloi, Neipihoi Lhouvum, Shyamalendu Nath, Ranjan K. Sahoo, Barnali Gogoi, Surovi Saikia, Nayan K. Bhattacharyya
Turkish Journal of Chemistry
Illicium griffithii Hook. f. & Thoms is an endemic medicinal plant of North East India found in the Eastern Himalayan region of biodiversity mega centre. Herein, chemical investigation of I. griffithii, afforded five compounds and their structures were determined through extensive use of NMR, HRMS, and FT-IR spectroscopy. The complete proton-proton, proton-carbon coupling network of compound 1 was determined using 1H-1H COSY, HSQC and NOESY NMR experiments. All the compounds were evaluated for their cytotoxic activity by MTT assay and antimicrobial activity by Agar well diffusion method. Compound 1 exhibited significant cytotoxicity activity against Lung cancer (A549) and pancreatic …
Thio-Schiff Bases Derived From 2,2'-Disulfanedianiline Via Nanocerium Oxide: Antimicrobial Effect And Antiproliferative Effects In Melanoma Cells, Aslihan Dalmaz, Sefa Durmuş, Görkem Dülger, Merve Alpay
Thio-Schiff Bases Derived From 2,2'-Disulfanedianiline Via Nanocerium Oxide: Antimicrobial Effect And Antiproliferative Effects In Melanoma Cells, Aslihan Dalmaz, Sefa Durmuş, Görkem Dülger, Merve Alpay
Turkish Journal of Chemistry
In this study, the synthesis of dimeric disulfide-Schiff bases was carried out using two methods. The structures of the obtained Schiff bases were elucidated by various spectroscopic methods as well as elemental analysis. The Schiff base derivative compounds (3a-6) were screened for in vitro antibacterial activity against multidrug-resistant microorganisms using microdilution method. All the tested compounds showed varying inhibition zones against the pathogens. According to MIC results, the compound 2 was shown strong inhibitory activity against all the tested microorganisms compared to antibiotics. In addition, all the tested compounds showed different antiproliferative effects on the melanoma cell line (B16F10). Our …
Cyclotide-Rich Fractions Containing Nanofibers By Electrospinning: Preparation, Characterization And Examination Of Antimicrobial Activity, Eli̇f Büşra Baş, Cemi̇l Kürekci̇, Orhan Murat Kalfa, Muharrem Akcan
Cyclotide-Rich Fractions Containing Nanofibers By Electrospinning: Preparation, Characterization And Examination Of Antimicrobial Activity, Eli̇f Büşra Baş, Cemi̇l Kürekci̇, Orhan Murat Kalfa, Muharrem Akcan
Turkish Journal of Chemistry
In this study, antimicrobial nanofibers were produced with the mixtures of polyvinyl alcohol (PVA) and cyclotide-rich fractions by electrospinning method. After extraction, the first separation was carried out with C18 flash chromatography and then fractioned into five separate parts by reversed-phase high-pressure liquid chromatography (RP-HPLC). The molecular weights of cyclotides in each fraction were determined by quadrupole time-of-flight liquid chromatography-mass spectrometry (Q-TOF LC-MS). Cyclotide-rich fractions were mixed with 10% of PVA solution and nanofibers were produced from this biocomposite mixture by electrospinning method. The nanofibers were characterized by field emission scanning electron microscopy (FE-SEM), and it was observed that 100% …
Synthesis, Characterization, And Antimicrobial Evaluation Of Polyvinylalcohol-Osthol Composite Films, Ishrat Gowsia, Feroz Mir, Javid Banday
Synthesis, Characterization, And Antimicrobial Evaluation Of Polyvinylalcohol-Osthol Composite Films, Ishrat Gowsia, Feroz Mir, Javid Banday
Turkish Journal of Chemistry
Although poly-vinyl alcohol (PVA) has certain mechanical drawbacks such as a weak barrier, it has widely been used in food packaging over the last many years. To increase the suitability of PVA (C2H4O)n and render it ideal for food packaging, a diversity of studies have already been carried out. In the below-mentioned script, we, for the first time, report the use of natural product osthol in making a new composite with PVA for enhancing thermal, physicochemical, and antimicrobial properties. The significant aim of the report is the insertion of osthol (C15H16O3 …
Synthesis, Characterization, And Biological Evaluation Of New Copper Complexes Ofnaphthyl Pyrazole Ligands, Melek Hinis, Kuldip Singh, Demet Erdönmez, Ayfer Menteş
Synthesis, Characterization, And Biological Evaluation Of New Copper Complexes Ofnaphthyl Pyrazole Ligands, Melek Hinis, Kuldip Singh, Demet Erdönmez, Ayfer Menteş
Turkish Journal of Chemistry
Two naphthalene pyrazole ligands were synthesized using KOH/DMSO and Cu catalyst and characterized with FT-IR, ESIMS, 1H, and 13C NMR spectroscopies. The crystal structures of 1-(2-methylnaphthalen-1-yl)-1H-pyrazole (MeNap-Pz) ligand have been determined with X-ray crystal structure analysis. Reaction of the ligands with Cu(NO3)2x3.5H2O gave two new complexes and characterized with magnetic susceptibility, molar conductance, FT-IR, LCMS-MS, ICP-OES, NMR, thermogravimetric analysis, and ESR spectra. The spectral data of the ligands are coordinated to the metal ion through the nitrogen atoms of the pyrazole ring. Consequently, it has been determined that [Cu(MeNap-Pz)2 (NO3)]NO3.2H2O complex showed square planar geometry and [Cu(NapMe-Pz)2(NO3)2].H2O complex showed octahedral …
First Determination Of Some Phenolic Compounds And Antimicrobial Activities Ofgeranium Ibericum Subsp. Jubatum: A Plant Endemic To Turkey, Mehmet Emi̇n Şeker, Emri̇ye Ay, Ayça Aktaş Karaçeli̇k, Rena Hüseyi̇noğlu, Derya Efe
First Determination Of Some Phenolic Compounds And Antimicrobial Activities Ofgeranium Ibericum Subsp. Jubatum: A Plant Endemic To Turkey, Mehmet Emi̇n Şeker, Emri̇ye Ay, Ayça Aktaş Karaçeli̇k, Rena Hüseyi̇noğlu, Derya Efe
Turkish Journal of Chemistry
This paper includes the results of the first study about the phenolic characteristics and antimicrobial analyses of Geranium İbericum subsp. jubatum species found in Turkey. In the present work, the phenolic contents of different parts of the G. İbericum (flower, root, leaf ) were determined with high-performance liquid chromatography (HPLC)-DAD (diode-array detector) and liquid chromatography (LC)-MS/MS (mass spectrometry). The following phenolic compounds were investigated: catechin, protocatechuic acid, gallic acid, ellagic acid, chlorogenic acid, 4-hydroxybenzaldehyde, p-coumaric acid, rutin, naringenin, kaempferol. Based on the results obtained, the roots and flowers of the plant are found to be very rich in ellagic acid …
Syntheses And Antibacterial Activities Of 4 Linear Nonphenolic Diarylheptanoids, Şemsi̇ Betül Demi̇r, Hati̇ce Seçi̇nti̇, Nesli̇han Çelebi̇oğlu, Murat Özdal, Alev Sezen, Özlem Gülmez, Ömer Faruk Algur, Hasan Seçen
Syntheses And Antibacterial Activities Of 4 Linear Nonphenolic Diarylheptanoids, Şemsi̇ Betül Demi̇r, Hati̇ce Seçi̇nti̇, Nesli̇han Çelebi̇oğlu, Murat Özdal, Alev Sezen, Özlem Gülmez, Ömer Faruk Algur, Hasan Seçen
Turkish Journal of Chemistry
Four linear nonphenolic diarylheptanoids were synthesized and their antibacterial activities were studied. ($S)$-2-Me-CBS-catalysed reduction of alnustone with BH$_{3}$.SMe$_{2}$ gave ($R)$(-)(4$E$,6$E)$-1,7-diphenylhepta-4,6-dien-3-ol, a natural product. Reduction of alnustone with Na in t-BuOH at -15 $^{\circ}$C under NH$_{3}$ atm gave ($E)$-1,7-diphenylhept-5-en-3-one as a Birch-type reduction product. $t$-BuOK catalysed condensation of benzalacetone with propionyl chloride gave (4$Z$,6$E)$-5-hydroxy-1,7-diphenylhepta-4,6-dien-3-one, a natural product. (1$E$,4$Z$,6$E)$-5-Hydroxy-4-phenethyl-1,7-diphenylhepta-1,4,6-trien-3-one, a curcuminoid, was synthesized starting from pentan-2,4-dione in 3 steps. The synthesized chemical compounds were applied against 2 gram-positive bacteria (Bacillus cereus and Arthrobacter agilis), 4 gram-negative bacteria (Pseudomonas aeruginosa, Xanthomonas campestris, Klebsiella oxytoca and Helicobacter pylori), and 1 yeast (Candida albicans) by …
Synthesis And Spectroscopic Properties Of (N/O) Mono- Anddispirocyclotriphosphazene Derivatives With Benzyl Pendant Arms: Study Ofbiological Activity?, Özlem İşcan, Reşi̇t Cemaloğlu, Nuran Asmafi̇li̇z, Zeynel Kiliç, Leyla Açik, Peli̇n Özbeden, Tuncer Hökelek
Synthesis And Spectroscopic Properties Of (N/O) Mono- Anddispirocyclotriphosphazene Derivatives With Benzyl Pendant Arms: Study Ofbiological Activity?, Özlem İşcan, Reşi̇t Cemaloğlu, Nuran Asmafi̇li̇z, Zeynel Kiliç, Leyla Açik, Peli̇n Özbeden, Tuncer Hökelek
Turkish Journal of Chemistry
The Cl replacement reactions of hexachlorocyclotriphosphazene (trimer; N3 P3 Cl6) with sodium (N-benzyl)- aminopropanoxides (1 and 2) produced monospiro- (3 and 4), cis-, and trans-dispirocyclotriphosphazenes (13-16). The monospiro tetrakis-aminocyclotriphosphazenes (5-12) were obtained by the Cl substitutions of 3 and 4 with different secondary amines. The cis- (13 and 14) and trans-dispirophosphazenes (15 and 16) possessed 2 chiral P centers, and they were able to present meso and racemic forms, respectively. Moreover, the structures of compounds 5 and 14 were designated using X-ray data. The absolute configuration of compound 14 was found as SR in the solid state. Analytical and spectroscopic …
Synthesis Of $E$-Stilbene Azomethines As Potent Antimicrobial And Antioxidant Agents, Ahsan Iqbal, Zulfiqar Ali Khan, Sohail Anjum Shahzad, Muhammad Usman, Shakeel Ahmad Khan, Abdul H. Fauq, Ayesha Bari, Muhammad Aamir Sajid
Synthesis Of $E$-Stilbene Azomethines As Potent Antimicrobial And Antioxidant Agents, Ahsan Iqbal, Zulfiqar Ali Khan, Sohail Anjum Shahzad, Muhammad Usman, Shakeel Ahmad Khan, Abdul H. Fauq, Ayesha Bari, Muhammad Aamir Sajid
Turkish Journal of Chemistry
A series of new extensively conjugated $E$-stilbene azomethines (5a-5h) were synthesized and screened for their antioxidant and antimicrobial activity. The compounds were tested against bacterial (Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, and Bacillus subtilis) and fungal strains (Aspergillus niger, A. flavus, and Trichoderma harzianum) using the agar well diffusion method. Among the tested compounds, $N$'-(4-nitrobenzylidene)-2-(($E)$-styryl)benzohydrazide (5g) was found to possess potent antimicrobial activity higher than some drugs with significant activity reported in the literature, e.g., cefradine and terbinafine hydrochloride. Additionally, compounds 5a-5h were also evaluated for antioxidant potential using DPPH free radical scavenging and ferric thiocyanate (FTC) assays. Among these, …
Synthesis, Characterization, And Antimicrobial Activities Of Novel Monosaccharide-Containing Schiff Base Ligands, Fatma Telli̇, Stephen Thomas Astley, Azi̇ze Yeşi̇m Salman
Synthesis, Characterization, And Antimicrobial Activities Of Novel Monosaccharide-Containing Schiff Base Ligands, Fatma Telli̇, Stephen Thomas Astley, Azi̇ze Yeşi̇m Salman
Turkish Journal of Chemistry
Four new chiral Schiff base ligands (3a-4a, 3b-4b) have been prepared using aminoisopropylidene derivatives of glucose and aminochloralose derivatives of mannose. The synthesized compounds 1 and 2 were characterized by nuclear magnetic resonance ($^{1}$H and $^{13}$C NMR), Fourier transform infrared spectroscopy (FTIR), UV/visible spectroscopy, and elemental analysis. A total of eight Schiff base compounds (3a-6a, 3b-6b) were tested for antimicrobial activity against Escherichia coli ATCC 12228, Staphylococcus aureus ATCC 6538, Klebsiella pneumoniae CCM 2318, Pseudomonas aeruginosa ATCC 27853, Salmonella typhimurium CCM 5445, Enterococcus faecalis ATCC 29212, Bacillus subtilis ATCC 6633, and Candida albicans ATCC 10239 and exhibited a range of …
The Reactions Of N$_{3}$P$_{3}$Cl$_{6}$ With Monodentate And Bidentate Ligands: The Syntheses And Structural Characterizations, In Vitro Antimicrobial Activities, And Dna Interactions Of 4-Fluorobenzyl(N/O)Spirocyclotriphosphazenes, Aytuğ Okumuş, Gamze Elmas, Zeynel Kiliç, Nagehan Ramazanoğlu, Leyla Açik, Mustafa Türk, Gülçi̇n Akca
The Reactions Of N$_{3}$P$_{3}$Cl$_{6}$ With Monodentate And Bidentate Ligands: The Syntheses And Structural Characterizations, In Vitro Antimicrobial Activities, And Dna Interactions Of 4-Fluorobenzyl(N/O)Spirocyclotriphosphazenes, Aytuğ Okumuş, Gamze Elmas, Zeynel Kiliç, Nagehan Ramazanoğlu, Leyla Açik, Mustafa Türk, Gülçi̇n Akca
Turkish Journal of Chemistry
The Cl replacement reactions of 4-fluorobenzyl(N/O)spirocyclotriphosphazene (2) with excess monoamines led to the formation of 4-fluorobenzylspiro(N/O)tetraaminocyclotriphosphazenes (2a-2d). The partly substituted \textbf{dispiro 3b and dispiro 3c and fully substituted trispirocyclotriphosphazenes (trans 4a, cis 4c, 4d, and 4e) were obtained, respectively, from the reactions of 2 with one equimolar and two equimolar amounts of diamines, aminoalcohol, and diols. Although efforts were made for the separation of the cis/trans and optical isomers of the dispiro phosphazenes, only one set of diastereomers (RR/RS or SS/SR) of dispiro 3b and dispiro 3c was isolated, respectively. The $^{31}$P NMR spectral data of the other dispiro phosphazenes …
Synthesis, And Prediction Of Molecular Properties And Antimicrobial Activity Of Some Acylhydrazones Derived From $N$-(Arylsulfonyl)Methionine, Esra Tatar, Sevi̇l Şenkardeş, Hasan Erdi̇nç Selli̇tepe, Şükri̇ye Güni̇z Küçükgüzel, Şengül Alpay Karaoğlu, Ari̇f Bozdeveci̇, Erik De Clercq, Christophe Pannecouque, Tai̇bi̇ Ben Hadda, İlkay Küçükgüzel
Synthesis, And Prediction Of Molecular Properties And Antimicrobial Activity Of Some Acylhydrazones Derived From $N$-(Arylsulfonyl)Methionine, Esra Tatar, Sevi̇l Şenkardeş, Hasan Erdi̇nç Selli̇tepe, Şükri̇ye Güni̇z Küçükgüzel, Şengül Alpay Karaoğlu, Ari̇f Bozdeveci̇, Erik De Clercq, Christophe Pannecouque, Tai̇bi̇ Ben Hadda, İlkay Küçükgüzel
Turkish Journal of Chemistry
A series of 38 new acylhydrazones [3-40], derived from (2$S)$-4-(methylsulfanyl)-2-[[(4-methylphenyl)sulfonyl] amino]butanoic acid hydrazide [2], were synthesized and evaluated for their anti-HIV and antimicrobial activity with the further aim to develop acylhydrazones carrying an amino acid side chain. All tested compounds possess stronger activity against gram (+) bacteria. Compound 23 was found active against methicillin-resistant Staphylococcus aureus (MRSA) with a MIC value of 3.9 $\mu $g/mL. The MIC value of compound 30 against Enterococcus faecalis, Listeria monocytogenes, and Bacillus cereus was 8 $\mu $g/mL. A computational study for prediction of ADME and drug-like properties (solubility, drug-likeness, and drug score) as well …
Synthesis And Biological Evaluation Of A New Series Of 4-Alkoxy-2-Arylquinoline Derivatives As Potential Antituberculosis Agents, Gonca Tosun, Tayfun Arslan, Zeynep İskefi̇yeli̇, Murat Küçük, Şengül Alpay Karaoğlu, Nuretti̇n Yayli
Synthesis And Biological Evaluation Of A New Series Of 4-Alkoxy-2-Arylquinoline Derivatives As Potential Antituberculosis Agents, Gonca Tosun, Tayfun Arslan, Zeynep İskefi̇yeli̇, Murat Küçük, Şengül Alpay Karaoğlu, Nuretti̇n Yayli
Turkish Journal of Chemistry
Three new series of 33 quinolone compounds, 2-(2-, 3-, and 4-fluorophenyl)-4-O-alkyl(C$_{5-15})$quinolines (7a-k, 8a-k, and 9a-k), were synthesized from 2-(2-, 3-, and 4-fluorophenyl)-2,3-dihydroquinolin-4(1H)-one (4, 5, and 6) by the reaction of alkyl halides under basic conditions in DMF. The new compounds 7a-k, 8a-k, and 9a-k were synthesized from flavonones 4-6, which can be considered new precursors for quinoline synthesis through a one-step reaction. All the target compounds (7a-k, 8a-k, and 9a-k) were evaluated for their in vitro antimicrobial activity against nine test microorganisms. They showed the most activity against Mycobacterium smegmatis with minimum inhibitory concentrations (MIC) of 62.5-500 $\mu $g/mL, indicating …
A New Series Of Cu(Ii) And Ni(Ii) Complexes Of No Bidentate 4-No$_{2}$-Benzoylhydrazones: Synthesis, Characterization, And Biological Studies, Hati̇ce Başpinar Küçük, Emel Mataraci Kara, Berna Özbek Çeli̇k
A New Series Of Cu(Ii) And Ni(Ii) Complexes Of No Bidentate 4-No$_{2}$-Benzoylhydrazones: Synthesis, Characterization, And Biological Studies, Hati̇ce Başpinar Küçük, Emel Mataraci Kara, Berna Özbek Çeli̇k
Turkish Journal of Chemistry
A series of new nickel(II) and copper(II) hydrazone complexes \textbf{1--14}, containing a bidentate NO-donor hydrazone ligand, derived from 4-nitrobenzoylhydrazide and several aliphatic and aromatic aldehydes were synthesized, and their chemical structures were confirmed by means of FT-IR, UV-Vis, $^{1}$H and $^{13}$C NMR, mass spectral data, conductance measurements, and elemental analyses. The spectral data of the newly synthesized complexes show the formation of a 1:2 [metal:ligand] ratio. The ligands and their complexes were also investigated for their possible in vitro antimicrobial activities against \textit{S. aureus}, \textit{S. epidermidis}, \textit{E. coli}, \textit{K. pneumonia}, \textit{P. aeruginosa}, \textit{P. mirabilis}, \textit{E. faecalis}, and \textit{C. albicans}. Among …
Synthesis Of Tertiary Propargylic Phosphonates By Addition Of Trialkynylaluminum Reagents To Acyl Phosphonates And Investigation Of Their Antimicrobial Activities, Muhammed Shakhawoat Hossain, Sidika Polat Çakir, Ayşe Betül Karaduman, Mustafa Yamaç, Ayhan Sitki Demi̇r
Synthesis Of Tertiary Propargylic Phosphonates By Addition Of Trialkynylaluminum Reagents To Acyl Phosphonates And Investigation Of Their Antimicrobial Activities, Muhammed Shakhawoat Hossain, Sidika Polat Çakir, Ayşe Betül Karaduman, Mustafa Yamaç, Ayhan Sitki Demi̇r
Turkish Journal of Chemistry
A series of propargylic alcohols containing phosphonates was synthesized by addition reactions of tris-(propynyl) and tris-(phenylethynyl)aluminum reagents to acyl phosphonates in good yields. Aromatic moieties of the acyl phosphonates with electron-withdrawing groups generally resulted in better isolated chemical yield. Selected propargylic phosphonates were tested for antimicrobial activities. Compounds 3a and 3h showed noticeable antifungal activity, especially against molds.
Synthesis And Biological Activities Of Methylenebis-4h-1,2,4-Triazole Derivatives, Yildiz Uygun, Hacer Bayrak, Havva Özkan
Synthesis And Biological Activities Of Methylenebis-4h-1,2,4-Triazole Derivatives, Yildiz Uygun, Hacer Bayrak, Havva Özkan
Turkish Journal of Chemistry
5,5'-Methylenebis(4--phenyl-4H-1,2,4-triazole-3-thiol) (2) was synthesized starting from hydrazinecarbothioamide compound (1). Treatment of compound 2 with ethyl bromoacetate produced diethyl 5,5'-{methylenebis[(4-phenyl-4H-1,2,4-triazole-5,3-diyl)thio]}diacetate (3), which was converted to the corresponding diacetohydrazide derivative (4) by treatment with hydrazine hydrate. The reaction of compound 4 with several aldehydes produced the corresponding arylidene hydrazides, 5a--d. Syntheses of Mannich bases 6a--c were carried out by the treatment of compound 2 with several amines in the presence of formaldehyde. (4{[5-({5-[(4-Amino-2-chlorophenyl)thio]-4-phenyl-4H-1,2,4-triazol-3-ylmethyl)-4-phenyl-4H-1,2,4-triazol-3-yl]thio}-3-chlorophenyl)amine (8) was prepared by reduction of 2 nitro groups of 3,3' -methylenebis{5-[(2-chloro-4-nitrophenyl)thio]-4-phenyl-4H-1,2,4-triazole} (7) that were obtained from the condensation of 2} with 3,4-dichloronitrobenzene. The newly synthesized compounds were screened …
Synthesis And Antimicrobial Investigation Of Some 5h-Pyridazino[4,5-B]Indoles, İlker Avan, Alaetti̇n Güven, Kiymet Güven
Synthesis And Antimicrobial Investigation Of Some 5h-Pyridazino[4,5-B]Indoles, İlker Avan, Alaetti̇n Güven, Kiymet Güven
Turkish Journal of Chemistry
Synthesis and in vitro antimicrobial activities are reported for a series of 1,3,5-substituted 4-oxo-3,4-dihydro-5H-pyridazino[4,5-b]indole derivatives. Corresponding pyridazino[4,5-b]indoles were prepared from ethyl 3-formyl-1H-indole-2-carboxylate precursors and the functional group in question was installed with hydrazine and its derivatives. The purity and primary structures of pyridazino[4,5-b]indole were confirmed by IR, ^1 H NMR, and ^{13}C NMR spectroscopy and elemental analyses. All of the indoles were tested for in vitro antimicrobial activity against 8 isolates of bacteria and a fungus including Staphylococcus aureus NRRL B-767, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Proteus vulgaris NRRL-B123, Salmonella typhimurium NRRL B-4420, Bacillus subtilis NRRL 744, …
N-Functionalized Benzimidazol-2-Ylidene Silver Complexes: Synthesis, Characterization, And Antimicrobial Studies, Yetki̇n Gök, Senem Akkoç, Özlem Özeroğlu Çeli̇kal, İlknur Özdemi̇r, Selami̇ Günal, Eli̇f Sayin
N-Functionalized Benzimidazol-2-Ylidene Silver Complexes: Synthesis, Characterization, And Antimicrobial Studies, Yetki̇n Gök, Senem Akkoç, Özlem Özeroğlu Çeli̇kal, İlknur Özdemi̇r, Selami̇ Günal, Eli̇f Sayin
Turkish Journal of Chemistry
2-Methoxyethyl, 2-diethylaminoethyl, and 2-phenylethyl-substituted N-heterocyclic carbene (NHC) precursors were treated with Ag_2CO_3 to yield silver(I)-NHC complexes (1a--g) in dichloromethane as a solvent at room temperature. The 7 new silver-NHC complexes were fully characterized by means of ^1H NMR, ^{13}C NMR, and elemental analysis techniques. Using the agar dilution procedure recommended by the Laboratory and Clinical Standards Institute, the antimicrobial activities of all the silver-NHC complexes were studied against 2 gram-negative bacterial strains (Pseudomonas aeruginosa and Escherichia coli), 2 gram-positive bacterial strains (Enterococcus faecalis and Staphylococcus aureus), and 2 fungi (Candida tropicalis and Candida albicans).
Synthesis Of Linezolid-Like Molecules And Evaluation Of Their Antimicrobial Activities, Serap Başoğlu, Meltem Yolal, Ahmet Demi̇rbaş, Hakan Bektaş, Rza Abbasoğlu, Nesli̇han Demi̇rbaş
Synthesis Of Linezolid-Like Molecules And Evaluation Of Their Antimicrobial Activities, Serap Başoğlu, Meltem Yolal, Ahmet Demi̇rbaş, Hakan Bektaş, Rza Abbasoğlu, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
3-Fluoro-4-(morpholin-4-yl)aniline (2), prepared from 3,4-difluoronitrobenzene, was converted to the corresponding Schiff base (3) by treatment with indol-3-carbaldehyde. The treatment of thiourea 4 and carbothioamide derivatives 9 with ethyl bromoacetate or 4-substituted phenacyl bromides generated the corresponding thiazolidinone (5 and 13) and thiazoline (6 and 12) derivatives, respectively. The acidic or basic treatment of carbothioamide 9 produced 1,3,4-thiadiazole (11) or 1,2,4-triazole (10) compounds, respectively. The structural assignments of the new compounds were based on elemental analysis and spectral (IR, ^1H-NMR, ^{13}C-NMR, and LC-MS) data. The antimicrobial activity study revealed that all compounds showed good antitubercular activities.
Synthesis, Characterization, And Antimicrobial Activity Of A New Pyrimidine Schiff Base And Its Cu(Ii), Ni(Ii), Co(Ii), Pt(Ii), And Pd(Ii) Complexes, Mehmet Gülcan, Mehmet Sönmez, İsmet Berber
Synthesis, Characterization, And Antimicrobial Activity Of A New Pyrimidine Schiff Base And Its Cu(Ii), Ni(Ii), Co(Ii), Pt(Ii), And Pd(Ii) Complexes, Mehmet Gülcan, Mehmet Sönmez, İsmet Berber
Turkish Journal of Chemistry
A new Schiff base, {1-[(5-bromo-2-hydroxy-benzylidene)- amino]-4-phenyl-2-thioxo-1,2-dihyro-pyrimidin-5-yl}-phenyl-methanone, was synthesized from N-amino pyrimidine-2-thione and 5-bromsalicylaldehyde. Metal complexes of the Schiff base were prepared from acetate salts of Cu(II), Ni(II), Co(II), Pd(II), and PtCl_2 in methanol. The chemical structures of the Schiff base ligand and its metal complexes were confirmed by spectroscopic analysis. All of the compounds were evaluated for their antimicrobial against 4 gram-positive bacteria, 1 gram-negative bacterium, and 3 yeast strains. The Schiff base and the Cu(II) and Co(II) complexes showed good biological activity against all tested bacteria and yeast strains.
Preparation And Antimicrobial Activity Evaluation Of Some Quinoline Derivatives Containing An Azole Nucleus, Muhammet Özyanik, Serpi̇l Demi̇rci̇, Hakan Bektaş, Nesli̇han Demi̇rbaş, Ahmet Demi̇rbaş, Şengül Alpay Karaoğlu
Preparation And Antimicrobial Activity Evaluation Of Some Quinoline Derivatives Containing An Azole Nucleus, Muhammet Özyanik, Serpi̇l Demi̇rci̇, Hakan Bektaş, Nesli̇han Demi̇rbaş, Ahmet Demi̇rbaş, Şengül Alpay Karaoğlu
Turkish Journal of Chemistry
Quinoline-2-carbohydrazide (2) obtained from quinaldic acid (1) was converted to the corresponding carbothioamide 3 and carboxamide 6 by treatment with benzyliso(thio)cyanate. The basic treatment of 3 and 6 yielded the corresponding 1,2,4-triazole derivatives 4 and 7. The synthesis of 5-(quinolin-2-yl)-1,3,4- oxadiazol-2-thiol (9) was performed from the reaction of 1 with CS_2 in basic media. The Mannich reaction of compounds 4, 7, and 9 resulted in the formation of aminoalkylated derivatives 5a-c, 8, and 10a,b. The condensation of 1 with thiosemicarbazide, carbohydrazide, or thiocarbohydrazide gave the corresponding 1,2,4-triazole derivatives (11-13). The treatment of 4-amino-5-(quinolin-2-yl)- 4H-1,2,4-triazole-3-thiol (13) with 4-chlorophenacyl bromide caused the …
Novel Biologically Active Glycosides From The Aerial Parts Of Cephalaria Gazipashensis, Nazli Böke Sarikahya, Süheyla Kirmizigül
Novel Biologically Active Glycosides From The Aerial Parts Of Cephalaria Gazipashensis, Nazli Böke Sarikahya, Süheyla Kirmizigül
Turkish Journal of Chemistry
Two new triterpene glycosides, 3-O-\beta-D-glucopyranosyl- (1\to 4)-\beta-D-xylopyranosyl-(1\to 3)-\alpha-L-rhamnopyranosyl- (1\to 3)-\alpha-L-arabinopyranosyl olean-12-ene 28-O-\beta -D- glucopyranosyl-(1\to 6)-\beta-D-glucopyranosyl ester (gazipashoside A, 1) and 3-O-\beta-D-glucopyranosyl-(1\to 4)-\beta-D-xylopyranosyl- (1\to 3)-\alpha-L-rhamnopyranosyl-(1\to 2)-\alpha-L-arabinopyranosyl hederagenin 28-O-\beta -D-glucopyranosyl-(1\to 6)-\beta-D-glucopyranosyl ester (gazipashoside B, 2), were isolated together with 11 known compounds including 7 triterpene, 1 flavonoid, and 3 iridoidal metabolites from the aerial parts of Cephalaria gazipashensis (Dipsacaceae). The structures of all compounds were elucidated by extensive evaluation of the spectroscopic data (1D- and 2D- NMR, HRESI-MS), as well as chemical examinations. The antimicrobial effects of all pure compounds were tested against gram-positive and gram-negative bacteria. The results indicated that the …
Synthesis And Antimicrobial Evaluation Of Some Annelated Phthalazine Derivatives And Acyclo C-Nucleosides From 1-Chloro-4-(2,4,6-Trimethylphenyl) Phthalazine Precursor, Maher Abdel Aziz El-Hashash, Ahmed Youssef Soliman, Ibrahim Essam Elshamy
Synthesis And Antimicrobial Evaluation Of Some Annelated Phthalazine Derivatives And Acyclo C-Nucleosides From 1-Chloro-4-(2,4,6-Trimethylphenyl) Phthalazine Precursor, Maher Abdel Aziz El-Hashash, Ahmed Youssef Soliman, Ibrahim Essam Elshamy
Turkish Journal of Chemistry
A highly efficient and versatile synthetic approach to the synthesis of annelated phthalazine derivatives viz. 1,2,4-triazolo [3,4-a]phthalazine 11a,b, 14, 18, 19a,b, 29-31, 33, 1,2,4-triazino [3,4-a]phthalazine 25a,b-28, 1,3,5-triazino[4,3-a]phthalazine 22, tetrazolo[5,1-a] phthalazine 23, imidazophthalazine 9a,b,15, and pyrimidinophthlazine 6, 10, 16, 17, 20 is presented. Moreover, acyclo C-nucleoside and double headed acyclo C-nucleoside of 1,2,4-triazolo[3,4-a]phthalazine 12, 13 were obtained via heterocyclization reaction of 1-chloro-4-(2,4,6-trimethylphenyl) phthalazine (4) with gluconic acid hydrazide and galactaric acid bis hydrazide, respectively. The new compounds were synthesized with the objective of studying their antimicrobial activity.
Design And Synthesis Of New 1,2,4-Triazole Derivatives Containing Morpholine Moiety As Antimicrobial Agents, Deni̇z Şahi̇n, Hacer Bayrak, Ahmet Demi̇rbaş, Nesli̇han Demi̇rbaş, Şengül Alpay Karaoğlu
Design And Synthesis Of New 1,2,4-Triazole Derivatives Containing Morpholine Moiety As Antimicrobial Agents, Deni̇z Şahi̇n, Hacer Bayrak, Ahmet Demi̇rbaş, Nesli̇han Demi̇rbaş, Şengül Alpay Karaoğlu
Turkish Journal of Chemistry
2-Morpholine-4ylethyl-3H-1,2,4-triazole-3-ones (2a, 2b) were obtained from the condensation between the corresponding ethoxycarbonylhydrazones and 2-morpholinoethanamine. 2a was converted to acetohydrazide (4) via the formation of an ester derivative (3). Treatment of 2a and 2b with several aryl sulfonyl chlorides afforded the corresponding 2-arylsulfonyl-1,2,4-triazole-3-ones (5a-c and 6). The reaction of hydrazide (4) with benzyl iso- and benzyl isothiocyanate produced the corresponding carboxamide (8a) and carbothioamide (8b). The basic treatment of 8b yielded 5-mercapto-4H-1,2,4-triazol-3-yl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one (10). The synthesis of 1,3-thiazol-2(3H)-ylidene-1,2,4-triazol-1- ylacetohydrazide (11) and 1,3-oxazole-2(3H)-ylidene-1,2,4-triazole- 1-yl)acetohydrazide (9) derivatives was performed from the reaction of 8a and 8b with substituted phenacyl bromides. All the newly synthesized …
Reduction, Mannich Reaction And Antimicrobial Activity Evaluation Of Some New 1,2,4-Triazol-3-One Derivatives, Seda Fandakli, Serap Başoğlu, Hakan Bektaş, Meltem Yolal, Ahmet Demi̇rbaş, Şengül Alpay Karaoğlu
Reduction, Mannich Reaction And Antimicrobial Activity Evaluation Of Some New 1,2,4-Triazol-3-One Derivatives, Seda Fandakli, Serap Başoğlu, Hakan Bektaş, Meltem Yolal, Ahmet Demi̇rbaş, Şengül Alpay Karaoğlu
Turkish Journal of Chemistry
Ethyl[4-arylmethyleneamino-3-(4-metylphenyl)-5-oxo-4,5-dihydro- 1H-1,2,4-triazole-1-yl]acetates (3a-e and 10a-d) were obtained starting from 4-amino-2,4-dihydro-3H-1,2,4-triazol-3-ones (1 and 9) in 2 steps. The treatment of 3a-e with NaBH_4 resulted in the formation of 3 kinds of product incorporating carboxcilic acid (4a-c) or alcohol (5a-e) functionality. [4-{[(4-Methoxyphenyl)methylene]amino}- and 4-{[pyridin-4-ylmethylene]amino}-3-(4-methylphenyl)-5-oxo-4,5-dihydro-1H- 1,2,4-triazole-1-yl] acetic acids (6a, 6e) were obtained by the hydrolysis of the corresponding esters (5a-5e). The treatment of 6a with NaBH_4 caused the reduction of only the imine bond; the carboxyl group remained unchanged. Then this carboxylic acid was converted to the corresponding hydrazide (8) in 2 steps by reaction with ethanol and hydrazine hydrate, respectively. The synthesis …
Synthesis And Antioxidant And Antimicrobial Evaluation Of Novel 4-Substituted-1h-1,2,4-Triazole Derivatives, Sultan Baytaş, Evi̇n Kapçak, Tülay Çoban, Hati̇ce Özbi̇lge
Synthesis And Antioxidant And Antimicrobial Evaluation Of Novel 4-Substituted-1h-1,2,4-Triazole Derivatives, Sultan Baytaş, Evi̇n Kapçak, Tülay Çoban, Hati̇ce Özbi̇lge
Turkish Journal of Chemistry
A series of 4-benzyl/phenyl-3-(1-methyl-1H-indole-2-yl)-1H- 1,2,4-triazole-5(4H)-thione (4a,b) and 2-{4-[benzyl/phenyl-5- (substitutedbenzylthio)]-4H-1,2,4-triazole-3-yl}-1-methyl-1H-indole derivatives (5a-p) were synthesized and evaluated for their in vitro scavenging of DPPH and superoxide radical, and lipid peroxidation inhibition effects as well as their antimicrobial properties. DPPH radical scavenging capacity was found to be equipotent with BHT and found in compounds containing 1,2,4-triazole-5(4H)-thione moiety (4a,b). With regard to antimicrobial properties, compound 5k showed slight antimicrobial activity against all the test microorganisms.
Chemical Composition And Antimicrobial Activity Of The Essential Oils Of Geranium Columbinum L. And G. Lucidum L. (Geraniaceae), Niko Radulovic, Milan Dekic, Zorica Stojanovic-Radic, Radosav Palic
Chemical Composition And Antimicrobial Activity Of The Essential Oils Of Geranium Columbinum L. And G. Lucidum L. (Geraniaceae), Niko Radulovic, Milan Dekic, Zorica Stojanovic-Radic, Radosav Palic
Turkish Journal of Chemistry
The chemistry of Geranium columbinum and G. lucidum volatiles has been studied here for the first time. The essential oils were obtained by hydrodistillation, analyzed by GC and GC-MS, and screened for their in vitro antibacterial and antifungal activity in a microdilution assay. In total, 172 constituents were identified, accounting for 88.1%-96.7% of the detected GC peak areas. The essential oils consisted mainly of fatty acids and fatty acid-derived compounds (65.0%-86.3%). The major compounds of the essential oils were hexadecanoic acid, hexahydrofarnesyl acetone, and tetracosane. The antimicrobial assay showed a strong activity of the oil from aerial parts of G. …
Synthesis And Antimicrobial Activity Of Novel 2-(Pyridin-2-Yl)Thieno[2,3-D]Pyrimidin-4 (3h)-Ones, Nitin G. Haswani, Sanjaykumar B. Bari
Synthesis And Antimicrobial Activity Of Novel 2-(Pyridin-2-Yl)Thieno[2,3-D]Pyrimidin-4 (3h)-Ones, Nitin G. Haswani, Sanjaykumar B. Bari
Turkish Journal of Chemistry
In the present study, some new 2-(pyridin-2-yl)thieno[2,3-d] pyrimidin-4(3H)-ones derivatives (IIa-o) were synthesized. The target compounds (IIa-o) were synthesized through the acid catalyzed condensation of 2-cyano, 3-cyano, and 4-cyano-pyridines with various 2-amino-3-carbethoxythiophenes (Ia-e). All thiophene derivatives were synthesized by Gewald reaction. The structures of the newly synthesized compounds were confirmed by UV-Visible, FT-IR, ^1H-NMR, and mass spectral studies. All synthesized compounds were evaluated for their antimicrobial activity against various gram-positive and gram-negative bacterial and fungal strains. Amongst the synthesized compounds IIa, IIb, IId, IIe, and IIm were found to be active.