Research Article
BibTex RIS Cite

HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI

Year 2018, Volume: 13 Issue: 2, 24 - 30, 22.04.2018

Hafize Telçeken Arzu Karatepe Mehmet Ataş , Taner Daştan Mustafa Karatepe

Abstract

Schiff bazları epoksidasyon reaksiyonlarında
katalizör, iletken polimerlerin eldesinde monomer, antifungal, antibakteriyel, antimikrobiyal
ve bazı oksidatif radikal türlerine karşı antioksidan olarak kullanılmaktadır. Son
yılllarda, birçok Schiff bazları türevi sentezlenmeye devam edilmektedir. Bu araştırmada,
hidroksiüre türevi Schiff bazı Cu (L-Cu), Cd (L-Cd) ve Zn (L-Zn) metal komplekslerinin
antimikrobiyal aktiviteleri in vitro olarak
araştırıldı. In vitro denemelerde mikrodilüsyon
broth metodu uygulandı.  Sonuç olarak in vitro çalışmada
Hidroksiüre Schiff bazı metal kompleksleri etkili bir antimikrobiyal aktivite göstermiştir.

Keywords

Hidroksiüre Schiff Bazı Metal Kompleksi Antimikrobiyal Polimer

References

  • [1] Durackova, Z., Mendiola, M.A., Sevilla, M.T., and Valent, A., (1999). Thiohydrazone Copper (II) Complexes. The Relationship Between Redox Properties and Superoxide Dismutase Mimetic Activity. Bioelectrochemistry and Bioenergetics: 48, 109-116.
  • [2] Liberta, A.E. and West, D.X., (1992). Antifungal and Antitumour Activity of Heterocyclic Thiosemicarbazones and Their Metal Complexes. Biometals: 5, 121-126.
  • [3] Fioravanti, R., Biava, M., Donnarumma, S., Porretta G.C., Simonetti, N., Villa, A., Porta-Puglia, A., Deiddo, D., Maullo, C., and Pompei, R., (1996). Synthesis and Microbiological Evaluations of (N-heteroaryl) Arylmethanamines and Their Schiff Bases. IL Far: 51, 643-652.
  • [4] Yang, Z.Y., Yang, R.D., Li, F.S., and Yu, K.B., (2000). Crystal Structure and Antitumor Activity of some Rare Earth Metal Complexes With SchiffBase. Polyhedron: 19, 2599-2604.
  • [5] Das, A., Trousdale, M.D., Ren, S., and Lien, E.J., (1999). Inhibition of Herpes Simplex Virus Type 1 and Adenovirus Type 5 by Heterocyclic Schiff Bases of Aminohydroxyguanidine Tosylate. Antiviral Research: 44, 201-208.
  • [6] Sur, B., Chatterjee, S.P., Sur, P., Maity, T., and Roychoudhury, S., (1990). Studies on the Antineoplasticity of Schiff Bases Containing 5-nitrofuran and Pyrimidine. Oncology: 47, 433-438.
  • [7] Pires dos Santos, M.L., Alairo, A.F., Mangrich, A.S., and Ferreira, A.M.C., (1998). Antioxidant and Pro-oxidant Properties of some di-Schiff Base copper(II) Complexes. J. of Inorg. Biochem: 71,71-78.
  • [8] Cory, J.G., Cory, A.H., Rappa, G., Lorico, A., Liu, M.C., Lin, T.S., and Sartorelli, A.C., (1995). Structure-function Relationships for a New Series of Pyridine-2-carboxaldehyde Thiosemicarbazones on Ribonucleotide Reductase Activity and Tumor Cell Growth in Culture and in Vivo: Adv. Enz. Regul:35, 55-68.
  • [9] Cory, J.G., Carter, G.L., Bacon, P.E., Tang, A., and Lien, E.J., (1985). Inhibition of Ribonucleotide Reductase and L1210 Cell Growth by N-hydroxy-N'-aminoguanidine Derivatives. Biochem. Pharmacol:34, 2645-2650.
  • [10] Huili, C. and Chang, T.C., (1990). Studies on the Thermotropic Liquid Crystalline Polymer. Journal of Polymer Science: Part A: Polymer Chemistry: 28, 3625-3638.
  • [11] Huili, C. and Chang, T.C., (1991). Studies on the Thermotropic Liquid Crystalline Polymer. Eur. Polym. J.:27, 35-39.
  • [12] Gaber, M. and Issa, R.M., (1989). Studies of Ti(IV) and Zr(IV) Chelates with N2O2; Schiff Bases of 2-hydroxy-1-naphthaldehyde with Aromatic Diamines. Therm. Acta:155, 309-316.
  • [13] Reddy, K.H. and Lingappa, Y., (1994). Synthesis and Characterization of Copper (ii) Complexes of Physiologically Active Tridentate Schiff-Bases. Indian J. of Chemistry: 33, 919-923.
  • [14] Kuduk, J., (1994). New Platinium (II) Complexes with Schiff Base Ligands. Tran. Met. Chem: 19, 296-298.
  • [15] Chen, D., Martell, A.E., and Sun, Y., (1989). New Synthetic Cobalt Schiff Base Complexes as Oxygen Carriers. Inorg. Chem:28, 2647-2652.
  • [16] Isse, A.A., Gennaro, A., and Vianello, E., (1991). Electrochemical Reduction of Carbon Dioxide Catalyzed by [CoI(salophen)Li]. J. Mol. Catal:70, 197-208.
  • [17] Felicio, R.C., Cavalheiro, E.T.G., and Dockal, E.R., (2001). Preparation, Characterization and Thermogravimetric Studies of [N,N′-cis-1,2-cyclohexylenebis(salicylideneaminato)]cobalt(II)and[N,N′-(±)-trans-1,2-cyclo-hexylene bis(salicylideneaminato)]cobalt(II). Polyhedron: 20, 261-268.
  • [18] Eichhorn, E., Reicker, A., Speiser, B., and Stahl, H., (1997). Electrochemistry of Oxygenation Catalysts. 3.(1) Thermodynamic Characterization of Electron Transfer and Solvent Exchange Reactions of Co(salen)/[Co(salen)](+) in DMF, Pyridine, and Their Mixtures. Inorg. Chem: 36, 3307-3317.
  • [19] Salman, S.R., Farrant, R.D., and Lindon, J.C., (1991). Studies of Tautomerism in 2-Hydroxynaphthaldehyde Schiff Bases by Multinuclear Magnetic Resonance. Spect. Letters: An International Journal for Rapid Communication: 24, 1071-1078.
  • [20] Xu, D., Chen, B., Chen K., Chen C., Miki, K., and Kasai, N., (1989). The Molecular Structure of a Schiff Base Complex,[N,N′-Ethylenebis(1-phenyl-2-mino1butanonato)] acetonitrile) manganese(III) Perchlorate. Bull. Chem. Soc. Jpn: 62, 2384-2386.
  • [21] Wu, Z.Y., Xu, D.J., and Feng, Z.X., (2001). Synthesis and Catalytic Properties of a Ni(II) complex with tetraglycol aldehyde bis(methionine) Schiff base. Polyhedron: 20, 281-284.
  • [22] Eloff, J.N. (1998). A Sensitive and Quick Microplate Method to Determine the Minimal İnhibitory Concentration of Plant Extracts for Bacteria. Planta Med: 64, 711–713.
  • [23] CLSI, (2012). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, Approved Standard, 9th ed., CLSI document M07-A9. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA.
  • [24] CLSI, (2002). Reference Method for Broth Dilution Antifungal Suscept- ibility Testing of Yeasts, Approved Standard, 2nd ed., NCCLS document M27- A2. CLSI, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087- 1898, USA.
  • [25] Adiguzel, R., Esener, H., Ergin, Z., Aktan, E., Turan, N., and Sekerci, M., (2011). Synthesis and Characterization of Novel Ni(II), Cu(II) and Cd(II) Complexes of 4-(2-clorphenylazo)-1hpyrazole-3,5-diamine. Asian J Chem: 23, 1846-1850.
  • [26] Esener, H. Adiguzel, R. Ergin, Z. Aktan, E. Turan, N. and Sekerci, M., (2011). Synthesis and Characterization of Novel Mn(II), Co(III), Ni(II) and Cd(II) Complexes from 4-(2-nitrophenylazo)-1H-pryazole-3,5diamine. Advanced Sci Let: 4, 3669-3675.
  • [27] Kuete, V., (2010). Potential of Cameroonian Plants and Derived Products Against Microbial İnfections: A Review. Planta Med. 76 1479–1491.
  • [28] Awouafack, M.D., McGaw, L.J., Gottfried, S., Mbouangouere R., Tane, P., Spiteller, M., and Eloff, J.N. (2013). Antimicrobial Activity and Cytotoxicity of the Ethanol Extract, Fractions and Eight Compounds Isolated from Eriosema Robustum (Faba-ceae). BMC Complementary and Alternative Medicine, 13, 289. https://doi.org/10.1186/1472-6882-13-289.
  • [29] Liberta, A.E. and West, D.X. (1992). Antifungal and Antitumour Activity of Heterocyclic Thiosemicarbazones and Their Metal Complexes. Biometals: 5, 121–126.
  • [30] Tantaru, G. Poita, A. Bibire, N. (2017). Synthesis and Biological Evaluation of a New Schiff Bases and Its Cu (II) Complex. Revista de Chimie: 68(3), 586-588.
  • [31] Mohamed, G.G., (2006). Synthesis, Characterization and Biological Activity of Bis(phenylimine) Schiff Base Ligands and Their Metal Complexes. Spect. Acta: Mol. and Biomol. Spect.:64, 188-195.
  • [32] Rudzinski, W.E., Aminabhavi, T.M., Birada, N.S., and Patil, C.S., (1982). Biologically Active Sulfonamide Schiff Base Complexes of Selenium (IV) and Tellurium (IV). Inorg. Chim. Acta:67, 177-182.
  • [33] Telçeken, H., (2017). Hidroksiüre Türevi Schiff Bazı Metal Komplekslerinin in Vivo ve in Vitro Antitümör Özelliklerinin Araştırılması. Yüksek Lisans Tezi.
  • [34] Keypour, H., Mahmoudabadi, M., and e.g., (2018). Cadmium (II) Macrocyclic Schiff-base Complexes Containing Piperazine Moiety: Synthesis, Spectroscopic, X-ray Structure, Theoretical and Antibacterial Studies. J. Of Mol. Structure:1155, 196-204.
  • [35] Liu, J., Qu, W., and Kadiiska, M.B., (2009). Role of Oxidative Stress in Cadmium Toxicity and Carcinogenesis. Toxicology and Applied Pharmacology:238, 209–214.

Year 2018, Volume: 13 Issue: 2, 24 - 30, 22.04.2018

Hafize Telçeken Arzu Karatepe Mehmet Ataş , Taner Daştan Mustafa Karatepe

Abstract

References

  • [1] Durackova, Z., Mendiola, M.A., Sevilla, M.T., and Valent, A., (1999). Thiohydrazone Copper (II) Complexes. The Relationship Between Redox Properties and Superoxide Dismutase Mimetic Activity. Bioelectrochemistry and Bioenergetics: 48, 109-116.
  • [2] Liberta, A.E. and West, D.X., (1992). Antifungal and Antitumour Activity of Heterocyclic Thiosemicarbazones and Their Metal Complexes. Biometals: 5, 121-126.
  • [3] Fioravanti, R., Biava, M., Donnarumma, S., Porretta G.C., Simonetti, N., Villa, A., Porta-Puglia, A., Deiddo, D., Maullo, C., and Pompei, R., (1996). Synthesis and Microbiological Evaluations of (N-heteroaryl) Arylmethanamines and Their Schiff Bases. IL Far: 51, 643-652.
  • [4] Yang, Z.Y., Yang, R.D., Li, F.S., and Yu, K.B., (2000). Crystal Structure and Antitumor Activity of some Rare Earth Metal Complexes With SchiffBase. Polyhedron: 19, 2599-2604.
  • [5] Das, A., Trousdale, M.D., Ren, S., and Lien, E.J., (1999). Inhibition of Herpes Simplex Virus Type 1 and Adenovirus Type 5 by Heterocyclic Schiff Bases of Aminohydroxyguanidine Tosylate. Antiviral Research: 44, 201-208.
  • [6] Sur, B., Chatterjee, S.P., Sur, P., Maity, T., and Roychoudhury, S., (1990). Studies on the Antineoplasticity of Schiff Bases Containing 5-nitrofuran and Pyrimidine. Oncology: 47, 433-438.
  • [7] Pires dos Santos, M.L., Alairo, A.F., Mangrich, A.S., and Ferreira, A.M.C., (1998). Antioxidant and Pro-oxidant Properties of some di-Schiff Base copper(II) Complexes. J. of Inorg. Biochem: 71,71-78.
  • [8] Cory, J.G., Cory, A.H., Rappa, G., Lorico, A., Liu, M.C., Lin, T.S., and Sartorelli, A.C., (1995). Structure-function Relationships for a New Series of Pyridine-2-carboxaldehyde Thiosemicarbazones on Ribonucleotide Reductase Activity and Tumor Cell Growth in Culture and in Vivo: Adv. Enz. Regul:35, 55-68.
  • [9] Cory, J.G., Carter, G.L., Bacon, P.E., Tang, A., and Lien, E.J., (1985). Inhibition of Ribonucleotide Reductase and L1210 Cell Growth by N-hydroxy-N'-aminoguanidine Derivatives. Biochem. Pharmacol:34, 2645-2650.
  • [10] Huili, C. and Chang, T.C., (1990). Studies on the Thermotropic Liquid Crystalline Polymer. Journal of Polymer Science: Part A: Polymer Chemistry: 28, 3625-3638.
  • [11] Huili, C. and Chang, T.C., (1991). Studies on the Thermotropic Liquid Crystalline Polymer. Eur. Polym. J.:27, 35-39.
  • [12] Gaber, M. and Issa, R.M., (1989). Studies of Ti(IV) and Zr(IV) Chelates with N2O2; Schiff Bases of 2-hydroxy-1-naphthaldehyde with Aromatic Diamines. Therm. Acta:155, 309-316.
  • [13] Reddy, K.H. and Lingappa, Y., (1994). Synthesis and Characterization of Copper (ii) Complexes of Physiologically Active Tridentate Schiff-Bases. Indian J. of Chemistry: 33, 919-923.
  • [14] Kuduk, J., (1994). New Platinium (II) Complexes with Schiff Base Ligands. Tran. Met. Chem: 19, 296-298.
  • [15] Chen, D., Martell, A.E., and Sun, Y., (1989). New Synthetic Cobalt Schiff Base Complexes as Oxygen Carriers. Inorg. Chem:28, 2647-2652.
  • [16] Isse, A.A., Gennaro, A., and Vianello, E., (1991). Electrochemical Reduction of Carbon Dioxide Catalyzed by [CoI(salophen)Li]. J. Mol. Catal:70, 197-208.
  • [17] Felicio, R.C., Cavalheiro, E.T.G., and Dockal, E.R., (2001). Preparation, Characterization and Thermogravimetric Studies of [N,N′-cis-1,2-cyclohexylenebis(salicylideneaminato)]cobalt(II)and[N,N′-(±)-trans-1,2-cyclo-hexylene bis(salicylideneaminato)]cobalt(II). Polyhedron: 20, 261-268.
  • [18] Eichhorn, E., Reicker, A., Speiser, B., and Stahl, H., (1997). Electrochemistry of Oxygenation Catalysts. 3.(1) Thermodynamic Characterization of Electron Transfer and Solvent Exchange Reactions of Co(salen)/[Co(salen)](+) in DMF, Pyridine, and Their Mixtures. Inorg. Chem: 36, 3307-3317.
  • [19] Salman, S.R., Farrant, R.D., and Lindon, J.C., (1991). Studies of Tautomerism in 2-Hydroxynaphthaldehyde Schiff Bases by Multinuclear Magnetic Resonance. Spect. Letters: An International Journal for Rapid Communication: 24, 1071-1078.
  • [20] Xu, D., Chen, B., Chen K., Chen C., Miki, K., and Kasai, N., (1989). The Molecular Structure of a Schiff Base Complex,[N,N′-Ethylenebis(1-phenyl-2-mino1butanonato)] acetonitrile) manganese(III) Perchlorate. Bull. Chem. Soc. Jpn: 62, 2384-2386.
  • [21] Wu, Z.Y., Xu, D.J., and Feng, Z.X., (2001). Synthesis and Catalytic Properties of a Ni(II) complex with tetraglycol aldehyde bis(methionine) Schiff base. Polyhedron: 20, 281-284.
  • [22] Eloff, J.N. (1998). A Sensitive and Quick Microplate Method to Determine the Minimal İnhibitory Concentration of Plant Extracts for Bacteria. Planta Med: 64, 711–713.
  • [23] CLSI, (2012). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, Approved Standard, 9th ed., CLSI document M07-A9. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA.
  • [24] CLSI, (2002). Reference Method for Broth Dilution Antifungal Suscept- ibility Testing of Yeasts, Approved Standard, 2nd ed., NCCLS document M27- A2. CLSI, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087- 1898, USA.
  • [25] Adiguzel, R., Esener, H., Ergin, Z., Aktan, E., Turan, N., and Sekerci, M., (2011). Synthesis and Characterization of Novel Ni(II), Cu(II) and Cd(II) Complexes of 4-(2-clorphenylazo)-1hpyrazole-3,5-diamine. Asian J Chem: 23, 1846-1850.
  • [26] Esener, H. Adiguzel, R. Ergin, Z. Aktan, E. Turan, N. and Sekerci, M., (2011). Synthesis and Characterization of Novel Mn(II), Co(III), Ni(II) and Cd(II) Complexes from 4-(2-nitrophenylazo)-1H-pryazole-3,5diamine. Advanced Sci Let: 4, 3669-3675.
  • [27] Kuete, V., (2010). Potential of Cameroonian Plants and Derived Products Against Microbial İnfections: A Review. Planta Med. 76 1479–1491.
  • [28] Awouafack, M.D., McGaw, L.J., Gottfried, S., Mbouangouere R., Tane, P., Spiteller, M., and Eloff, J.N. (2013). Antimicrobial Activity and Cytotoxicity of the Ethanol Extract, Fractions and Eight Compounds Isolated from Eriosema Robustum (Faba-ceae). BMC Complementary and Alternative Medicine, 13, 289. https://doi.org/10.1186/1472-6882-13-289.
  • [29] Liberta, A.E. and West, D.X. (1992). Antifungal and Antitumour Activity of Heterocyclic Thiosemicarbazones and Their Metal Complexes. Biometals: 5, 121–126.
  • [30] Tantaru, G. Poita, A. Bibire, N. (2017). Synthesis and Biological Evaluation of a New Schiff Bases and Its Cu (II) Complex. Revista de Chimie: 68(3), 586-588.
  • [31] Mohamed, G.G., (2006). Synthesis, Characterization and Biological Activity of Bis(phenylimine) Schiff Base Ligands and Their Metal Complexes. Spect. Acta: Mol. and Biomol. Spect.:64, 188-195.
  • [32] Rudzinski, W.E., Aminabhavi, T.M., Birada, N.S., and Patil, C.S., (1982). Biologically Active Sulfonamide Schiff Base Complexes of Selenium (IV) and Tellurium (IV). Inorg. Chim. Acta:67, 177-182.
  • [33] Telçeken, H., (2017). Hidroksiüre Türevi Schiff Bazı Metal Komplekslerinin in Vivo ve in Vitro Antitümör Özelliklerinin Araştırılması. Yüksek Lisans Tezi.
  • [34] Keypour, H., Mahmoudabadi, M., and e.g., (2018). Cadmium (II) Macrocyclic Schiff-base Complexes Containing Piperazine Moiety: Synthesis, Spectroscopic, X-ray Structure, Theoretical and Antibacterial Studies. J. Of Mol. Structure:1155, 196-204.
  • [35] Liu, J., Qu, W., and Kadiiska, M.B., (2009). Role of Oxidative Stress in Cadmium Toxicity and Carcinogenesis. Toxicology and Applied Pharmacology:238, 209–214.
There are 35 citations in total.

Details

Primary Language Turkish
Subjects Engineering
Journal Section Chemistry
Authors

Hafize Telçeken This is me

Arzu Karatepe This is me

Mehmet Ataş

Taner Daştan This is me

Mustafa Karatepe

Publication Date April 22, 2018
Published in Issue Year 2018 Volume: 13 Issue: 2

Cite

APA Telçeken, H., Karatepe, A., Ataş, M., Daştan, T., et al. (2018). HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI. Physical Sciences, 13(2), 24-30.
AMA Telçeken H, Karatepe A, Ataş M, Daştan T, Karatepe M. HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI. Physical Sciences. April 2018;13(2):24-30.
Chicago Telçeken, Hafize, Arzu Karatepe, Mehmet Ataş, Taner Daştan, and Mustafa Karatepe. “HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI”. Physical Sciences 13, no. 2 (April 2018): 24-30.
EndNote Telçeken H, Karatepe A, Ataş M, Daştan T, Karatepe M (April 1, 2018) HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI. Physical Sciences 13 2 24–30.
IEEE H. Telçeken, A. Karatepe, M. Ataş, T. Daştan, and M. Karatepe, “HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI”, Physical Sciences, vol. 13, no. 2, pp. 24–30, 2018.
ISNAD Telçeken, Hafize et al. “HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI”. Physical Sciences 13/2 (April 2018), 24-30.
JAMA Telçeken H, Karatepe A, Ataş M, Daştan T, Karatepe M. HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI. Physical Sciences. 2018;13:24–30.
MLA Telçeken, Hafize et al. “HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI”. Physical Sciences, vol. 13, no. 2, 2018, pp. 24-30.
Vancouver Telçeken H, Karatepe A, Ataş M, Daştan T, Karatepe M. HİDROKSİÜRE TÜREVİ SCHİFF BAZI METAL KOMPLEKSLERİNİN ANTİMİKROBİYAL ÖZELLİKLERİNİN ARAŞTIRILMASI. Physical Sciences. 2018;13(2):24-30.