Investigation of the Antimicrobial Activities of Schiff Bases Containing Triazoles
Year 2025,
Volume: 11 Issue: 1, 30 - 43, 28.02.2025
Hande Memiş
,
Şahin Direkel
,
Yasemin Ünver
,
Emel Uzunoğlu
,
Ülkü Karaman
,
Cihangir Akdemir
Abstract
Objective: Pathogen parasites and bacteria are microorganisms that have existed throughout human history and cause different diseases. Various antimicrobial agents have become one of the treatment options in the fight against these diseases. With the increase in the number of resistant microorganisms, existing agents became ineffective and there was a need to synthesize or produce new antibiotics, antiparasitic, antiviral and antifungal drugs. There are many studies showing that Schiff base derivatives have antimicrobial properties and proving the existence of their biological activities. In this study, it was aimed to determine the antimicrobial activity of two originally synthesized compounds, a triazole-containing Schiff base, against 16 different bacterial isolates and one different Leishmania species.
Methods: In our study, the biological activities of two different newly synthesized triazole-containing Schiff base derivatives against selected one Leishmania and 16 bacteria species were evaluated by the microdilution broth (alamar blue added) method. In the study, the in vitro antibacterial activities of the compounds were determined by measuring their Minimum Inhibitory Concentration (MIC) values.
Results: Leishmanicidal activity of Leishmania infantum parasite was determined by measuring its Leishmanicidal Concentration. The compounds were found to have antimicrobial activity against bacteria and parasite at different concentrations.
Conclusion: It was concluded that the in vitro antimicrobial activity results obtained in our study will be of significant benefit to future research due to the resistance detected against drugs used in the treatment of infectious diseases and health problems arising due to the side effects of the drugs. If in vivo animal experiments and toxicity studies are as expected; We believe that the in vitro antimicrobial activity results obtained in our study will make a significant contribution to future research due to the resistance detected against drugs used in the treatment of infectious diseases and the health problems caused by their side effects.
Supporting Institution
Giresun Üniversitesi Bilimsel Araştırma Projeleri Birimi tarafından SAĞ-BAP-A-270220-01 numaralı proje ile desteklenmiştir.
References
- Iscan D. Resistance Mechanism in Bacteria Against Various Antibiotics and Chemotherapeutics. Etlik Journal of Veterinary Microbiology. 1992;7(3):77-108.
- Iscan D. Resistance Mechanism in Bacteria Against Various Antibiotics and Chemotherapeutics. Etlik Journal of Veterinary Microbiology. 1992;7(3):77-108.
- Durger B, Ceyhan M, Alitsaous M, Ugurlu E. Antimicrobial Activity of Artemisia Absinthium L. (Wormwood). J. Of Biology. 1999;23: 377-384.
- Durger B, Ceyhan M, Alitsaous M, Ugurlu E. Antimicrobial Activity of Artemisia Absinthium L. (Wormwood). J. Of Biology. 1999;23: 377-384.
- Schwing A, Pomares C, Majoor A, Boyer L, Marty P, Michel G. Leishmania İnfection: Misdiagnosis As Cancer And Tumor-Promoting Potential. Acta Trop. 2019;197:104855.
- Schwing A, Pomares C, Majoor A, Boyer L, Marty P, Michel G. Leishmania İnfection: Misdiagnosis As Cancer And Tumor-Promoting Potential. Acta Trop. 2019;197:104855.
- Afroze A, Vinay P, Shailendra K, Kamlesh K, Naik MR. Anti-Leishmanial Activity Of Flavanone Analogues Targeting Pteridine Reductase, Indian Journal Of Pharmaceutical Education And Research. 2018;52(3):480-491.
- Afroze A, Vinay P, Shailendra K, Kamlesh K, Naik MR. Anti-Leishmanial Activity Of Flavanone Analogues Targeting Pteridine Reductase, Indian Journal Of Pharmaceutical Education And Research. 2018;52(3):480-491.
- Borghi SM, Fattori V, Costa IC, Filho PP, Pavanelli1 WR, Verri WR. Leishmania infection: Painful or Painless? Parasitol Res 2017;116:465–475 Doı 10.1007/S00436-016-5340-7.
- Borghi SM, Fattori V, Costa IC, Filho PP, Pavanelli1 WR, Verri WR. Leishmania infection: Painful or Painless? Parasitol Res 2017;116:465–475 Doı 10.1007/S00436-016-5340-7.
- Desjeux P. Worldwide increasing risk factors for leishmaniasis. Med. Microbiol. Immunol. 2001;190:77-79.
- Desjeux P. Worldwide increasing risk factors for leishmaniasis. Med. Microbiol. Immunol. 2001;190:77-79.
- Unver Y, Sancak K, Tanak H, Degirmencioglu İ, Dugdu E, Er M, et al. 5-Benzyl-4-[3-(1H-imidazol-1-yl)propyl]- 2H-1,2,4-triazol-3(4H)-ones: Synthesis, spectroscopic characterization, crystal structure and a comparison of theoretical and experimental IR results by DFT calculations. J.Mol. Struct. 2009;936,46-55.
- Unver Y, Sancak K, Tanak H, Degirmencioglu İ, Dugdu E, Er M, et al. 5-Benzyl-4-[3-(1H-imidazol-1-yl)propyl]- 2H-1,2,4-triazol-3(4H)-ones: Synthesis, spectroscopic characterization, crystal structure and a comparison of theoretical and experimental IR results by DFT calculations. J.Mol. Struct. 2009;936,46-55.
- Unver Y, Deniz S, Celik F, Akar Z, Kucuk M, Sancak K. Synthesis Of New 1,2,4-Triazole Compounds Containing Schiff And Mannich Bases (Morpholine) with Antioxidant And Antimicrobial Activities. Journal Of Enzym Inhibition and Medicinal Chemistry. 2016;31(3):89-95.
- Unver Y, Deniz S, Celik F, Akar Z, Kucuk M, Sancak K. Synthesis Of New 1,2,4-Triazole Compounds Containing Schiff And Mannich Bases (Morpholine) with Antioxidant And Antimicrobial Activities. Journal Of Enzym Inhibition and Medicinal Chemistry. 2016;31(3):89-95.
- Unver Y, Sancak K, Celik F, Birinci E, Kucuk M, Soylu S, et al. New Thiophene-1,2,4-Triazole-5(3)-Ones: Highly Bioactive Thiosemicarbazides, Structures Of Schiff Bases And Triazole-Thiols, European Journal Of Medicinal Chemistry. 2014;84 639-650.
- Unver Y, Sancak K, Celik F, Birinci E, Kucuk M, Soylu S, et al. New Thiophene-1,2,4-Triazole-5(3)-Ones: Highly Bioactive Thiosemicarbazides, Structures Of Schiff Bases And Triazole-Thiols, European Journal Of Medicinal Chemistry. 2014;84 639-650.
- Suleymanoglu N, Ustabas R, Direkel S, Bingöl Alpaslan Y, Unver Y. 1,2,4- Triazole Derivatives With Morpholine; Dft Study And Antileishmanial Activity. Canadian Journal Of Physics, 2018;96(7):719-723.
- Suleymanoglu N, Ustabas R, Direkel S, Bingöl Alpaslan Y, Unver Y. 1,2,4- Triazole Derivatives With Morpholine; Dft Study And Antileishmanial Activity. Canadian Journal Of Physics, 2018;96(7):719-723.
- Ikizler AA, Ucar F, Yuskek H, Aytin A, Yasa I, Gezer T. Synthesis and antifungal activity of some new arylidenamino compounds. Acta Pol Pharm, 1997; 54(2), 135-140).
- Ikizler AA, Ucar F, Yuskek H, Aytin A, Yasa I, Gezer T. Synthesis and antifungal activity of some new arylidenamino compounds. Acta Pol Pharm, 1997; 54(2), 135-140).
- Sumrra SH, Zafar W, Imran M, Chohan ZH. A review on the biomedical efficacy of transition metal triazole compounds. Journal of Coordination Chemistry. 2022;75(3-4): 293–334. DOI: 10.1080/00958972.2022.2059359
- Sumrra SH, Zafar W, Imran M, Chohan ZH. A review on the biomedical efficacy of transition metal triazole compounds. Journal of Coordination Chemistry. 2022;75(3-4): 293–334. DOI: 10.1080/00958972.2022.2059359
- Sancak B. Staphylococcus aureus And Antibiotic Resistance. Mikrobiyol Bul, 2011; 45(3):565-576.
- Sancak B. Staphylococcus aureus And Antibiotic Resistance. Mikrobiyol Bul, 2011; 45(3):565-576.
- Gazi H, Kurutepe S, Surucuoglu S, Ecemis T, Özbakkaloglu B. Antimicrobial Resistance in Hospital-Acquired Enterococcus Faecalis and Enterococcus Faecium Strains. Ankem Dergisi, 2004;18(1):49-52.
- Gazi H, Kurutepe S, Surucuoglu S, Ecemis T, Özbakkaloglu B. Antimicrobial Resistance in Hospital-Acquired Enterococcus Faecalis and Enterococcus Faecium Strains. Ankem Dergisi, 2004;18(1):49-52.
- Savasan S, Kaya O, Kirkan S, Ciftci A. Antibiotic resistance of fish-derived Enterococcus faecalis strains. Journal of Ankara University Faculty of Veterinary Medicine, 2008;55(2):107-110.
- Savasan S, Kaya O, Kirkan S, Ciftci A. Antibiotic resistance of fish-derived Enterococcus faecalis strains. Journal of Ankara University Faculty of Veterinary Medicine, 2008;55(2):107-110.
- Ciftci İH, Asık G. Antibiotic Resistance Mechanisms of Acinetobacter baumannii. Ankem Derg. 2011;25(3), 196-207.
- Ciftci İH, Asık G. Antibiotic Resistance Mechanisms of Acinetobacter baumannii. Ankem Derg. 2011;25(3), 196-207.
- Benkli K. Synthesis of Some 3-Arylamino-5-Aryloxymethyl [1, 2, 4] Triazole Derivatives and Investigation of their Antimicrobial Effects. Eskisehir: Anadolu University Health Sciences Institute. 2000.
- Benkli K. Synthesis of Some 3-Arylamino-5-Aryloxymethyl [1, 2, 4] Triazole Derivatives and Investigation of their Antimicrobial Effects. Eskisehir: Anadolu University Health Sciences Institute. 2000.
- Ozkanlı F, Dalkara S, Yulug N. Antibacterial and Antifungal Effect Studies on Some 2-Acetonaphtone and P-Chloroacetophenone Derivatives. Fabad J. Pharm. Sci, 1991;16:17-22.
- Ozkanlı F, Dalkara S, Yulug N. Antibacterial and Antifungal Effect Studies on Some 2-Acetonaphtone and P-Chloroacetophenone Derivatives. Fabad J. Pharm. Sci, 1991;16:17-22.
- Kocak G, Akdemir E. Anticancer, Apoptotic and Antibacterial Effects of Thiosemicarbazide and Bis-1, 2, 4-Triazole Derivatives. Bitlis Eren University Journal of Science. 2020;9(3):1124-1133.
- Kocak G, Akdemir E. Anticancer, Apoptotic and Antibacterial Effects of Thiosemicarbazide and Bis-1, 2, 4-Triazole Derivatives. Bitlis Eren University Journal of Science. 2020;9(3):1124-1133.
- Login CC, Bâldea I, Tiperciuc B, Benedec D, Vodnar DC, Decea N, et al. Thiazolyl Schiff Base: Antibacterial and Antifungal Effects and In Vitro Oxidative Stress Modulation on Human Endothelial Cells. Oxid Med Cell Longev. 2019; Volume 2019, Article ID 1607903, doi: 10.1155/2019/1607903.
- Login CC, Bâldea I, Tiperciuc B, Benedec D, Vodnar DC, Decea N, et al. Thiazolyl Schiff Base: Antibacterial and Antifungal Effects and In Vitro Oxidative Stress Modulation on Human Endothelial Cells. Oxid Med Cell Longev. 2019; Volume 2019, Article ID 1607903, doi: 10.1155/2019/1607903.
- Chohan ZH, Hanif M. Antibacterial and antifungal metal based triazole Schiff bases. J Enzyme Inhib Med Chem. 2023;(5):944-53. doi: 10.3109/14756366.2012.696246.
- Chohan ZH, Hanif M. Antibacterial and antifungal metal based triazole Schiff bases. J Enzyme Inhib Med Chem. 2023;(5):944-53. doi: 10.3109/14756366.2012.696246.
- Strzelecka M, Świątek P. 1,2,4-Triazoles as Important Antibacterial Agents. Pharmaceuticals (Basel). 2021;14(3):224. doi: 10.3390/ph14030224.
- Strzelecka M, Świątek P. 1,2,4-Triazoles as Important Antibacterial Agents. Pharmaceuticals (Basel). 2021;14(3):224. doi: 10.3390/ph14030224.
- Holanda VN, Silva WVD, Nascimento PHD, Silva SRB, Cabral Filho PE, Assis SPO, et al. Antileishmanial activity of 4-phenyl-1-[2-(phthalimido-2-yl)ethyl]-1H-1,2,3-triazole (PT4) derivative on Leishmania amazonensis and Leishmania braziliensis: In silico ADMET, in vitro activity, docking and molecular dynamic simulations. Bioorg Chem. 2020; 105:104437. doi: 10.1016/j.bioorg.104437.
- Holanda VN, Silva WVD, Nascimento PHD, Silva SRB, Cabral Filho PE, Assis SPO, et al. Antileishmanial activity of 4-phenyl-1-[2-(phthalimido-2-yl)ethyl]-1H-1,2,3-triazole (PT4) derivative on Leishmania amazonensis and Leishmania braziliensis: In silico ADMET, in vitro activity, docking and molecular dynamic simulations. Bioorg Chem. 2020; 105:104437. doi: 10.1016/j.bioorg.104437.
- Meinel RS, Almeida ADC, Stroppa PHF, Glanzmann N, Coimbra ES, da Silva AD. Novel functionalized 1,2,3-triazole derivatives exhibit antileishmanial activity, increase in total and mitochondrial-ROS and depolarization of mitochondrial membrane potential of Leishmania amazonensis. Chem Biol Interact. 2020;315:108850. doi: 10.1016/j.cbi.
- Meinel RS, Almeida ADC, Stroppa PHF, Glanzmann N, Coimbra ES, da Silva AD. Novel functionalized 1,2,3-triazole derivatives exhibit antileishmanial activity, increase in total and mitochondrial-ROS and depolarization of mitochondrial membrane potential of Leishmania amazonensis. Chem Biol Interact. 2020;315:108850. doi: 10.1016/j.cbi.
- das Chagas Almeida A, Meinel RS, Leal YL, Silva T P, Glanzmann N, Mendonca D V C, et al. Functionalized 1,2,3-triazolium salts as potential agents against visceral leishmaniasis. Parasitol Res. 2022;121(5):1389-1406. doi:10.1007/s00436-022-07431-9.
- das Chagas Almeida A, Meinel RS, Leal YL, Silva T P, Glanzmann N, Mendonca D V C, et al. Functionalized 1,2,3-triazolium salts as potential agents against visceral leishmaniasis. Parasitol Res. 2022;121(5):1389-1406. doi:10.1007/s00436-022-07431-9.
- Suleymanoglu N, Unver Y, Ustabas R, Direkel S, Alpaslan G. Antileishmanial activity study and theoretical calculations for 4-amino-1, 2, 4-triazole derivatives. Journal of Molecular Structure. 2017;1144:80-86
- Suleymanoglu N, Unver Y, Ustabas R, Direkel S, Alpaslan G. Antileishmanial activity study and theoretical calculations for 4-amino-1, 2, 4-triazole derivatives. Journal of Molecular Structure. 2017;1144:80-86
- Chen Y, Li P, Su S, Chen M, He J, Liu L, et al. Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base. RSC Adv. 2019;9(40):23045-23052. doi: 10.1039/c9ra05139b.
- Chen Y, Li P, Su S, Chen M, He J, Liu L, et al. Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base. RSC Adv. 2019;9(40):23045-23052. doi: 10.1039/c9ra05139b.
Year 2025,
Volume: 11 Issue: 1, 30 - 43, 28.02.2025
Hande Memiş
,
Şahin Direkel
,
Yasemin Ünver
,
Emel Uzunoğlu
,
Ülkü Karaman
,
Cihangir Akdemir
References
- Iscan D. Resistance Mechanism in Bacteria Against Various Antibiotics and Chemotherapeutics. Etlik Journal of Veterinary Microbiology. 1992;7(3):77-108.
- Iscan D. Resistance Mechanism in Bacteria Against Various Antibiotics and Chemotherapeutics. Etlik Journal of Veterinary Microbiology. 1992;7(3):77-108.
- Durger B, Ceyhan M, Alitsaous M, Ugurlu E. Antimicrobial Activity of Artemisia Absinthium L. (Wormwood). J. Of Biology. 1999;23: 377-384.
- Durger B, Ceyhan M, Alitsaous M, Ugurlu E. Antimicrobial Activity of Artemisia Absinthium L. (Wormwood). J. Of Biology. 1999;23: 377-384.
- Schwing A, Pomares C, Majoor A, Boyer L, Marty P, Michel G. Leishmania İnfection: Misdiagnosis As Cancer And Tumor-Promoting Potential. Acta Trop. 2019;197:104855.
- Schwing A, Pomares C, Majoor A, Boyer L, Marty P, Michel G. Leishmania İnfection: Misdiagnosis As Cancer And Tumor-Promoting Potential. Acta Trop. 2019;197:104855.
- Afroze A, Vinay P, Shailendra K, Kamlesh K, Naik MR. Anti-Leishmanial Activity Of Flavanone Analogues Targeting Pteridine Reductase, Indian Journal Of Pharmaceutical Education And Research. 2018;52(3):480-491.
- Afroze A, Vinay P, Shailendra K, Kamlesh K, Naik MR. Anti-Leishmanial Activity Of Flavanone Analogues Targeting Pteridine Reductase, Indian Journal Of Pharmaceutical Education And Research. 2018;52(3):480-491.
- Borghi SM, Fattori V, Costa IC, Filho PP, Pavanelli1 WR, Verri WR. Leishmania infection: Painful or Painless? Parasitol Res 2017;116:465–475 Doı 10.1007/S00436-016-5340-7.
- Borghi SM, Fattori V, Costa IC, Filho PP, Pavanelli1 WR, Verri WR. Leishmania infection: Painful or Painless? Parasitol Res 2017;116:465–475 Doı 10.1007/S00436-016-5340-7.
- Desjeux P. Worldwide increasing risk factors for leishmaniasis. Med. Microbiol. Immunol. 2001;190:77-79.
- Desjeux P. Worldwide increasing risk factors for leishmaniasis. Med. Microbiol. Immunol. 2001;190:77-79.
- Unver Y, Sancak K, Tanak H, Degirmencioglu İ, Dugdu E, Er M, et al. 5-Benzyl-4-[3-(1H-imidazol-1-yl)propyl]- 2H-1,2,4-triazol-3(4H)-ones: Synthesis, spectroscopic characterization, crystal structure and a comparison of theoretical and experimental IR results by DFT calculations. J.Mol. Struct. 2009;936,46-55.
- Unver Y, Sancak K, Tanak H, Degirmencioglu İ, Dugdu E, Er M, et al. 5-Benzyl-4-[3-(1H-imidazol-1-yl)propyl]- 2H-1,2,4-triazol-3(4H)-ones: Synthesis, spectroscopic characterization, crystal structure and a comparison of theoretical and experimental IR results by DFT calculations. J.Mol. Struct. 2009;936,46-55.
- Unver Y, Deniz S, Celik F, Akar Z, Kucuk M, Sancak K. Synthesis Of New 1,2,4-Triazole Compounds Containing Schiff And Mannich Bases (Morpholine) with Antioxidant And Antimicrobial Activities. Journal Of Enzym Inhibition and Medicinal Chemistry. 2016;31(3):89-95.
- Unver Y, Deniz S, Celik F, Akar Z, Kucuk M, Sancak K. Synthesis Of New 1,2,4-Triazole Compounds Containing Schiff And Mannich Bases (Morpholine) with Antioxidant And Antimicrobial Activities. Journal Of Enzym Inhibition and Medicinal Chemistry. 2016;31(3):89-95.
- Unver Y, Sancak K, Celik F, Birinci E, Kucuk M, Soylu S, et al. New Thiophene-1,2,4-Triazole-5(3)-Ones: Highly Bioactive Thiosemicarbazides, Structures Of Schiff Bases And Triazole-Thiols, European Journal Of Medicinal Chemistry. 2014;84 639-650.
- Unver Y, Sancak K, Celik F, Birinci E, Kucuk M, Soylu S, et al. New Thiophene-1,2,4-Triazole-5(3)-Ones: Highly Bioactive Thiosemicarbazides, Structures Of Schiff Bases And Triazole-Thiols, European Journal Of Medicinal Chemistry. 2014;84 639-650.
- Suleymanoglu N, Ustabas R, Direkel S, Bingöl Alpaslan Y, Unver Y. 1,2,4- Triazole Derivatives With Morpholine; Dft Study And Antileishmanial Activity. Canadian Journal Of Physics, 2018;96(7):719-723.
- Suleymanoglu N, Ustabas R, Direkel S, Bingöl Alpaslan Y, Unver Y. 1,2,4- Triazole Derivatives With Morpholine; Dft Study And Antileishmanial Activity. Canadian Journal Of Physics, 2018;96(7):719-723.
- Ikizler AA, Ucar F, Yuskek H, Aytin A, Yasa I, Gezer T. Synthesis and antifungal activity of some new arylidenamino compounds. Acta Pol Pharm, 1997; 54(2), 135-140).
- Ikizler AA, Ucar F, Yuskek H, Aytin A, Yasa I, Gezer T. Synthesis and antifungal activity of some new arylidenamino compounds. Acta Pol Pharm, 1997; 54(2), 135-140).
- Sumrra SH, Zafar W, Imran M, Chohan ZH. A review on the biomedical efficacy of transition metal triazole compounds. Journal of Coordination Chemistry. 2022;75(3-4): 293–334. DOI: 10.1080/00958972.2022.2059359
- Sumrra SH, Zafar W, Imran M, Chohan ZH. A review on the biomedical efficacy of transition metal triazole compounds. Journal of Coordination Chemistry. 2022;75(3-4): 293–334. DOI: 10.1080/00958972.2022.2059359
- Sancak B. Staphylococcus aureus And Antibiotic Resistance. Mikrobiyol Bul, 2011; 45(3):565-576.
- Sancak B. Staphylococcus aureus And Antibiotic Resistance. Mikrobiyol Bul, 2011; 45(3):565-576.
- Gazi H, Kurutepe S, Surucuoglu S, Ecemis T, Özbakkaloglu B. Antimicrobial Resistance in Hospital-Acquired Enterococcus Faecalis and Enterococcus Faecium Strains. Ankem Dergisi, 2004;18(1):49-52.
- Gazi H, Kurutepe S, Surucuoglu S, Ecemis T, Özbakkaloglu B. Antimicrobial Resistance in Hospital-Acquired Enterococcus Faecalis and Enterococcus Faecium Strains. Ankem Dergisi, 2004;18(1):49-52.
- Savasan S, Kaya O, Kirkan S, Ciftci A. Antibiotic resistance of fish-derived Enterococcus faecalis strains. Journal of Ankara University Faculty of Veterinary Medicine, 2008;55(2):107-110.
- Savasan S, Kaya O, Kirkan S, Ciftci A. Antibiotic resistance of fish-derived Enterococcus faecalis strains. Journal of Ankara University Faculty of Veterinary Medicine, 2008;55(2):107-110.
- Ciftci İH, Asık G. Antibiotic Resistance Mechanisms of Acinetobacter baumannii. Ankem Derg. 2011;25(3), 196-207.
- Ciftci İH, Asık G. Antibiotic Resistance Mechanisms of Acinetobacter baumannii. Ankem Derg. 2011;25(3), 196-207.
- Benkli K. Synthesis of Some 3-Arylamino-5-Aryloxymethyl [1, 2, 4] Triazole Derivatives and Investigation of their Antimicrobial Effects. Eskisehir: Anadolu University Health Sciences Institute. 2000.
- Benkli K. Synthesis of Some 3-Arylamino-5-Aryloxymethyl [1, 2, 4] Triazole Derivatives and Investigation of their Antimicrobial Effects. Eskisehir: Anadolu University Health Sciences Institute. 2000.
- Ozkanlı F, Dalkara S, Yulug N. Antibacterial and Antifungal Effect Studies on Some 2-Acetonaphtone and P-Chloroacetophenone Derivatives. Fabad J. Pharm. Sci, 1991;16:17-22.
- Ozkanlı F, Dalkara S, Yulug N. Antibacterial and Antifungal Effect Studies on Some 2-Acetonaphtone and P-Chloroacetophenone Derivatives. Fabad J. Pharm. Sci, 1991;16:17-22.
- Kocak G, Akdemir E. Anticancer, Apoptotic and Antibacterial Effects of Thiosemicarbazide and Bis-1, 2, 4-Triazole Derivatives. Bitlis Eren University Journal of Science. 2020;9(3):1124-1133.
- Kocak G, Akdemir E. Anticancer, Apoptotic and Antibacterial Effects of Thiosemicarbazide and Bis-1, 2, 4-Triazole Derivatives. Bitlis Eren University Journal of Science. 2020;9(3):1124-1133.
- Login CC, Bâldea I, Tiperciuc B, Benedec D, Vodnar DC, Decea N, et al. Thiazolyl Schiff Base: Antibacterial and Antifungal Effects and In Vitro Oxidative Stress Modulation on Human Endothelial Cells. Oxid Med Cell Longev. 2019; Volume 2019, Article ID 1607903, doi: 10.1155/2019/1607903.
- Login CC, Bâldea I, Tiperciuc B, Benedec D, Vodnar DC, Decea N, et al. Thiazolyl Schiff Base: Antibacterial and Antifungal Effects and In Vitro Oxidative Stress Modulation on Human Endothelial Cells. Oxid Med Cell Longev. 2019; Volume 2019, Article ID 1607903, doi: 10.1155/2019/1607903.
- Chohan ZH, Hanif M. Antibacterial and antifungal metal based triazole Schiff bases. J Enzyme Inhib Med Chem. 2023;(5):944-53. doi: 10.3109/14756366.2012.696246.
- Chohan ZH, Hanif M. Antibacterial and antifungal metal based triazole Schiff bases. J Enzyme Inhib Med Chem. 2023;(5):944-53. doi: 10.3109/14756366.2012.696246.
- Strzelecka M, Świątek P. 1,2,4-Triazoles as Important Antibacterial Agents. Pharmaceuticals (Basel). 2021;14(3):224. doi: 10.3390/ph14030224.
- Strzelecka M, Świątek P. 1,2,4-Triazoles as Important Antibacterial Agents. Pharmaceuticals (Basel). 2021;14(3):224. doi: 10.3390/ph14030224.
- Holanda VN, Silva WVD, Nascimento PHD, Silva SRB, Cabral Filho PE, Assis SPO, et al. Antileishmanial activity of 4-phenyl-1-[2-(phthalimido-2-yl)ethyl]-1H-1,2,3-triazole (PT4) derivative on Leishmania amazonensis and Leishmania braziliensis: In silico ADMET, in vitro activity, docking and molecular dynamic simulations. Bioorg Chem. 2020; 105:104437. doi: 10.1016/j.bioorg.104437.
- Holanda VN, Silva WVD, Nascimento PHD, Silva SRB, Cabral Filho PE, Assis SPO, et al. Antileishmanial activity of 4-phenyl-1-[2-(phthalimido-2-yl)ethyl]-1H-1,2,3-triazole (PT4) derivative on Leishmania amazonensis and Leishmania braziliensis: In silico ADMET, in vitro activity, docking and molecular dynamic simulations. Bioorg Chem. 2020; 105:104437. doi: 10.1016/j.bioorg.104437.
- Meinel RS, Almeida ADC, Stroppa PHF, Glanzmann N, Coimbra ES, da Silva AD. Novel functionalized 1,2,3-triazole derivatives exhibit antileishmanial activity, increase in total and mitochondrial-ROS and depolarization of mitochondrial membrane potential of Leishmania amazonensis. Chem Biol Interact. 2020;315:108850. doi: 10.1016/j.cbi.
- Meinel RS, Almeida ADC, Stroppa PHF, Glanzmann N, Coimbra ES, da Silva AD. Novel functionalized 1,2,3-triazole derivatives exhibit antileishmanial activity, increase in total and mitochondrial-ROS and depolarization of mitochondrial membrane potential of Leishmania amazonensis. Chem Biol Interact. 2020;315:108850. doi: 10.1016/j.cbi.
- das Chagas Almeida A, Meinel RS, Leal YL, Silva T P, Glanzmann N, Mendonca D V C, et al. Functionalized 1,2,3-triazolium salts as potential agents against visceral leishmaniasis. Parasitol Res. 2022;121(5):1389-1406. doi:10.1007/s00436-022-07431-9.
- das Chagas Almeida A, Meinel RS, Leal YL, Silva T P, Glanzmann N, Mendonca D V C, et al. Functionalized 1,2,3-triazolium salts as potential agents against visceral leishmaniasis. Parasitol Res. 2022;121(5):1389-1406. doi:10.1007/s00436-022-07431-9.
- Suleymanoglu N, Unver Y, Ustabas R, Direkel S, Alpaslan G. Antileishmanial activity study and theoretical calculations for 4-amino-1, 2, 4-triazole derivatives. Journal of Molecular Structure. 2017;1144:80-86
- Suleymanoglu N, Unver Y, Ustabas R, Direkel S, Alpaslan G. Antileishmanial activity study and theoretical calculations for 4-amino-1, 2, 4-triazole derivatives. Journal of Molecular Structure. 2017;1144:80-86
- Chen Y, Li P, Su S, Chen M, He J, Liu L, et al. Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base. RSC Adv. 2019;9(40):23045-23052. doi: 10.1039/c9ra05139b.
- Chen Y, Li P, Su S, Chen M, He J, Liu L, et al. Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base. RSC Adv. 2019;9(40):23045-23052. doi: 10.1039/c9ra05139b.