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Synthesis of Some New Benzoxazole Derivatives and Antimicrobial and Cytotoxic Activity Studies

Yıl 2021, Sayı: 21, 455 - 462, 31.01.2021
https://doi.org/10.31590/ejosat.822417

Öz

There is an urgent need to develop new antimicrobial drugs due to the rapid development of resistance to increasing microbial infectious diseases and drugs used in their treatment. Also, the compounds synthesized for use in cancer treatment limit their use due to their cytotoxic effect on normal cells and cancerous cells, and their side effects are high. For this reason, researches continue to intensify the drugs developed for cancer treatment to be selectively effective on cancer cells and to reduce their side effects as much as possible. Within this study's scope, 7 compounds of 2-(p-substituted phenyl)-5-(2-substitutedacetamido) were synthesized in 3 steps, 2 of which were original, and their structures were illuminated by HRMS, 1H-NMR, and 13C-NMR spectroscopy methods. Antimicrobial effects on 10 different microorganisms were evaluated. In addition, cytotoxic activities were investigated on MCF-7 and A549 cell lines by the MTT method. As a result of the study, it was determined that the synthesized compounds were both antibacterial and antifungal at MIC values ranging from 64-256 µg/mL, and compound 7 had significant cytotoxic activity on both A549 and MCF-7. The results obtained will make an important contribution to the studies conducted to develop new or alternative antimicrobial and cytotoxic agents.

Destekleyen Kurum

Erciyes University Scientific Research Projects Coordination Unit

Proje Numarası

THD-2020-10038

Teşekkür

This work has been supported by Erciyes University Scientific Research Projects Coordination Unit with research project THD-2020-10038. NMR analysis of the compounds were performed by Erciyes University Technology and Research Center (TAUM) and HRMS analysis were performed by Bilkent University National Nanotechnology Research Center (UNAM).

Kaynakça

  • Alanis, A. J. (2005). Resistance to antibiotics: are we in the post-antibiotic era? Archives of medical research, 36(6), 697-705.
  • Alper-Hayta, S., Arisoy, M., Temiz-Arpaci, Ö., Yildiz, I., Aki, E., Özkan, S., & Kaynak, F. (2008). Synthesis, antimicrobial activity, pharmacophore analysis of some new 2-(substitutedphenyl/benzyl)-5-[(2-benzofuryl) carboxamido] benzoxazoles. European Journal of Medicinal Chemistry, 43(11), 2568-2578.
  • Arandjelovic, P., Doerflinger, M., & Pellegrini, M. (2019). Current and emerging therapies to combat persistent intracellular pathogens. Current opinion in pharmacology, 48, 33-39.
  • Arisoy, M., Temiz-Arpaci, O., Yildiz, I., Kaynak-Onurdag, F., Aki, E., Yalcin, I., & Abbasoglu, U. (2008). Synthesis, antimicrobial activity and QSAR studies of 2, 5-disubstituted benzoxazoles. SAR and QSAR in Environmental Research, 19(5-6), 589-612.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2012). Synthesis and antimicrobial activity of novel benzoxazoles. Zeitschrift für Naturforschung C, 67(9-10), 466-472.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2013). Novel benzoxazoles: synthesis and antibacterial, antifungal, and antitubercular activity against antibiotic-resistant and-sensitive microbes. Zeitschrift für Naturforschung C, 68(11-12), 453-460.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2014). Synthesis and Antimicrobial Evaluation of 2-(p-Substituted Phenyl)-5-[(4-substituted piperazin-1-yl) acetamido]-benzoxazoles. Zeitschrift für Naturforschung C, 69(9-10), 368-374.
  • CaLSI, C. (2018). Performance Standards for Antimicrobial Susceptibility Testing: Approved Twenty-: Document M100-S28. Wayne, PA, USA: CLSI, 2018.
  • Celik, I., Erol, M., Temiz Arpaci, O., Sezer Senol, F., & Erdogan Orhan, I. (2020). Evaluation of activity of some 2, 5-disubstituted benzoxazole derivatives against acetylcholinesterase, butyrylcholinesterase and tyrosinase: ADME prediction, DFT and comparative molecular docking studies. Polycyclic Aromatic Compounds, 1-12.
  • Cheminformatics, M. (2018). Calculation of molecular properties and bioactivity score. Computer software]. Retrieved from http://www. molinspiration. com/cgi-bin/properties.
  • Edition, A. S.-S. (2007). CLSI document H3-A6. Wayne (PA): CLSI.
  • Erol, M., Celik, I., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Okten, S. (2020). Design, synthesis, molecular docking, density functional theory and antimicrobial studies of some novel benzoxazole derivatives as structural bioisosteres of nucleotides. Journal of Biomolecular Structure and Dynamics, 1-12.
  • Fernández, Y., Cueva, J., Palomo, A. G., Ramos, M., de Juan, A., Calvo, L., García-Mata, J., García-Teijido, P., Peláez, I., & García-Estévez, L. (2010). Novel therapeutic approaches to the treatment of metastatic breast cancer. Cancer treatment reviews, 36(1), 33-42.
  • Han, S.-Y., Lee, C. O., Ahn, S.-H., Lee, M.-O., Kang, S.-Y., Cha, H.-J., Cho, S. Y., Du Ha, J., Ryu, J. W., & Jung, H. (2012). Evaluation of a multi-kinase inhibitor KRC-108 as an anti-tumor agent in vitro and in vivo. Investigational new drugs, 30(2), 518-523.
  • Jonckers, T. H., Rouan, M.-C., Haché, G., Schepens, W., Hallenberger, S., Baumeister, J., & Sasaki, J. C. (2012). Benzoxazole and benzothiazole amides as novel pharmacokinetic enhancers of HIV protease inhibitors. Bioorganic & medicinal chemistry letters, 22(15), 4998-5002.
  • Kilic-Kurt, Z., Bakar-Ates, F., & Bahat, M. (2019). N, N′-diaryl urea derivatives: Molecular docking, molecular properties prediction and anticancer evaluation. Journal of Molecular Structure, 1193, 239-246. Lipinski, C. A. (2004). Lead-and drug-like compounds: the rule-of-five revolution. Drug Discovery Today: Technologies, 1(4), 337-341.
  • Molsoft, L. (2004). ICM software manual. In: Version. https://www.molsoft.com/.
  • Oehlers, L., Mazzitelli, C. L., Brodbelt, J. S., Rodriguez, M., & Kerwin, S. (2004). Evaluation of complexes of DNA duplexes and novel benzoxazoles or benzimidazoles by electrospray ionization mass spectrometry. Journal of the American Society for Mass Spectrometry, 15(11), 1593-1603.
  • Oksuzoglu, E., Tekiner-Gulbas, B., Alper, S., Temiz-Arpaci, O., Ertan, T., Yildiz, I., Diril, N., Sener-Aki, E., & Yalcin, I. (2008). Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors. Journal of enzyme inhibition and medicinal chemistry, 23(1), 37-42.
  • Sakamoto, T., Cullen, M. D., Hartman, T. L., Watson, K. M., Buckheit, R. W., Pannecouque, C., De Clercq, E., & Cushman, M. (2007). Synthesis and anti-HIV activity of new metabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1, 2, 4-oxadiazole systems. Journal of medicinal chemistry, 50(14), 3314-3321.
  • Sondhi, S. M., Singh, N., Kumar, A., Lozach, O., & Meijer, L. (2006). Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases. Bioorganic & medicinal chemistry, 14(11), 3758-3765.
  • Suzuki, H., Asakawa, A., Amitani, H., Nakamura, N., & Inui, A. (2013). Cancer cachexia—pathophysiology and management. Journal of gastroenterology, 48(5), 574-594.
  • Taşcı, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Okten, S. (2018). Synthesis and antimicrobial evaluation of novel 5-substituted-2-(p-tert-butylphenyl) benzoxazoles.
  • Temiz-Arpaci, O., Arisoy, M., Sac, D., Doganc, F., Tasci, M., Senol, F. S., & Orhan, I. E. (2016). Biological evaluation and docking studies of some benzoxazole derivatives as inhibitors of acetylcholinesterase and butyrylcholinesterase. Zeitschrift für Naturforschung C, 71(11-12), 409-413.
  • Wei, C.-X., Guan, L.-P., Jia, J.-H., Chai, K.-Y., & Quan, Z.-S. (2009). Synthesis of 2-substituted-6-(4H-1,2,4-triazol-4-yl) benzo [d] oxazoles as potential anticonvulsant agents. Archives of pharmacal research, 32(1), 23-31.
  • Yeliz, U., Özkan, A. İ., & Tolan, V. Synthesis of New p-Alkylaminophenol Compounds and Investigation of Their Antimicrobial and Antioxidant Activity. Avrupa Bilim ve Teknoloji Dergisi(16), 701-706.
  • Yilmaz, S., Yalcin, I., Okten, S., Onurdag, F., & Aki-Yalcin, E. (2017). Synthesis and investigation of binding interactions of 1, 4-benzoxazine derivatives on topoisomerase IV in Acinetobacter baumannii. SAR and QSAR in Environmental Research, 28(11), 941-956.
  • Zilifdar, F., Foto, E., Ertan‐Bolelli, T., Aki‐Yalcin, E., Yalcin, I., & Diril, N. (2018). Biological evaluation and pharmacophore modeling of some benzoxazoles and their possible metabolites. Archiv der Pharmazie, 351(2), 1700265.

Bazı Yeni Benzoksazol Türevlerinin Sentezi ve Antimikrobiyal ve Sitotoksik Aktivite Çalışmaları

Yıl 2021, Sayı: 21, 455 - 462, 31.01.2021
https://doi.org/10.31590/ejosat.822417

Öz

Artan mikrobiyal enfeksiyon hastalıklara ve bunların tedavisinde kullanılan ilaçlara karşı hızla direnç gelişmesi nedeniyle yeni antimikrobiyal ilaçların geliştirilmesine acil ihtiyaç duyulmaktadır. Ayrıca kanser tedavisinde kullanmak amacıyla sentezlenen bileşiklerin kanserli hücrelerde olduğu kadar normal hücrelerde de sitotoksik etki göstermesi ve yan etkilerinin fazla olması nedeniyle kullanımını sınırlı hale getirmektedir. Bu nedenle kanser tedavisi için geliştirilen ilaçların seçici olarak kanserli hücreler üzerinde etkili olması ve yan etkilerinin mümkün olduğunca azaltılması yönünde araştırmalar yoğun olarak devam etmektedir. Bu çalışma kapsamında 2'si orjinal olmayan 7 tane 2-(p-substitutedphenyl)-5-(2-substitutedacetamido) bileşiğinin 3 basamakta sentezi gerçekleştirildi, yapıları HRMS, 1H-NMR ve 13C-NMR spektrokpisi yöntemleri ile aydınlatıldı. 10 farklı mikroorganizma üzerinde antimikrobiyal etkileri değerlendirildi. Ayrıca MCF-7 ve A549 hüzre hatları üzerinde MTT metodu ile sitotoksik aktiviteleri araştırıldı. Çalışma sonucunda sentezlenen bileşiklerin 64-256 µg/mL arasında değişen MİK değerlerinde hem antibakteriyel hem de antifungal etkili oldukarı belirlenmiş ve bileşik 7'nin hem A549 hem de MCF-7 üzerinde önemli sitotoksik aktivitesi bulunmuştur. Elde edilen sonuçlar yeni veya alternatif ilaç antimikrobiyal ve sitotoksik ajan geliştirmek için yapılan çalışmalara önemli bir katkı sağlayacaktır.

Proje Numarası

THD-2020-10038

Kaynakça

  • Alanis, A. J. (2005). Resistance to antibiotics: are we in the post-antibiotic era? Archives of medical research, 36(6), 697-705.
  • Alper-Hayta, S., Arisoy, M., Temiz-Arpaci, Ö., Yildiz, I., Aki, E., Özkan, S., & Kaynak, F. (2008). Synthesis, antimicrobial activity, pharmacophore analysis of some new 2-(substitutedphenyl/benzyl)-5-[(2-benzofuryl) carboxamido] benzoxazoles. European Journal of Medicinal Chemistry, 43(11), 2568-2578.
  • Arandjelovic, P., Doerflinger, M., & Pellegrini, M. (2019). Current and emerging therapies to combat persistent intracellular pathogens. Current opinion in pharmacology, 48, 33-39.
  • Arisoy, M., Temiz-Arpaci, O., Yildiz, I., Kaynak-Onurdag, F., Aki, E., Yalcin, I., & Abbasoglu, U. (2008). Synthesis, antimicrobial activity and QSAR studies of 2, 5-disubstituted benzoxazoles. SAR and QSAR in Environmental Research, 19(5-6), 589-612.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2012). Synthesis and antimicrobial activity of novel benzoxazoles. Zeitschrift für Naturforschung C, 67(9-10), 466-472.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2013). Novel benzoxazoles: synthesis and antibacterial, antifungal, and antitubercular activity against antibiotic-resistant and-sensitive microbes. Zeitschrift für Naturforschung C, 68(11-12), 453-460.
  • Arisoy, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Ozgen, S. (2014). Synthesis and Antimicrobial Evaluation of 2-(p-Substituted Phenyl)-5-[(4-substituted piperazin-1-yl) acetamido]-benzoxazoles. Zeitschrift für Naturforschung C, 69(9-10), 368-374.
  • CaLSI, C. (2018). Performance Standards for Antimicrobial Susceptibility Testing: Approved Twenty-: Document M100-S28. Wayne, PA, USA: CLSI, 2018.
  • Celik, I., Erol, M., Temiz Arpaci, O., Sezer Senol, F., & Erdogan Orhan, I. (2020). Evaluation of activity of some 2, 5-disubstituted benzoxazole derivatives against acetylcholinesterase, butyrylcholinesterase and tyrosinase: ADME prediction, DFT and comparative molecular docking studies. Polycyclic Aromatic Compounds, 1-12.
  • Cheminformatics, M. (2018). Calculation of molecular properties and bioactivity score. Computer software]. Retrieved from http://www. molinspiration. com/cgi-bin/properties.
  • Edition, A. S.-S. (2007). CLSI document H3-A6. Wayne (PA): CLSI.
  • Erol, M., Celik, I., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Okten, S. (2020). Design, synthesis, molecular docking, density functional theory and antimicrobial studies of some novel benzoxazole derivatives as structural bioisosteres of nucleotides. Journal of Biomolecular Structure and Dynamics, 1-12.
  • Fernández, Y., Cueva, J., Palomo, A. G., Ramos, M., de Juan, A., Calvo, L., García-Mata, J., García-Teijido, P., Peláez, I., & García-Estévez, L. (2010). Novel therapeutic approaches to the treatment of metastatic breast cancer. Cancer treatment reviews, 36(1), 33-42.
  • Han, S.-Y., Lee, C. O., Ahn, S.-H., Lee, M.-O., Kang, S.-Y., Cha, H.-J., Cho, S. Y., Du Ha, J., Ryu, J. W., & Jung, H. (2012). Evaluation of a multi-kinase inhibitor KRC-108 as an anti-tumor agent in vitro and in vivo. Investigational new drugs, 30(2), 518-523.
  • Jonckers, T. H., Rouan, M.-C., Haché, G., Schepens, W., Hallenberger, S., Baumeister, J., & Sasaki, J. C. (2012). Benzoxazole and benzothiazole amides as novel pharmacokinetic enhancers of HIV protease inhibitors. Bioorganic & medicinal chemistry letters, 22(15), 4998-5002.
  • Kilic-Kurt, Z., Bakar-Ates, F., & Bahat, M. (2019). N, N′-diaryl urea derivatives: Molecular docking, molecular properties prediction and anticancer evaluation. Journal of Molecular Structure, 1193, 239-246. Lipinski, C. A. (2004). Lead-and drug-like compounds: the rule-of-five revolution. Drug Discovery Today: Technologies, 1(4), 337-341.
  • Molsoft, L. (2004). ICM software manual. In: Version. https://www.molsoft.com/.
  • Oehlers, L., Mazzitelli, C. L., Brodbelt, J. S., Rodriguez, M., & Kerwin, S. (2004). Evaluation of complexes of DNA duplexes and novel benzoxazoles or benzimidazoles by electrospray ionization mass spectrometry. Journal of the American Society for Mass Spectrometry, 15(11), 1593-1603.
  • Oksuzoglu, E., Tekiner-Gulbas, B., Alper, S., Temiz-Arpaci, O., Ertan, T., Yildiz, I., Diril, N., Sener-Aki, E., & Yalcin, I. (2008). Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors. Journal of enzyme inhibition and medicinal chemistry, 23(1), 37-42.
  • Sakamoto, T., Cullen, M. D., Hartman, T. L., Watson, K. M., Buckheit, R. W., Pannecouque, C., De Clercq, E., & Cushman, M. (2007). Synthesis and anti-HIV activity of new metabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1, 2, 4-oxadiazole systems. Journal of medicinal chemistry, 50(14), 3314-3321.
  • Sondhi, S. M., Singh, N., Kumar, A., Lozach, O., & Meijer, L. (2006). Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases. Bioorganic & medicinal chemistry, 14(11), 3758-3765.
  • Suzuki, H., Asakawa, A., Amitani, H., Nakamura, N., & Inui, A. (2013). Cancer cachexia—pathophysiology and management. Journal of gastroenterology, 48(5), 574-594.
  • Taşcı, M., Temiz-Arpaci, O., Kaynak-Onurdag, F., & Okten, S. (2018). Synthesis and antimicrobial evaluation of novel 5-substituted-2-(p-tert-butylphenyl) benzoxazoles.
  • Temiz-Arpaci, O., Arisoy, M., Sac, D., Doganc, F., Tasci, M., Senol, F. S., & Orhan, I. E. (2016). Biological evaluation and docking studies of some benzoxazole derivatives as inhibitors of acetylcholinesterase and butyrylcholinesterase. Zeitschrift für Naturforschung C, 71(11-12), 409-413.
  • Wei, C.-X., Guan, L.-P., Jia, J.-H., Chai, K.-Y., & Quan, Z.-S. (2009). Synthesis of 2-substituted-6-(4H-1,2,4-triazol-4-yl) benzo [d] oxazoles as potential anticonvulsant agents. Archives of pharmacal research, 32(1), 23-31.
  • Yeliz, U., Özkan, A. İ., & Tolan, V. Synthesis of New p-Alkylaminophenol Compounds and Investigation of Their Antimicrobial and Antioxidant Activity. Avrupa Bilim ve Teknoloji Dergisi(16), 701-706.
  • Yilmaz, S., Yalcin, I., Okten, S., Onurdag, F., & Aki-Yalcin, E. (2017). Synthesis and investigation of binding interactions of 1, 4-benzoxazine derivatives on topoisomerase IV in Acinetobacter baumannii. SAR and QSAR in Environmental Research, 28(11), 941-956.
  • Zilifdar, F., Foto, E., Ertan‐Bolelli, T., Aki‐Yalcin, E., Yalcin, I., & Diril, N. (2018). Biological evaluation and pharmacophore modeling of some benzoxazoles and their possible metabolites. Archiv der Pharmazie, 351(2), 1700265.
Toplam 28 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Meryem Erol 0000-0001-5676-098X

İsmail Çelik 0000-0002-8146-1663

Gülcan Kuyucuklu 0000-0003-1596-1659

Ebru Uzunhisarcıklı 0000-0002-7088-7490

Proje Numarası THD-2020-10038
Yayımlanma Tarihi 31 Ocak 2021
Yayımlandığı Sayı Yıl 2021 Sayı: 21

Kaynak Göster

APA Erol, M., Çelik, İ., Kuyucuklu, G., Uzunhisarcıklı, E. (2021). Synthesis of Some New Benzoxazole Derivatives and Antimicrobial and Cytotoxic Activity Studies. Avrupa Bilim Ve Teknoloji Dergisi(21), 455-462. https://doi.org/10.31590/ejosat.822417