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BENZOİL TİYOÜRE TÜREVLERİNİN SENTEZİ, ANTİFUNGAL AKTİVİTESİNİN VE İLAÇ OLABİLİRLİĞİNİN DEĞERLENDİRİLMESİ

Year 2025, Volume: 24 Issue: 47, 217 - 228, 30.06.2025
https://doi.org/10.55071/ticaretfbd.1588118

Abstract

Bu çalışmada, bir dizi 2-bromobenzoil tiyoüre türevleri sentezlenmiştir. Sentezlenen tiyoürelerin yapıları spektroskopik yöntemlerle tanımlanmıştır. Bu türevler, daha önce sentezlenen 2-florobenzoil tiyoürelerle birlikte, potansiyel antifungal aktiviteleri açısından değerlendirilmiştir. Bileşik 2d ve 2f, Candida albicans'a karşı antifungal aktivite göstermiştir. Bileşik 2f ayrıca C. parapsilosis'e karşı aktivite göstermiştir. Bileşiklerin ilaç olabilirlik özellikleri de tahmin edilmiş ve tüm bileşiklerin iyi ilaç olabilirlik özellikleri gösterdiği bulunmuştur.

References

  • Agili, F.A. (2024). Biological Applications of Thiourea Derivatives: Detailed Review. Chemistry. 6(3), 435-468. https://doi.org/10.3390/chemistry6030025
  • Anna, B., Agnieszka, G., Ewa, A., Jolanta, O., Dagmara, K., Marta, S. (2023). In vitro antimycobacterial activity and interaction profiles of diaryl thiourea-copper (II) complexes with antitubercular drugs against Mycobacterium tuberculosis isolates. Tuberculosis. 143, 102412. https://doi.org/10.1016/j.tube.2023.102412
  • Calixto S.D., Simão T.L.B.V., Palmeira-Mello M.V., Viana G.M., Assumpção P.W.M.C., Rezende M.G., Santo C.C.E., Mussi V.O., Rodrigues C.R., Lasunskaia E., Souza A. M. T., Cabral L.M., Muzitano M.F. (2022). Antimycobacterial and anti-inflammatory activities of thiourea derivatives focusing on treatment approaches for severe pulmonary tuberculosis. Bioorg. Med. Chem. 53, 116506. https://doi.org/10.1016/j.bmc.2021.116506
  • Canudo-Barreras, G., Ortego, L., Izaga, A., Marzo, I., Herrera, R. P., & Gimeno, M. C. (2021). Synthesis of New Thiourea-Metal Complexes with Promising Anticancer Properties. Molecules, 26(22), 6891. https://doi.org/10.3390/molecules26226891
  • Clinical and Laboratory Standards Institute (CLSI). 2008. Reference method for broth dilution antifungal susceptibility testing of yeasts; approved standard, 3rd ed; CLSI document M27-A3. Clinical and Laboratory Standards Institute, Wayne, PA.
  • Daina A, Michielin O, Zoete V. (2017). SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci Rep. 7, 42717. https://doi.org/10.1038/srep42717
  • Daina A., Zoete V. (2016). A BOILED-Egg to predict gastrointestinal absorption and brain penetration of small molecules, ChemMedChem, 11, 1117–1121. https://doi.org/10.1002/cmdc.201600182
  • Dey S., Patel A., Haloi N., Srimayee S., Paul S., Barik G.K., Akhtar N., Shaw D., Hazarika G., Prusty B.M., Kumar, Santra M.K., Tajkhorshid E., Bhattacharjee S., Manna D. (2023). Quinoline Thiourea-Based Zinc Ionophores with Antibacterial Activity. J. Med. Chem. 66 (16), 11078-11093 https://doi.org/10.1021/acs.jmedchem.3c00368
  • Erol Günal, Ş. (2023). Synthesis Of 2-Fluorobenzoyl Thiourea Derivatives. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi, 22(44), 417-424. https://doi.org/10.55071/ticaretfbd.1364818
  • Hroch L., Guest P., Benek O., Soukup O., Janockova J., Dolezal R., Kuca K., Aitken L., Smith T.K., Gunn-Moore F., Zala D., Ramsay R.R., Musilek K. (2017). Synthesis and evaluation of frentizole-based indolyl thiourea analogues as MAO/ABAD inhibitors for Alzheimer’s disease treatment. Bioorg. Med. Chem. 25(3), 1143-1152. https://doi.org/10.1016/j.bmc.2016.12.029
  • Potts R.O., Guy R.H. (1992). Predicting skin permeability, Pharm. Res. 9, 663–669 https://doi.org/10.1023/a:1015810312465
  • Riccardo, R., Giada, M., Andrea, C., Antimo, G., Emidio, C. (2021). Recent advances in urea- and thiourea-containing compounds: Focus on innovative approaches in medicinal chemistry and organic synthesis. RSC Med. Chem. 12(7), 1046–1064. https://doi.org/10.1039/D1MD00058F
  • Seo, H., Kohlbrand, A.J., Stokes, R.W., Chung, J., Cohen, S.M. (2023). Masking thiol reactivity with thioamide, thiourea, and thiocarbamate-based MBPs. Chem. Commun. 59(16), 2283– 2286. https://doi.org/10.1039/D2CC06596G
  • Shivakumara, K.N., Sridhar, B.T. (2021). Review on role of urea and thiourea derivatives of some heterocyclic Scaffold in drug design and medicinal chemistry. Int. J. Chem. Res. Dev. 3(1), 20–25. https://doi.org/10.33545/26646552.2021.v3.i1a.23
  • Shulgau Z., Palamarchuk I., Sergazy S., Urazbayeva A., Gulyayev A., Ramankulov Y., Kulakov. I. (2024). Synthesis, Computational Study, and In Vitro α-Glucosidase Inhibitory Action of Thiourea Derivatives Based on 3-Aminopyridin-2(1H)-Ones. Molecules. 29(15), 3627. https://doi.org/10.3390/molecules29153627
  • Strzyga-Łach, P., Chrzanowska, A., Podsadni, K., Bielenica, A. (2021). Investigation of the Mechanisms of Cytotoxic Activity of 1,3-Disubstituted Thiourea Derivatives. Pharmaceuticals, 14, 1097. https://doi.org/10.3390/ph14111097
  • Yaqeen, M.A. Rafid, H.A. (2023). Synthesis, Anti-breast Cancer Activity, and Molecular Docking Studies of Thiourea Benzamide Derivatives and Their Complexes with Copper Ion. Trop. J. Nat. Prod. Res. 7(6), 3158–3167. http://www.doi.org/10.26538/tjnpr/v7i6.15

SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES

Year 2025, Volume: 24 Issue: 47, 217 - 228, 30.06.2025
https://doi.org/10.55071/ticaretfbd.1588118

Abstract

Herein, we report the synthesis of a series of 2-bromobenzoyl-substituted thiourea derivatives. The structures of the synthesized thioureas were characterized by spectroscopic methods. These derivatives, together with 2-fluorobenzoyl thioureas synthesized previously, have been evaluated for their potential antifungal activity. Compounds 2d and 2f showed antifungal activity against Candida albicans. Compound 2f also demonstrated activity against C. parapsilosis. Drug-likeness properties of the compounds were also estimated, and it was found that all compounds showed good drug-likeness properties.

References

  • Agili, F.A. (2024). Biological Applications of Thiourea Derivatives: Detailed Review. Chemistry. 6(3), 435-468. https://doi.org/10.3390/chemistry6030025
  • Anna, B., Agnieszka, G., Ewa, A., Jolanta, O., Dagmara, K., Marta, S. (2023). In vitro antimycobacterial activity and interaction profiles of diaryl thiourea-copper (II) complexes with antitubercular drugs against Mycobacterium tuberculosis isolates. Tuberculosis. 143, 102412. https://doi.org/10.1016/j.tube.2023.102412
  • Calixto S.D., Simão T.L.B.V., Palmeira-Mello M.V., Viana G.M., Assumpção P.W.M.C., Rezende M.G., Santo C.C.E., Mussi V.O., Rodrigues C.R., Lasunskaia E., Souza A. M. T., Cabral L.M., Muzitano M.F. (2022). Antimycobacterial and anti-inflammatory activities of thiourea derivatives focusing on treatment approaches for severe pulmonary tuberculosis. Bioorg. Med. Chem. 53, 116506. https://doi.org/10.1016/j.bmc.2021.116506
  • Canudo-Barreras, G., Ortego, L., Izaga, A., Marzo, I., Herrera, R. P., & Gimeno, M. C. (2021). Synthesis of New Thiourea-Metal Complexes with Promising Anticancer Properties. Molecules, 26(22), 6891. https://doi.org/10.3390/molecules26226891
  • Clinical and Laboratory Standards Institute (CLSI). 2008. Reference method for broth dilution antifungal susceptibility testing of yeasts; approved standard, 3rd ed; CLSI document M27-A3. Clinical and Laboratory Standards Institute, Wayne, PA.
  • Daina A, Michielin O, Zoete V. (2017). SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci Rep. 7, 42717. https://doi.org/10.1038/srep42717
  • Daina A., Zoete V. (2016). A BOILED-Egg to predict gastrointestinal absorption and brain penetration of small molecules, ChemMedChem, 11, 1117–1121. https://doi.org/10.1002/cmdc.201600182
  • Dey S., Patel A., Haloi N., Srimayee S., Paul S., Barik G.K., Akhtar N., Shaw D., Hazarika G., Prusty B.M., Kumar, Santra M.K., Tajkhorshid E., Bhattacharjee S., Manna D. (2023). Quinoline Thiourea-Based Zinc Ionophores with Antibacterial Activity. J. Med. Chem. 66 (16), 11078-11093 https://doi.org/10.1021/acs.jmedchem.3c00368
  • Erol Günal, Ş. (2023). Synthesis Of 2-Fluorobenzoyl Thiourea Derivatives. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi, 22(44), 417-424. https://doi.org/10.55071/ticaretfbd.1364818
  • Hroch L., Guest P., Benek O., Soukup O., Janockova J., Dolezal R., Kuca K., Aitken L., Smith T.K., Gunn-Moore F., Zala D., Ramsay R.R., Musilek K. (2017). Synthesis and evaluation of frentizole-based indolyl thiourea analogues as MAO/ABAD inhibitors for Alzheimer’s disease treatment. Bioorg. Med. Chem. 25(3), 1143-1152. https://doi.org/10.1016/j.bmc.2016.12.029
  • Potts R.O., Guy R.H. (1992). Predicting skin permeability, Pharm. Res. 9, 663–669 https://doi.org/10.1023/a:1015810312465
  • Riccardo, R., Giada, M., Andrea, C., Antimo, G., Emidio, C. (2021). Recent advances in urea- and thiourea-containing compounds: Focus on innovative approaches in medicinal chemistry and organic synthesis. RSC Med. Chem. 12(7), 1046–1064. https://doi.org/10.1039/D1MD00058F
  • Seo, H., Kohlbrand, A.J., Stokes, R.W., Chung, J., Cohen, S.M. (2023). Masking thiol reactivity with thioamide, thiourea, and thiocarbamate-based MBPs. Chem. Commun. 59(16), 2283– 2286. https://doi.org/10.1039/D2CC06596G
  • Shivakumara, K.N., Sridhar, B.T. (2021). Review on role of urea and thiourea derivatives of some heterocyclic Scaffold in drug design and medicinal chemistry. Int. J. Chem. Res. Dev. 3(1), 20–25. https://doi.org/10.33545/26646552.2021.v3.i1a.23
  • Shulgau Z., Palamarchuk I., Sergazy S., Urazbayeva A., Gulyayev A., Ramankulov Y., Kulakov. I. (2024). Synthesis, Computational Study, and In Vitro α-Glucosidase Inhibitory Action of Thiourea Derivatives Based on 3-Aminopyridin-2(1H)-Ones. Molecules. 29(15), 3627. https://doi.org/10.3390/molecules29153627
  • Strzyga-Łach, P., Chrzanowska, A., Podsadni, K., Bielenica, A. (2021). Investigation of the Mechanisms of Cytotoxic Activity of 1,3-Disubstituted Thiourea Derivatives. Pharmaceuticals, 14, 1097. https://doi.org/10.3390/ph14111097
  • Yaqeen, M.A. Rafid, H.A. (2023). Synthesis, Anti-breast Cancer Activity, and Molecular Docking Studies of Thiourea Benzamide Derivatives and Their Complexes with Copper Ion. Trop. J. Nat. Prod. Res. 7(6), 3158–3167. http://www.doi.org/10.26538/tjnpr/v7i6.15
There are 17 citations in total.

Details

Primary Language English
Subjects Organic Chemical Synthesis
Journal Section Research Article
Authors

Şule Erol Günal 0000-0002-2820-7674

Engin Kaplan 0000-0001-5705-717X

Early Pub Date June 14, 2025
Publication Date June 30, 2025
Submission Date November 20, 2024
Acceptance Date March 18, 2025
Published in Issue Year 2025 Volume: 24 Issue: 47

Cite

APA Erol Günal, Ş., & Kaplan, E. (2025). SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi, 24(47), 217-228. https://doi.org/10.55071/ticaretfbd.1588118
AMA Erol Günal Ş, Kaplan E. SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi. June 2025;24(47):217-228. doi:10.55071/ticaretfbd.1588118
Chicago Erol Günal, Şule, and Engin Kaplan. “SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES”. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi 24, no. 47 (June 2025): 217-28. https://doi.org/10.55071/ticaretfbd.1588118.
EndNote Erol Günal Ş, Kaplan E (June 1, 2025) SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi 24 47 217–228.
IEEE Ş. Erol Günal and E. Kaplan, “SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES”, İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi, vol. 24, no. 47, pp. 217–228, 2025, doi: 10.55071/ticaretfbd.1588118.
ISNAD Erol Günal, Şule - Kaplan, Engin. “SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES”. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi 24/47 (June 2025), 217-228. https://doi.org/10.55071/ticaretfbd.1588118.
JAMA Erol Günal Ş, Kaplan E. SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi. 2025;24:217–228.
MLA Erol Günal, Şule and Engin Kaplan. “SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES”. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi, vol. 24, no. 47, 2025, pp. 217-28, doi:10.55071/ticaretfbd.1588118.
Vancouver Erol Günal Ş, Kaplan E. SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES. İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi. 2025;24(47):217-28.