Araştırma Makalesi

Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives

Cilt: 11 Sayı: 1 2 Ağustos 2024
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Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives

Öz

In the present study, 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (3c, f, e) reacted with 4-methylthiobenzaldehyde to afford 3-alkyl(aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-ones (4c, f, e). The structures of three new compounds were established from the elemental analysis, IR, 1H NMR, and 13C NMR spectral data. The newly synthesized and recently synthesized 3-alkyl(aryl)-4-(4-methylthiobenzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one derivatives were analyzed using three methods for antioxidant activities. Compound 4a showed the best activity for the metal chelating effect. Furthermore, the compounds' antimicrobial activity was screened.

Anahtar Kelimeler

Destekleyen Kurum

Scientific Research Projects Coordination Unit of Kafkas University

Proje Numarası

2016-FM-61

Etik Beyan

The approval of an ethical committee is not required.

Teşekkür

The authors thank Dr. Muzaffer Alkan for their contribution.

Kaynakça

  1. Abbas, A., Nadeem, H., Khan, A. U., Ali, F., Afzaal, H., Nadhman, A., & Khan, I. (2017). Synthesis, characterization, antioxidant, antimicrobial, cytotoxic, anticancer, leishmanicidal, anti-inflammatory activities and docking studies of heterocyclic 1,3,4-oxadiazoles and 4-amino-1,2,4-triazoles derivatives. Journal of the Chemical Society of Pakistan, 39(4), 661–673.
  2. Aboeldahab, A. M. A., Beshr, E. A. M., Shoman, M. E., Rabea, S. M., & Aly, O. M. (2018). Spirohydantoins and 1,2,4-triazole-3-carboxamide derivatives as inhibitors of histone deacetylase: Design, synthesis, and biological evaluation. European Journal of Medicinal Chemistry, 146, 79–92.
  3. Abuelhassan, A. H., Badran, M. M., Hassan, H. A., Abdelhamed, D., Elnabtity, S., & Aly, O. M. (2018). Design, synthesis, anticonvulsant activity, and pharmacophore study of new 1,5-diaryl-1H-1,2,4-triazole-3-carboxamide derivatives. Medicinal Chemistry Research, 27(3), 928–938.
  4. Ahmad, I., Mehmood, Z., & Mohammad, F. (1998). Screening of some Indian medicinal plants for their antimicrobial properties. Journal of Ethnopharmacology, 62(2), 183–193.
  5. Aktas-Yokus, O., Yuksek, H., Manap, S., Aytemiz, F., Alkan, M., Beytur, M., & Gursoy-Kol, O. (2017). In-vitro biological activity of some new 1,2,4-triazole derivatives with their potentiometric titrations. Bulgarian Chemical Communications, 49(I), 98–106.
  6. Bajpai, V. K., Rather, I. A., & Shukla, S. (2016). Microbes in Food and Health-Oxidative Stress: Role of NaturalAntioxidant Compounds (N. Garg, S. M. Abdel-Aziz, & A. Aeron (eds.)). Springer International Publishing: Switzerland.
  7. Blois, M. (1958). Antioxidant Determinations by the Use of a Stable Free Radical. Nature, 181(4617), 1199–1200.
  8. Dinis, T. C. P., Madeira, V. M. C., & Almeida, L. M. (1994). Action of Phenolic Derivatives (Acetaminophen, Salicylate, and 5-Aminosalicylate) as Inhibitors of Membrane Lipid Peroxidation and as Peroxyl Radical Scavengers. Archives of Biochemistry and Biophysics, 315(1), 161–169. Gupta, V. K., & Sharma, S. K. (2006). Plants as natural antioxidants. Natural Product Radiance, 5(4), 326–334.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Organik Kimyasal Sentez

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

2 Ağustos 2024

Gönderilme Tarihi

15 Mayıs 2024

Kabul Tarihi

29 Temmuz 2024

Yayımlandığı Sayı

Yıl 2024 Cilt: 11 Sayı: 1

Kaynak Göster

APA
Gürsoy Kol, Ö., Aytemiz, F., Manap, S., & Yüksek, H. (2024). Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives. Caucasian Journal of Science, 11(1), 50-57. https://doi.org/10.48138/cjo.1484675
AMA
1.Gürsoy Kol Ö, Aytemiz F, Manap S, Yüksek H. Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives. Caucasian Journal of Science. 2024;11(1):50-57. doi:10.48138/cjo.1484675
Chicago
Gürsoy Kol, Özlem, Fevzi Aytemiz, Sevda Manap, ve Haydar Yüksek. 2024. “Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives”. Caucasian Journal of Science 11 (1): 50-57. https://doi.org/10.48138/cjo.1484675.
EndNote
Gürsoy Kol Ö, Aytemiz F, Manap S, Yüksek H (01 Ağustos 2024) Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives. Caucasian Journal of Science 11 1 50–57.
IEEE
[1]Ö. Gürsoy Kol, F. Aytemiz, S. Manap, ve H. Yüksek, “Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives”, Caucasian Journal of Science, c. 11, sy 1, ss. 50–57, Ağu. 2024, doi: 10.48138/cjo.1484675.
ISNAD
Gürsoy Kol, Özlem - Aytemiz, Fevzi - Manap, Sevda - Yüksek, Haydar. “Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives”. Caucasian Journal of Science 11/1 (01 Ağustos 2024): 50-57. https://doi.org/10.48138/cjo.1484675.
JAMA
1.Gürsoy Kol Ö, Aytemiz F, Manap S, Yüksek H. Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives. Caucasian Journal of Science. 2024;11:50–57.
MLA
Gürsoy Kol, Özlem, vd. “Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives”. Caucasian Journal of Science, c. 11, sy 1, Ağustos 2024, ss. 50-57, doi:10.48138/cjo.1484675.
Vancouver
1.Özlem Gürsoy Kol, Fevzi Aytemiz, Sevda Manap, Haydar Yüksek. Synthesis and Biological Evaluation of 3-Alkyl(Aryl)-4-(4-methylthio-benzylideneamino)-4,5-dihidro-1H-1,2,4-triazol-5-one Derivatives. Caucasian Journal of Science. 01 Ağustos 2024;11(1):50-7. doi:10.48138/cjo.1484675

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