22706-12-3Relevant articles and documents
Synthesis, characterization, antimicrobial, and MOE evaluation of nano 1,2,4-triazole-based Schiff base ligand with some d-block metal ions
Mahmoud, Nessma F.,Abbas, Ashraf A.,Mohamed, Gehad G.
, (2021)
Three new metal complexes of 4-(benzylideneamino)-5-phenyl-4H-1,2,4-triazole-3-thiol ligand (L) and three transition metal ions: Fe (III), Cu (II), and Zn (II) were synthesized and characterized. The ligand derived from 4-amino-5-phenyl-1,2,4-triazole-3-thiol and benzaldehyde was synthesized in a 1:1 molar ratio. All the chelates were characterized by elemental analysis, conductivity measurements, thermal analysis, FT-IR, and 1H-NMR spectroscopy. The IR spectrum revealed that the Schiff base ligand coordinated in a neutral bidentate manner with the metal ions through the azomethine N and thiol S. The thiol group coordinated to the metal ions without proton displacement as confirmed from the 1H NMR spectra. The conductivity data showed the electrolytic nature of the Fe (III) and Cu (II) complexes while the Zn (II) complex was nonelectrolyte. All metal complexes had octahedral structure as depicted by spectral and elemental analyses. The complexes start decomposition at 35°C, and they decomposed in four to five steps. The scanning electron microscope (SEM) analysis confirmed the presence of metal complexes in nanostructure. The 1,2,4-triazole Schiff base ligand (L) and its transition metal complexes have been screened for their antibacterial (Gram [+] bacteria): Bacillis subtilis and Staphylococcus aureus, (Gram [?] bacteria): Escherichia coli and Pseudomonas aeruginosa and two fungi: Candida albicans and Aspergillus flavus by agar diffusion method. The two metal complexes were subjected to molecular docking study against crystal structure of Aspergillus fumigatus (PDB ID: 6NE0) and crystal structure of Mycobacterium tuberculosis (PDB ID: 5UHF). The mode of binding between the A. fumigatus (PDB ID: 6NE0) and Mycobacterium tuberculosis strains and the complexes was discussed.
Impact of inclusion complex formation on antibacterial, antioxidant and anthelmintic activities of some 4-arylidenamino-5-phenyl-4H-1,2,4-triazole-3-thiols
Nayak, Sashikanta,Panda, Sunakar
, p. 1144 - 1150 (2017/04/28)
Three different 4-arylidenamino-5-phenyl-4H-l,2,4-triazole-3-thiols have been synthesized and their inclusion complexes are prepared with β-cyclodextrin. The compounds and their inclusion complexes have been characterized by studying their physical and spectral properties. The determination of thermodynamic stability constant and standard free energy change indicates that inclusion complexes of the newly synthesized compounds are stable and their formation is thermodynamically allowed. Finally, the compounds and their inclusion complexes are screened for antibacterial, antioxidant and anthelmintic activities. It is found that inclusion complex formation increases the antibacterial, antioxidant and anthelmintic activities significantly as compared to naked compounds. The higher pharmacological activities have been explained in terms of enhanced solubility in the systemic circulation which makes them more available to specific tissues for better therapeutic efficacy.
Antibacterial, antioxidant and anthelmintic studies of inclusion complexes of some 4-arylidenamino-5-phenyl-4H-1,2,4-triazole-3-thiols
Panda, Sunakar,Nayak, Sashikanta
, p. 679 - 689 (2015/11/03)
A series of 4-arylidenamino-5-phenyl-4H-1,2,4-triazole-3-thiols have been synthesised and their inclusion complexes have been prepared with β-cyclodextrin. The compounds and their inclusion complexes have been characterised by studying their physical and
