In the face of bacterial hazards to human health and resistance to multiple antibiotics, there is an urgent need to develop new antibiotics to meet the challenge. In this paper, the triazolyl heterocyclic (3-amino-1,2,4-triazole, ) was synthesised efficiently using thiourea as starting material. Finally, the end product was obtained by aldehyde-amine condensation reaction and the structures of all compounds were determined by spectral analysis. antimicrobial activity showed that had a MIC of 32 μg/mL against the tested and 16 μg/mL against the tested strain. Meanwhile, has a good anti-biofilm effect. Antibacterial mechanism studies have shown that has a good membrane targeting ability, thus disrupting cell membranes, leading to leakage of intracellular proteins and DNA and accelerating bacterial death. In terms of anti-inflammation, dose-dependently inhibits the levels of inflammatory factors NO and IL-6, which deserves further exploration in the treatment of asthma. The study of metal ion removal capacity showed that the synthesised triazole derivatives have high capacity to remove heavy metals Pb, Cd, Ca, Mg, Fe,Cr and Al in the range of 42%-60%.
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http://dx.doi.org/10.3389/fchem.2025.1545259 | DOI Listing |
Front Chem
February 2025
Department of Pediatrics, Maternity and Child Health Hospital of Qinhuangdao, Qinhuangdao, China.
In the face of bacterial hazards to human health and resistance to multiple antibiotics, there is an urgent need to develop new antibiotics to meet the challenge. In this paper, the triazolyl heterocyclic (3-amino-1,2,4-triazole, ) was synthesised efficiently using thiourea as starting material. Finally, the end product was obtained by aldehyde-amine condensation reaction and the structures of all compounds were determined by spectral analysis.
View Article and Find Full Text PDFClin Transl Sci
March 2025
Department of Biostatistics, Yale University School of Public Health, New Haven, Connecticut, USA.
Previous epidemiological studies have suggested that green tea catechins, including Epigallocatechin-3-gallate (EGCG), the most abundant polyphenol in green tea, may be associated with reduced serum folate levels. This is of particular interest as women of childbearing age may be consuming EGCG from tea, dietary supplements, or involved in active clinical trials studying EGCG or green tea extract. EGCG was reported to shrink uterine fibroids in preclinical and clinical studies.
View Article and Find Full Text PDFBioorg Med Chem Lett
March 2025
Department of Chemistry, Birla Institute of Technology and Science, Pilani, Hyderabad Campus, Jawahar Nagar, Kapra Mandal, Hyderabad 500078, Telangana, India. Electronic address:
In this work, novel 2-substituted-3-((1-substituted-1H-1,2,3-triazol-4-yl) methoxy) quinoxaline analogues were designed, synthesized, and various analytical techniques, viz., H NMR, C NMR, and Mass spectrometry, were deployed in the structure confirmation of the final compounds. Synthesized derivatives were evaluated for their antimycobacterial activity against Mycobacterium tuberculosis (Mtb) H37Rv.
View Article and Find Full Text PDFNeurochem Int
March 2025
Department of Anesthesiology, Pain and Perioperative Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China. Electronic address:
Chemotherapy-induced peripheral neuropathy (CIPN) severely diminishes the quality of life for cancer survivors, yet effective treatments remain scarce. Esketamine, a commonly used anesthetic, has demonstrated neuroprotective effects by restoring gut microbiome dysbiosis. In this study, we investigated the impact of esketamine on nociceptive sensitivity in a mouse model of CIPN and explored the potential involvement of the gut microbiome.
View Article and Find Full Text PDFTurk J Pharm Sci
March 2025
Ege University Faculty of Pharmacy, Department of Pharmaceutical Chemistry, İzmir, Türkiye.
Objectives: Excessive amounts of neuroapoptosis are the underlying cause of neurodegenerative diseases. Bax is a pro-apoptotic member of the B-cell lymphoma-2 family that activates caspases which are the members of the cysteine protease family that play a significant role in the initiation and execution phases of apoptosis. The aim of this study was to design and synthesize a group of N-propananilide derivatives bearing pyrazole or 1,2,4-triazole ring were designed and synthesized to analyze the neuroprotectivity potential against 6-hydroxy-dopamine (6-OHDA).
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