Current development of 1, 2, 3-triazole derived potential antimalarial scaffolds: Structure activity relationship (SAR) and bioactive compounds

SMA Rahman, JS Bhatti, S Thareja, V Monga - European Journal of …, 2023 - Elsevier
Malaria is among one of the most devastating and deadliest parasitic disease in the world
claiming millions of lives every year around the globe. It is a mosquito-borne infectious …

The antibacterial activity of 1, 2, 3-triazole-and 1, 2, 4-triazole-containing hybrids against Staphylococcus aureus: An updated review (2020-present)

J Li, J Zhang - Current Topics in Medicinal Chemistry, 2022 - ingentaconnect.com
Staphylococcus aureus (S. aureus), a prominent, highly contagious nosocomial and
community-acquired bacterial pathogen, can cause a broad spectrum of diseases. Antibiotic …

Aloe emodin-conjugated sulfonyl hydrazones as novel type of antibacterial modulators against S. aureus 25923 through multifaceted synergistic effects

Z Deng, RRY Bheemanaboina, Y Luo, CH Zhou - Bioorganic Chemistry, 2022 - Elsevier
Aloe emodin-conjugated sulfonyl hydrazones were designed and synthesized as novel type
of antibacterial modulators. Aloe emodin benzenesulfonyl hydrazone 5a (AEBH-5a) was …

Synthesis of benzimidazole-1, 2, 4-triazole derivatives as potential antifungal agents targeting 14α-demethylase

E Guzel, U Acar Çevik, AE Evren, HE Bostancı… - ACS …, 2023 - ACS Publications
Invasive fungal infections (IFIs) are increasing as major infectious diseases around the
world, and the limited efficacy of existing medications has resulted in substantial morbidity …

Antifungal Activity, Structure‐Activity Relationship and Molecular Docking Studies of 1, 2, 4‐Triazole Schiff Base Derivatives

Y Dong, M Li, Y Hao, Y Feng, Y Ren… - Chemistry & …, 2023 - Wiley Online Library
Fourteen novel Schiff base compounds (AS‐1∼ AS‐14) containing 5‐amino‐1H‐1, 2, 4‐
triazole‐3‐carboxylic acid and substituted benzaldehyde were successfully synthesized …

Recent developments in the synthesis of hybrid heterocycles, a promising approach to develop multi-target antibacterial agents

KU Sadek, RA Mekheimer, M Abd-Elmonem… - Journal of Molecular …, 2023 - Elsevier
Hybrid molecules have become a well-established and powerful biologically relevant
heterocycles. They constitute a core structure due to their widespread use in pharmaceutical …

Design, synthesis, antibacterial evaluations and in silico studies of novel thiosemicarbazides and 1, 3, 4-thiadiazoles

S Janowska, D Khylyuk, S Andrzejczuk, M Wujec - Molecules, 2022 - mdpi.com
The emergence of drug-resistant bacterial strains continues to be one of the major
challenges of medicine. For this reason, the importance of searching for novel structures of …

A Review on Chemistry and Methods of Synthesis of 1, 2, 4‐Triazole Derivatives

S Couto Rodrigues… - The Chemical …, 2024 - Wiley Online Library
This review provides a comprehensive overview of research on 1, 2, 4‐triazoles conducted
over the last fifteen years. 1, 2, 4‐Triazoles are highly significant in the pharmaceutical …

Advances in the application of 1, 2, 4-triazole-containing hybrids as anti-tuberculosis agents

Y Cao, H Lu - Future Medicinal Chemistry, 2021 - Taylor & Francis
Tuberculosis is a deadly communicable disease caused by the bacillus Mycobacterium
tuberculosis (MTB), and pulmonary tuberculosis accounts for over 80% of the total cases …

[HTML][HTML] Piperazine-derived small molecules as potential Flaviviridae NS3 protease inhibitors. In vitro antiviral activity evaluation against Zika and Dengue viruses

M del Rosario García-Lozano, F Dragoni, P Gallego… - Bioorganic …, 2023 - Elsevier
Abstract Since 2011 Direct Acting antivirals (DAAs) drugs targeting different non-structural
(NS) viral proteins (NS3, NS5A or NS5B inhibitors) have been approved for clinical use in …