Isatin-1,2,3-triazole derivatives: synthesis, molecular docking and evaluation against acute experimental toxoplasmosis DOI
Fadwa M. Arafa, Nehal Nassef Hezema, Ateyatallah Aljuhani

и другие.

Acta Tropica, Год журнала: 2024, Номер 260, С. 107471 - 107471

Опубликована: Ноя. 13, 2024

Язык: Английский

Synthesis and X-ray evaluation of 7 N-1S thiabendazole based 1,2,3-triazole as a dual metal sensing probe: Molecular logic gate construction, DFT analysis, real water sample analysis and catalytic activity investigation of its metal complexes DOI
Gurjaspreet Singh,

Tsering Diskit,

Akshpreet Singh

и другие.

Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy, Год журнала: 2025, Номер 330, С. 125737 - 125737

Опубликована: Янв. 10, 2025

Язык: Английский

Процитировано

1

Therapeutic potential of chalcone-1,2,3-triazole hybrids as anti-tumour agents: a systematic review and SAR studies DOI
Sakshi Priya, Md. Shafiqul Islam,

Shivani Kasana

и другие.

Future Medicinal Chemistry, Год журнала: 2025, Номер 17(4), С. 449 - 465

Опубликована: Янв. 31, 2025

The study of chalcone-1,2,3-triazole hybrids for anticancer activity is quite a recent area focus, primarily because the increasing demand developing new drugs to treat cancer. chalcones and 1,2,3-triazole rings in hybrid compounds has recently emerged as promising strategy novel agents. ring, known its stability hydrogen bonding capabilities, enhances target binding affinity these hybrids. Chalcones possess an α,β-unsaturated carbonyl system crucial their synergistic effect two moieties results with potent properties. This review explores structure-activity relationship studies which revealed that electronic lipophilic properties substituents on phenyl significantly influence activity. Electron-donating electron-withdrawing groups can affect cellular uptake engagement. Incorporating various into ring improve selectivity potency against specific cancer cell lines. These often exert effects through apoptosis cycle disruption. Recent research indicates chalcone hold therapeutic promise Further optimization SAR in-depth mechanistic investigations could lead development highly selective agents minimal toxicity.

Язык: Английский

Процитировано

0

Synthesis and antimicrobial activity of benzoxazine/benzothiazine appended 1,2,3-triazole hybrids DOI
Priyanka Yadav, C. P. Kaushik, Devinder Kumar

и другие.

Journal of Molecular Structure, Год журнала: 2024, Номер unknown, С. 140029 - 140029

Опубликована: Сен. 1, 2024

Язык: Английский

Процитировано

2

Progress and challenges in the development of triazole antimicrobials DOI Creative Commons

Muneeb Ur Rehman,

Sihui Long

Future Medicinal Chemistry, Год журнала: 2024, Номер unknown, С. 1 - 3

Опубликована: Ноя. 19, 2024

Язык: Английский

Процитировано

2

Design and synthesis of some novel bis N-[(1,3-dihydro)–2H-indol-2-one]benzidine-1,2,3-triazole hybrids via click chemistry for removing phenanthrene from the aquatic environment DOI
Tamer El Malah, Mahmoud S. Abdel‐Wahed, Ahmed H. Shamroukh

и другие.

Journal of Molecular Liquids, Год журнала: 2024, Номер 406, С. 125088 - 125088

Опубликована: Май 23, 2024

Язык: Английский

Процитировано

1

In-silico screening of Staphylococcus aureus antibacterial agents based on Isatin scaffold: QSAR, molecular docking, molecular dynamics simulation and DFT analysis DOI
Leila Emami, Sara Sadeghian,

Pegah Mardaneh

и другие.

Molecular Physics, Год журнала: 2024, Номер unknown

Опубликована: Сен. 9, 2024

Язык: Английский

Процитировано

0

Isatin-1,2,3-triazole derivatives: synthesis, molecular docking and evaluation against acute experimental toxoplasmosis DOI
Fadwa M. Arafa, Nehal Nassef Hezema, Ateyatallah Aljuhani

и другие.

Acta Tropica, Год журнала: 2024, Номер 260, С. 107471 - 107471

Опубликована: Ноя. 13, 2024

Язык: Английский

Процитировано

0