Abstract
Quinoxaline and its derivatives exhibit a broad spectrum of biological activity, making them valuable for various therapeutic applications. However, most quinoxalines are synthetically produced due to their scarcity in nature. In this article, a series of unsymmetric benzils were synthesized and subsequently condensed with 1,2-diaminobenzene to produce unsymmetric quinoxalines. The novel synthetic benzils and quinoxalines were evaluated for their anticancer activities against human non-small-cell lung cancer (NSCLC) cells harboring different gene mutations, to explore their potential as anticancer agents. Among these synthesized molecules, compound 5 g demonstrated inhibitory effects comparable to those of cisplatin.
| Original language | English |
|---|---|
| Article number | e202400847 |
| Pages (from-to) | e202400847 |
| Journal | ChemMedChem |
| Volume | 20 |
| Issue number | 6 |
| Early online date | 26 11 2024 |
| DOIs | |
| State | E-pub ahead of print - 26 11 2024 |
Bibliographical note
© 2024 Wiley-VCH GmbH.Keywords
- Anticancer activities
- Sonogarshira reaction
- Unsymmetric benzil
- Unsymmetric quinoxaline