New Quinazolin-4(3<i>H</i>)-one Derivatives as Potential Antitumoral Compounds: Synthesis, In Vitro Cytotoxicity Against the HepG2 Cell Line, and In Silico VEGFR-2 Targeting-Based Studies
Three new 2,3-disubstituted quinazolin-4(3<i>H</i>)-one derivatives (<b>5a</b>–<b>c</b>) were synthesized by the nucleophilic <i>S</i>-alkylation of 2-mercaptoquinazolin-4(3<i>H</i>)-one derivatives (<b>3a</b>–<b>c</b>) with 5-(2-bromoacetyl)-2-hydroxybenzamide (<b>4</b>) in alkaline conditions. The...
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| Үндсэн зохиолчид: | , , , , , , , , , , , |
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| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
MDPI AG
2025-12-01
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| Цуврал: | Molecules |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://www.mdpi.com/1420-3049/30/24/4719 |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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