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作为强大的VEGFR-2抑制剂的新型本齐米达-氧迪亚衍生物:合成,抗癌评估和对接研究

Ulviye Acar Çevik1, Ismail Celik2, Şennur Görgülü3

  • 1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.

Drug development research
|June 3, 2024
PubMed
概括

新的本齐米达-氧迪亚衍生物通过抑制血管内皮生长因子受体-2 (VEGFR-2) 来表现出强烈的抗癌活性. 化合物4c表现出卓越的疗效和安全性,突出其作为新型癌症治疗剂的潜力.

关键词:
一个MTTTT,一个MTTTT.在VEGFR-2的基础上.班齐米达的使用情况细胞毒性 细胞毒性分子对接的分子对接.氧沙醇是一种氧沙醇.

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