Synthesis of novel perillyl–dihydropyrimidinone hybrids designed for antiproliferative activity
作者:Vinicius Vendrusculo、Vanessa P. de Souza、Luiz Antônio M. Fontoura、Marcelo G. M. D'Oca、Thais P. Banzato、Paula A. Monteiro、Ronaldo A. Pilli、João Ernesto de Carvalho、Dennis Russowsky
DOI:10.1039/c8md00270c
日期:——
A series of fifteen novel dihydropyrimidinone hybrid compounds were synthesized in good yields via a multicomponent reaction combined with the Huisgen reaction. The antiproliferative activity was investigated against nine tumor cell lines, and four hybrid compounds (TGI < 10 μM) showed promising antiproliferative activity against the tumor cell lines OVCAR-3 (ovarian), UACC-62 (melanoma) and U251 (glioma)
通过多组分反应与Huisgen反应相结合,以良好的收率合成了一系列十五种新型二氢嘧啶酮杂化化合物。针对 9 种肿瘤细胞系进行了抗增殖活性研究,四种混合化合物 (TGI < 10 μM) 对肿瘤细胞系 OVCAR-3(卵巢)、UACC-62(黑色素瘤)和 U251(神经胶质瘤)显示出良好的抗增殖活性。所检测的几种混合化合物对于人类角质形成细胞系 (HaCat) 具有较高的 TGI 值 (TGI 147.92–507.82),这表明对癌细胞具有选择性。