Synthesis, anticancer and antiviral activities of novel thiopyrano[2,3-<i>d</i>]thiazole-6-carbaldehydes
作者:Andrii Lozynskyi、Sergii Golota、Borys Zimenkovsky、Dmytro Atamanyuk、Andrzej Gzella、Roman Lesyk
DOI:10.1080/10426507.2016.1166108
日期:2016.9.1
NCI and AACF protocols. Anticancer activity screening on NCI60 cell lines allowed identification of 7-phenyl-2-oxo-7-phenyl-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazole-6-carbaldehyde 3a with the highest level of antimitotic activity against leukemia with mean GI50/TGI values 1.26/25.22 μM. The screening of antiviral activity lead to identification of 7-(4-methoxyphenyl)-2-oxo-3,5,6,7-tetrahydro-2H-thiopyrano[2
图形摘要 摘要 通过区域合成了新型 rel-(6R,7R)-2-oxo-7-phenyl-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazole-6-carbaldehydes 5-亚芳基-4-硫代-2-噻唑烷酮与丙烯醛的非对映选择性杂-Diels-Alder反应。美国国立卫生研究院 (NIH) 根据美国 NCI 和 AACF 协议对合成化合物的抗癌和抗病毒活性进行了评估。NCI60 细胞系的抗癌活性筛选允许鉴定 7-phenyl-2-oxo-7-phenyl-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazole-6-carbaldehyde 3a最高水平的抗白血病抗有丝分裂活性,平均 GI50/TGI 值为 1.26/25.22 μM。抗病毒活性的筛选导致7-(4-甲氧基苯基)-2-氧代-3,5,6,7-四氢-2H-噻喃[2