1333391-35-7Relevant articles and documents
Synthesis of novel thiazolyl-pyrimidines and their anticancer activity in vitro
Shi, Hai-Bo,Li, Hai-Bo,Lu, Kong-Qin,Zhu, Xia-Re,Hu, Wei-Xiao,Pei, Wen
, p. 675 - 683 (2012/06/01)
A series of novel compounds 7-43 were prepared via the condensation of enaminones 4a-h and the guanidines carbonate 6a-f. The structures of these newly synthesized compounds were confirmed by 1H-NMR, MS, EA and IR. All the compounds were tested for their cytotoxic activity in vitro against human cancer cell lines including Ishikawa, A549, BEL-7404, SPC-A-01 and SGC-7901. Most of them showed moderate cytotoxic against the tested cell lines. Among them, the most potent compounds 9 and 30 exhibited more efficient activity against Ishikawa, A549. Thiazolyl-pyrimidines were synthesized by the general pyrimidine condensation of Bredereck and their in-vitro anticancer activities were evaluated. Copyright