DU145型
烯类反应
环加成
催化作用
化学
基质(水族馆)
立体化学
有机化学
癌细胞
癌症
生物
生态学
遗传学
LNCaP公司
作者
Eeda Lingareddy,Aishwarya Nadagouda,Lokavarapu Sai,Todeti Pardha Saradhi,Sudhakar Bansod,Anjana Devi Tangutur,Jagadeesh Babu Nanubolu,Ravindra M. Kumbhare
标识
DOI:10.1002/slct.202402070
摘要
Abstract A series of substituted spiro 4‐thia‐1,2,6,9‐tetraazaspiro[4.4]non‐2‐ene‐7,8‐diones were synthesized with good yields through 1,3‐dipolar substituted hydrazonoylchloride's substituted 2‐thioxoimidazolidin‐4,5‐diones under mild conditions as described. This switchable C−S and C−N bond connection with simple execution and broad substrate scope. In this study, the synthesized compounds 3 a – q were screened against four distinct cancer cell lines (PANC‐1, MIA PaCa‐2, MDA MB231 and DU145) along with a standard cell line HEK‐293 , to determine their in vitro anticancer activities, and assessed using the Sulphorhodamine B assay to determine their viability
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