Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1399945 | European Journal of Medicinal Chemistry | 2007 | 9 Pages |
Abstract
A series of 2,4-diarylchromane[4,3-d]-Δ1,9b-1,2,3-thiadiazolines have been synthesized by cyclization of corresponding 2-arylchroman-4-one-arylhydrazones with SOCl2 then treated with alcohol. All the compounds have been tested for their antiproliferative activity in vitro against six human tumor cell lines, and the highly potent derivative 11a exhibited in vivo inhibitory effect on tumor growth. Mechanism research indicated that it is due to 11a that induces DNA fragmentation.
Graphical abstractA series of 2,4-diarylchromane[4,3-d]-Δ1,9b-1,2,3-thiadiazolines were prepared and investigated as anticancer agent.Figure optionsDownload full-size imageDownload as PowerPoint slide
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Huazhou Ying, Yongzhou Hu, Qiaojun He, Runping Li, Bo Yang,