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Synthesis and biological evaluation of farnesylthiosalicylamides as potential anti-tumor agents.

Abstract：

:Fourteen hybrids of farnesylthiosalicylic acid (FTS) with various diamines were synthesized and biologically evaluated. It was found that FTS-monoamide molecules (10a-g) displayed strong anti-proliferative activity against seven human cancer cell lines, superior to FTS and FTS-bisamide compounds (11a-g). The mono-amide 10f was the most active, with IC₅₀s of 3.78-7.63 μM against all tested cancer cells, even more potent than sorafenib (9.12-22.9 μM). In addition, 10f induced SMMC-7721 cell apoptosis, down-regulated the expression of Bcl-2 and up-regulated Bax and caspase-3. Furthermore, 10f had the improved aqueous solubility relative to FTS. Finally, treatment with 10f dose-dependently inhibited the Ras-related signaling pathways in SMMC-7721 cells. Collectively, 10f could be a promising candidate for the intervention of human cancers.

journal_name

Bioorg Med Chem

journal_title

Bioorganic & medicinal chemistry

authors

Ling Y,Wang Z,Zhu H,Wang X,Zhang W,Wang X,Chen L,Huang Z,Zhang Y

doi

10.1016/j.bmc.2013.11.013

subject

Has Abstract

pub_date

2014-01-01 00:00:00

pages

374-80

issue

1

eissn

0968-0896

issn

1464-3391

pii

S0968-0896(13)00944-9

journal_volume

22

pub_type

杂志文章

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