Synthesis and anticancer activities of thiosemicarbazones derivatives of thiochromanones and related scaffolds

被引:0
作者
Jiangli Song
Rongkai Pan
Guobi Li
Wenyi Su
Xiumei Song
Jincheng Li
Shenggui Liu
机构
[1] Lingnan Normal University,School of Chemistry & Chemical Engineering
[2] Key Laboratory of Clean Energy Materials Chemistry of Guangdong Higher Education Institute,Industrial Technology Research Institute
[3] Lingnan Normal University,undefined
来源
Medicinal Chemistry Research | 2020年 / 29卷
关键词
Thiosemicarbazone; Thiochromanone; Benzothiazepine; Cytotoxic activity; Apoptosis;
D O I
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中图分类号
学科分类号
摘要
A series of novel thiosemicarbazone analogs (4a–t, 6a–j) were synthesized and evaluated for their cytotoxic activities. The obtained results showed that thiochromanone-based thiosemicarbazones substituted primarily at the C-8 position exhibited higher cytotoxicity than the corresponding 1,1-dioxo-thiochromanone-, benzothiazepine-, and 1,1-dioxo-benzothiazepine-based analogs. Significantly, compound 4c (8-fluoro thiochromanone thiosemicarbazone) was found to be the most active and exhibited potent cytotoxicity against the MCF-7, SK-mel-2, and DU145 cancer cell lines, with IC50 values of 0.42, 0.58, and 0.43 µM, respectively. In addition, the mechanism of compound 4c induced MCF-7 cell apoptosis was preliminarily investigated through cell cycle, Annexin V-FITC/PI staining, and ROS assays, indicating that compound 4c may exert its anticancer property through ROS-mediated apoptosis.
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页码:630 / 642
页数:12
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[31]  
Cheng Z(2011)Novel chelators for cancer treatment: where are we now? Nat Rev Clin Oncol 8 6974-18
[32]  
Wang Y(2015)Preclinical development of molecular-targeted agents for cancer Bioorg Med Chem 23 359-542
[33]  
Chavarria GE(2018)Synthesis and biochemical evaluation of benzoylbenzophenone thiosemicarbazone analogues as potent and selective inhibitors of cathepsin L Eur J Med Chem 144 12-100
[34]  
Horsman MR(2016)Multifunctional thiosemicarbazones and deconstructed analogues as a strategy to study the involvement of metal chelation, Sigma-2 (σ2) receptor and P-gp protein in the cytotoxic action: in vitro and in vivo activity in pancreatic tumors Facta Universitatis Ser: Med Biol 18 531-133
[35]  
Arispe WM(2008)Biochemical and molecular mechanisms of action of cisplatin in cancer cells Nat Clin Pr Oncol 5 91-812
[36]  
Kumar GDK(2018)The role of hormonal therapy in the management of hormonal-receptor-positive breast cancer with co-expression of HER2 Eur J Med Chem 154 119-453
[37]  
Chen SE(2004)Synthesis, antiproliferative activity and mechanism of gallium(III)-thiosemicarbazone complexes as potential anti-breast cancer agents Coord Chem Rev 248 805-2807
[38]  
Strecker TE(2011)Contribution to the SAR field of metallated and coordination complexes: studies of the palladium and platinum derivatives with selected thiosemicarbazones as antitumoral drugs Nat Rev Cancer 11 338-188
[39]  
Parker EN(2017)Novel cancer immunotherapy agents with survival benefit: recent successes and next steps Front Cell Neurosci 11 450-1028
[40]  
Chaplin DJ(2012)Mechanisms of cisplatin-induced ototoxicity and otoprotection ACS Med Chem Lett 3 2801-8