Synthesis, characterization and anti-tumor activity of novel thymoquinone analogs against pancreatic cancer

被引:38
|
作者
Yusufi, Mujahid [1 ]
Banerjee, Sanjeev [2 ]
Mohammad, Momin [3 ]
Khatal, Sandhya [4 ]
Swamy, K. Venkateswara [4 ]
Khan, Ejazuddin M. [1 ]
Aboukameel, Amro [2 ]
Sarkar, Fazlul H. [2 ,3 ]
Padhye, Subhash [1 ,2 ]
机构
[1] Univ Pune, Abeda Inamdar Coll, Dept Chem, ISTRA, Pune 411001, Maharashtra, India
[2] Wayne State Univ, Sch Med, Dept Pathol, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Oncol, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[4] Dr DY Patil Vidyapeeth, Dr DY Patil Biotechnol & Bioinformat Inst, Dept Bioinformat & Comp Sci, Pune 411044, Maharashtra, India
关键词
Thymoquinone analogs; Molecular Docking; Pancreatic cancer; Thymoquinone; Chemosensitisation; Gemcitabine; PHASE-II TRIAL; SCHIFF-BASES; CELLS; CYCLOOXYGENASE-2; INHIBITORS; CELECOXIB; LIPOXYGENASE; GEMCITABINE; EXPRESSION; PREVENTION;
D O I
10.1016/j.bmcl.2013.03.003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Thymoquinone (TQ), isolated from the seeds of Nigella sativa, show moderate efficacy against pancreatic cancer. In the present work we report synthesis and characterization of novel TQ analogs appended with gallate and fluorogallate pharmacophores and evaluation of their effects against pancreatic cancer cell lines for cell viability and induction of apoptosis. The efficacy of the analogs alone or in combination with Gemcitabine was assessed in vitro. LC-MS spectra of ATQTHB and ATQTFB showed major peaks corresponding to expected M+1 fragment at 316.34 and 322.34 respectively. Molecular docking studies revealed good fit for these analogs in the COX-2 protein cavity with better binding energies compared to parent TQ compound. Present TQ analogs exhibit superior anti-proliferative activity, excellent chemo-sensitizing activity against pancreatic cancer in vitro and in combination with Gemcitabine. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3101 / 3104
页数:4
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