Design, synthesis and biological evaluation of novel anti-cytokine 1,2,4-triazine derivatives

被引:67
|
作者
Khoshneviszadeh, Mehdi [1 ,2 ,3 ]
Ghahremani, Mohammad H. [4 ,5 ]
Foroumadi, Alireza [1 ,2 ,6 ]
Miri, Ramin [3 ]
Firuzi, Omidreza [3 ]
Madadkar-Sobhani, Armin [7 ]
Edraki, Najmeh [1 ,2 ,3 ]
Parsa, Maliheh [4 ]
Shafiee, Abbas [1 ,2 ]
机构
[1] Univ Tehran Med Sci, Dept Med Chem, Fac Pharm, Tehran 14176, Iran
[2] Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14176, Iran
[3] Shiraz Univ Med Sci, Med & Nat Prod Chem Res Ctr, Shiraz, Iran
[4] Univ Tehran Med Sci, Sch Pharm, Dept Pharmacol & Toxicol, Tehran 14176, Iran
[5] Univ Tehran Med Sci, Toxicol & Poisoning Res Ctr, Tehran 14176, Iran
[6] Kerman Univ Med Sci, Neurosci Res Ctr, Kerman, Iran
[7] Univ Tehran, Inst Biochem & Biophys, Tehran, Iran
基金
美国国家科学基金会;
关键词
IL-1; beta; TNF-alpha; p38; MAPK; 1,2,4-Triazine; Anti-inflammatory activity; P38 MAP KINASE; ACTIVATED PROTEIN-KINASE; ANTIINFLAMMATORY ACTIVITY; ANALGESIC ACTIVITY; INHIBITORS; BIOACTIVITIES; POTENT; ACID; RAT;
D O I
10.1016/j.bmc.2013.08.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of 16 novel 1,2,4-triazine derivatives bearing hydrazone moiety (7a-7p) have been designed, synthesized and evaluated for their activity to inhibit IL-1 beta and TNF-alpha production. All compounds are reported for the first time. The chemical structures of all compounds were confirmed by spectroscopic methods and elemental analyzes. Most of the synthesized compounds were proved to have potent anti-cytokine activity and low toxicity on PBMC and MCF-7 cell lines. Compounds 7f, 7k, 7l and 7j presented simultaneously good levels of inhibition of both cytokines. Moreover, compound 7l exhibited good anti-inflammatory effect in carrageenan-induced rat paw edema. The results of Western blotting demonstrated that the anti-cytokine potential of compound 7l is mainly mediated through the inhibition of p38 MAPK signaling pathway. Molecular docking was performed to position compound 7l into p38 alpha binding site in order to explore the potential target. The information of this work might be helpful for the design and synthesis of novel scaffold toward the development of new therapeutic agent to fight against inflammatory diseases. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6708 / 6717
页数:10
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