Synthesis and SAR study of 4,5-diaryl-1H-imidazole-2(3H)-thione derivatives, as potent 15-lipoxygenase inhibitors

被引:27
|
作者
Assadieskandar, Amir [1 ,2 ]
Amini, Mohsen [1 ,2 ]
Salehi, Marjan [1 ,2 ]
Sadeghian, Hamid [3 ,4 ]
Alimardani, Maliheh [4 ]
Sakhteman, Amirhossein [5 ]
Nadri, Hamid [5 ]
Shafiee, Abbas [1 ,6 ]
机构
[1] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 14176, Iran
[2] Univ Tehran Med Sci, Drug Design & Dev Res Ctr, Tehran 14176, Iran
[3] Mashhad Univ Med Sci, Buali Res Inst, Microbiol & Virol Res Ctr, Mashhad, Iran
[4] Mashhad Univ Med Sci, Sch Paramed Sci, Dept Lab Sci, Mashhad, Iran
[5] Shahid Sadoughi Univ Med Sci, Fac Pharm, Dept Med Chem, Yazd, Iran
[6] Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14176, Iran
关键词
Soybean 15-lipoxygenase (SLO); Radical scavenging activity; Structure-activity relationship studies; 4,5-Diarylimidazole; 3-DIMENSIONAL STRUCTURE; LIPOXYGENASE; DESIGN; EXPRESSION; ATHEROSCLEROSIS; BENZOINS; COX-2;
D O I
10.1016/j.bmc.2012.09.050
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 4,5-diaryl-1H-imidazole-2(3H)-thione was synthesized and their inhibitory potency against soybean 15-lipoxygenase and free radical scavenging activities were determined. Compound 11 showed the best IC50 for 15-LOX inhibition (IC50 = 4.7 mu M) and free radical scavenging activity (IC50 = 14 mu M). Methylation of SH at C-2 position of imidazole has dramatically decreased the 15-LOX inhibition and radical scavenging activity as it can be observed in the inactive compound 14 (IC50 >250 mu M). Structure activity similarity (SAS) showed that the most important chemical modification in this series was methylation of SH group and Docking studies revealed a proper orientation for SH group towards Fe core of the 15-LOX active site. Therefore it was concluded that iron chelating could be a possible mechanism for enzyme inhibition in this series of compounds. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7160 / 7166
页数:7
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