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
相关论文
共 50 条
  • [41] Synthesis of naphthyridin-2(1H)-one derivatives via ring expansion of 3-substituted-1H-pyrrolo[2,3-b]pyridin-2(3H)-one derivatives
    Croix, C.
    Massip, S.
    Viaud-Massuard, M. -C.
    CHEMICAL COMMUNICATIONS, 2018, 54 (44) : 5538 - 5541
  • [42] ANTIBACTERIAL AND CENTRAL NERVOUS SYSTEM ACTIVITY OF (4,5-DIARYL-4H-1,2,4-TRIAZOL-3-YL)METHACRYLIC ACID DERIVATIVES
    Paprocka, Renata
    Modzelewska-Banachiewicz, Bozena
    Kutkowska, Jolanta
    Pawlowski, Kamil
    Piatkowska-Chmiel, Iwona
    Jagiello-Wojtowicz, Ewa
    ACTA POLONIAE PHARMACEUTICA, 2017, 74 (01): : 289 - 292
  • [43] Synthesis and Biological Evaluation of 3,6-diaryl-7H-thiazolo[3,2-b] [1,2,4]triazin-7-one Derivatives as Acetylcholinesterase Inhibitors
    Jin, Zhe
    Yang, Liu
    Liu, Si-Jie
    Wang, Jian
    Li, Shuo
    Lin, Huang-Quan
    Wan, David Chi Cheong
    Hu, Chun
    ARCHIVES OF PHARMACAL RESEARCH, 2010, 33 (10) : 1641 - 1649
  • [44] Synthesis, biological evaluation and molecular modeling study of new (1,2,4-triazole or 1,3,4-thiadiazole)-methylthio-derivatives of quinazolin-4(3H)-one as DHFR inhibitors
    El-Gazzar, Yomna I.
    Georgey, Hanan H.
    El-Messery, Shahenda M.
    Ewida, Heba A.
    Hassan, Ghada S.
    Raafat, Marwa M.
    Ewida, Menna A.
    El-Subbagh, Hussein I.
    BIOORGANIC CHEMISTRY, 2017, 72 : 282 - 292
  • [45] Synthesis of 3-Aminopyridin-2(1H)-Ones and 1H-Pyrido[2,3-b][1,4]Oxazin-2(3H)-Ones
    Fisyuk, A. S.
    Kulakov, I. V.
    Goncharov, D. S.
    Nikitina, O. S.
    Bogza, Y. P.
    Shatsauskas, A. L.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2014, 50 (02) : 217 - 224
  • [46] S-substituted 2-mercaptoquinazolin-4(3H)-one and 4-ethylbenzensulfonamides act as potent and selective human carbonic anhydrase IX and XII inhibitors
    El-Azab, Adel S.
    Abdel-Aziz, Alaa A. -M.
    Bua, Silvia
    Nocentini, Alessio
    AlSaif, Nawaf A.
    Alanazi, Mohammed M.
    El-Gendy, Manal A.
    Ahmed, Hany E. A.
    Supuran, Claudiu T.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2020, 35 (01) : 733 - 743
  • [47] Synthesis, biological activities, and SAR studies of novel 1-(2-chloro-4,5-difluorophenyl)-1H-pyyrazole derivatives
    Zhao, Yangyang
    Li, Huangong
    Sun, Pengwei
    Gao, Li
    Liu, Jingbo
    Zhou, Sha
    Xiong, Lixia
    Yang, Na
    Li, Yuxin
    Li, Zhengming
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2020, 30 (22)
  • [48] Synthesis, biological evaluation, and in silico study of novel library sulfonates containing quinazolin-4(3H)-one derivatives as potential aldose reductase inhibitors
    Tokali, Feyzi Sinan
    Demir, Yeliz
    Demircioglu, Ibrahim Hakki
    Turkes, Cuneyt
    Kalay, Erbay
    Sendil, Kivilcim
    Beydemir, Sukru
    DRUG DEVELOPMENT RESEARCH, 2022, 83 (03) : 586 - 604
  • [49] Modified Salicylanilide and 3-Phenyl-2H-benzo[e][1,3]oxazine-2,4(3H)-dione Derivatives as Novel Inhibitors of Osteoclast Differentiation and Bone Resorption
    Chen, Chun-Liang
    Liu, Fei-Lan
    Lee, Chia-Chung
    Chen, Tsung-Chih
    Ali, Ahmed Atef Ahmed
    Sytwu, Huey-Kang
    Chang, Deh-Ming
    Huang, Hsu-Shan
    JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (19) : 8072 - 8085
  • [50] Synthesis and Antitumor Evaluation of Novel 5-Hydrosulfonyl-1H-benzo[d]imidazol-2(3H)-one Derivatives
    Ouyang, Guang
    Tong, Rongsheng
    Li, Jinqi
    Bai, Lan
    Ouyang, Liang
    Duan, Xingmei
    Li, Fengqiong
    He, Pin
    Shi, Jianyou
    He, Yuxin
    MOLECULES, 2016, 21 (04)