Recent applications of 1,3-thiazole core structure in the identification of new lead compounds and drug discovery

被引:388
作者
Ayati, Adile [1 ,2 ]
Emami, Saeed [3 ,4 ]
Asadipour, Ali [5 ]
Shafiee, Abbas [1 ,2 ]
Foroumadi, Alireza [1 ,2 ,5 ]
机构
[1] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran, Iran
[2] Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran, Iran
[3] Mazandaran Univ Med Sci, Fac Pharm, Dept Med Chem, Sari, Iran
[4] Mazandaran Univ Med Sci, Fac Pharm, Pharmaceut Sci Res Ctr, Sari, Iran
[5] Kerman Univ Med Sci, Inst Neuropharmacol, Neurosci Res Ctr, Kerman, Iran
基金
美国国家科学基金会;
关键词
Thiazole; Antimicrobials; Anti-cancer; Antioxidants; Anti-inflammatory; Anticonvulsants; Enzyme inhibitors; Lead compounds; BIOLOGICAL EVALUATION; ANTIVIRAL ACTIVITY; 2,4-DISUBSTITUTED THIAZOLES; ANTICONVULSANTS DESIGN; CYTOTOXIC EVALUATION; ANTITUMOR-ACTIVITY; POTENT INHIBITORS; KAPPA-B; DERIVATIVES; ANALOGS;
D O I
10.1016/j.ejmech.2015.04.015
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
1,3-Thiazole is one of the most important scaffolds in heterocyclic chemistry and drug design and discovery. It is widely found in diverse pharmacologically active substances and in some naturally-occurring compounds. Thiazole is a versatile building-block for lead generation, and is easily access of diverse derivatives for subsequent lead optimization. In the recent years, many thiazole derivatives have been synthesized and subjected to varied biological activities. In this article we intended to review the most important biological effects of thiazole-based compounds and highlight their roles in new leads identification and drug discovery. This article is also intended to help researches for finding potential future directions on the development of more potent and specific analogs of thiazole-based compounds for various biological targets. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:699 / 718
页数:20
相关论文
共 142 条
[1]   Synthesis, antimicrobial, antioxidant, anti-hemolytic and cytotoxic evaluation of new imidazole-based heterocycles [J].
Abdel-Wahab, Bakr F. ;
Awad, Ghada E. A. ;
Badria, Farid A. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2011, 46 (05) :1505-1511
[2]  
Abele E., 2007, CHEM HETEROCYCLIC CO
[3]   Synthesis and pharmacological evaluation of some novel 2-(5-hydroxy-5-trifluoromethyl-4,5-dihydropyrazol-1-yl)-4-(coumarin-3-yl)thiazoles [J].
Aggarwal, Ranjana ;
Kumar, Sunil ;
Kaushik, Pawan ;
Kaushik, Dhirender ;
Gupta, Girish Kumar .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 62 :508-514
[4]   1-[(2-Arylthiazol-4-yl)methyl]azoles as a New Class of Anticonvulsants: Design, Synthesis, In vivo Screening, and In silico Drug-like Properties [J].
Ahangar, Nematollah ;
Ayati, Adile ;
Alipour, Eskandar ;
Pashapour, Arsalan ;
Foroumadi, Alireza ;
Emami, Saeed .
CHEMICAL BIOLOGY & DRUG DESIGN, 2011, 78 (05) :844-852
[5]   Synthesis and biological evaluation of 2-phenylthiazole-4-carboxamide derivatives as anticancer agents [J].
Aliabadi, Alireza ;
Shamsa, Fazel ;
Ostad, Seyed Nasser ;
Emami, Saeed ;
Shafiee, Abbas ;
Davoodi, Jamshid ;
Foroumadi, Alireza .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (11) :5384-5389
[6]   Synthesis and preliminary evaluation of some substituted coumarins as anticonvulsant agents [J].
Amin, Kamelia M. ;
Rahman, Doaa E. Abdel ;
Al-Eryani, Yasmin A. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (10) :5377-5388
[7]   Design and synthesis of thiazole-5-hydroxamic acids as novel histone deacetylase inhibitors [J].
Anandan, Sampath-Kumar ;
Ward, John S. ;
Brokx, Richard D. ;
Denny, Trisha ;
Bray, Mark R. ;
Patel, Dinesh V. ;
Xiao, Xiao-Yi .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (21) :5995-5999
[8]  
[Anonymous], FEBS LETT
[9]  
[Anonymous], BIOORG MED CHEM
[10]   Synthesis, spectral and biological evaluation of some new thiazolidinones and thiazoles based on t-3-alkyl-r-2,c-6-diarylpiperidin-4-ones [J].
Aridoss, G. ;
Amirthaganesan, S. ;
Kim, M. S. ;
Kim, J. T. ;
Jeong, Yeon Tae .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (10) :4199-4210