Literature DB >> 25934508

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

Adile Ayati1, Saeed Emami2, Ali Asadipour3, Abbas Shafiee1, Alireza Foroumadi4.   

Abstract

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.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Anti-cancer; Anti-inflammatory; Anticonvulsants; Antimicrobials; Antioxidants; Enzyme inhibitors; Lead compounds; Thiazole

Mesh:

Substances:

Year:  2015        PMID: 25934508     DOI: 10.1016/j.ejmech.2015.04.015

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  34 in total

1.  2-(3'-Indolyl)-N-arylthiazole-4-carboxamides: Synthesis and evaluation of antibacterial and anticancer activities.

Authors:  Mukund P Tantak; Jing Wang; Rajnish Prakash Singh; Anil Kumar; Kavita Shah; Dalip Kumar
Journal:  Bioorg Med Chem Lett       Date:  2015-08-06       Impact factor: 2.823

Review 2.  Synthesis of Biologically Active Molecules through Multicomponent Reactions.

Authors:  Daniel Insuasty; Juan Castillo; Diana Becerra; Hugo Rojas; Rodrigo Abonia
Journal:  Molecules       Date:  2020-01-24       Impact factor: 4.411

3.  Importance of substituents in ring opening: a DFT study on a model reaction of thiazole to thioamide.

Authors:  Xue Bai; Dan Qin; Lijun Yang
Journal:  J Mol Model       Date:  2021-02-21       Impact factor: 1.810

Review 4.  Thiazole Ring-A Biologically Active Scaffold.

Authors:  Anthi Petrou; Maria Fesatidou; Athina Geronikaki
Journal:  Molecules       Date:  2021-05-25       Impact factor: 4.411

5.  Synthesis and biological evaluation of aminothiazoles against Histoplasma capsulatum and Cryptococcus neoformans.

Authors:  Keisuke Ishita; Stavros Stefanopoulos; Ahmed Khalil; Xiaolin Cheng; Werner Tjarks; Chad A Rappleye
Journal:  Bioorg Med Chem       Date:  2018-02-02       Impact factor: 3.641

6.  Benign Synthesis of Fused-thiazoles with Enone-based Natural Products and Drugs for Lead Discovery.

Authors:  Rawan Alnufaie; Mohamad Akbar Ali; Ibrahim S Alkhaibari; Subrata Roy; Victor W Day; Mohammad A Alam
Journal:  New J Chem       Date:  2021-03-02       Impact factor: 3.591

7.  Thiazole-Based Thiosemicarbazones: Synthesis, Cytotoxicity Evaluation and Molecular Docking Study.

Authors:  Sobhi M Gomha; Hyam A Abdelhady; Doaa Z H Hassain; Aboubakr H Abdelmonsef; Mohamed El-Naggar; Mahmoud M Elaasser; Huda K Mahmoud
Journal:  Drug Des Devel Ther       Date:  2021-02-17       Impact factor: 4.162

8.  Synthesis of Chimeric Thiazolo-Nootkatone Derivatives as Potent Antimicrobial Agents.

Authors:  Ibrahim S Alkhaibari; Hansa Raj K C; Rawan Alnufaie; David Gilmore; Mohammad A Alam
Journal:  ChemMedChem       Date:  2021-06-09       Impact factor: 3.466

9.  Meloxicam methyl group determines enzyme specificity for thiazole bioactivation compared to sudoxicam.

Authors:  Dustyn A Barnette; Mary A Schleiff; Arghya Datta; Noah Flynn; S Joshua Swamidass; Grover P Miller
Journal:  Toxicol Lett       Date:  2020-11-27       Impact factor: 4.372

10.  Sulfur-containing therapeutics in the treatment of Alzheimer's disease.

Authors:  Haizhou Zhu; Venkateshwara Dronamraju; Wei Xie; Swati S More
Journal:  Med Chem Res       Date:  2021-01-15       Impact factor: 1.965

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.