Literature DB >> 16457636

Naturally occurring and synthetic imidazoles: their chemistry and their biological activities.

Lidia De Luca1.   

Abstract

Imidazoles are an important class of heterocycles and include many substances of both biological and chemical interest. They are part of a large number of highly significant biomolecules such as the essential amino acid histidine and related compounds, biotin, and the imidazole alkaloids. Insertion of the imidazole nucleus is an important synthetic strategy in drug discovery. Imidazole drugs have broad applications in many areas of clinical medicine. The imidazoles are a class of antifungal azole derivatives and have a broad spectrum of activities both in vitro and in vivo. The imidazole moiety is also contained in many histaminergic ligands for histamine H1, H2, and H3 receptors. These are currently used as tools in pharmacological studies. The important therapeutic properties of imidazole related drugs have encouraged the medicinal chemists to synthesize and test a large number of novel molecules. Some of these have chemotherapeutic properties, such as for example several FTase inhibitors with an imidazole moiety. Imidazole derivatives have also been shown to have antibacterial activity and recently several P38 MAP Kinase inhibitors and 5-Lipoxygenase inhibitors containing the imidazole moiety have been synthesized. This review reports current progress in the area of new biologically active imidazoles and recently discovered naturally occurring imidazole.

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Year:  2006        PMID: 16457636

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  29 in total

1.  Design of novel antituberculosis compounds using graph-theoretical and substructural approaches.

Authors:  Alejandro Speck Planche; Marcus Tulius Scotti; América García López; Vicente de Paulo Emerenciano; Enrique Molina Pérez; Eugenio Uriarte
Journal:  Mol Divers       Date:  2009-04-02       Impact factor: 2.943

Review 2.  Current advances in the synthesis and biological potencies of tri- and tetra-substituted 1H-imidazoles.

Authors:  Majid M Heravi; Mansoureh Daraie; Vahideh Zadsirjan
Journal:  Mol Divers       Date:  2015-04-12       Impact factor: 2.943

3.  High Throughput Synthesis of 2,3,6-Trisubstituted-5,6-Dihydroimidazo[2,1-b]thiazole Derivatives.

Authors:  Yangmei Li; Marc Giulianotti; Richard A Houghten
Journal:  Tetrahedron Lett       Date:  2011-02-09       Impact factor: 2.415

4.  Nitric Oxide-Mediated Induction of Dispersal in Pseudomonas aeruginosa Biofilms Is Inhibited by Flavohemoglobin Production and Is Enhanced by Imidazole.

Authors:  Xinyi Zhu; Hyun-Suk Oh; Yu Chiu Beverly Ng; Pei Yi Peggy Tang; Nicolas Barraud; Scott A Rice
Journal:  Antimicrob Agents Chemother       Date:  2018-02-23       Impact factor: 5.191

5.  C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition.

Authors:  Jung Min Joo; B Barry Touré; Dalibor Sames
Journal:  J Org Chem       Date:  2010-08-06       Impact factor: 4.354

6.  Identification of 5,6-dihydroimidazo[2,1-b]thiazoles as a new class of antimicrobial agents.

Authors:  Yangmei Li; Nina Bionda; Renee Fleeman; Hongjie Wang; Akihiko Ozawa; Richard A Houghten; Lindsey Shaw
Journal:  Bioorg Med Chem       Date:  2016-09-12       Impact factor: 3.641

7.  Bis(4H-1,2,4-triazol-3-yl)disulfane.

Authors:  Dongsheng Liu; Yaping Xu; Xinfa Li; Shaoming Ying; Wentong Chen
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2007-12-12

8.  Regio- and enantioselective N-allylations of imidazole, benzimidazole, and purine heterocycles catalyzed by single-component metallacyclic iridium complexes.

Authors:  Levi M Stanley; John F Hartwig
Journal:  J Am Chem Soc       Date:  2009-07-01       Impact factor: 15.419

9.  A Van Leusen deprotection-cyclization strategy as a fast entry into two imidazoquinoxaline families.

Authors:  Fabio De Moliner; Christopher Hulme
Journal:  Tetrahedron Lett       Date:  2012-08-24       Impact factor: 2.415

10.  Itraconazole-mediated inhibition of calcium entry into platelet-activating factor-stimulated human neutrophils is due to interference with production of leukotriene B4.

Authors:  H C Steel; G R Tintinger; A J Theron; R Anderson
Journal:  Clin Exp Immunol       Date:  2007-08-07       Impact factor: 4.330

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