Literature DB >> 10219099

Recent advances in the discovery and development of quinolones and analogs as antitumor agents.

Y Xia1, Z Y Yang, S L Morris-Natschke, K H Lee.   

Abstract

Compounds that interact with DNA or microtubules by multiple mechanisms and cause diverse cytotoxic lesions are potential targets for anticancer drug development. Accordingly, a relatively new approach to the rational design of antitumor agents is based on the quinolone class of antibacterials. Their mechanism of antibacterial action involves inhibition of DNA gyrase, and numerous new quinolones do exhibit antitumor activity. Thus, these new quinolone structures display a novel mode of action for the quinolone class as antitumor agents. The potential for quinolones to be used as topoisomerase II inhibitors, as well as antimitotic agents, is reviewed with a focus on recent discoveries and development of antitumor quinolones, especially related work in the author's laboratory.

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Year:  1999        PMID: 10219099

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


  3 in total

Review 1.  A "Double-Edged" Scaffold: Antitumor Power within the Antibacterial Quinolone.

Authors:  Gregory S Bisacchi; Michael R Hale
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

2.  Interaction of N-methyl-2-alkenyl-4-quinolones with ATP-dependent MurE ligase of Mycobacterium tuberculosis: antibacterial activity, molecular docking and inhibition kinetics.

Authors:  Juan David Guzman; Abraham Wube; Dimitrios Evangelopoulos; Antima Gupta; Antje Hüfner; Chandrakala Basavannacharya; Md Mukhleshur Rahman; Christina Thomaschitz; Rudolf Bauer; Timothy Daniel McHugh; Irene Nobeli; Jose M Prieto; Simon Gibbons; Franz Bucar; Sanjib Bhakta
Journal:  J Antimicrob Chemother       Date:  2011-05-28       Impact factor: 5.790

3.  Novel N-2-(Furyl)-2-(chlorobenzyloxyimino) Ethyl Piperazinyl Quinolones: Synthesis, Cytotoxic Evaluation and Structure-Activity Relationship.

Authors:  Negar Mohammadhosseini; Mahboobeh Pordeli; Maliheh Safavi; Loghman Firoozpour; Fatame Amin; Sussan Kabudanian Ardestani; Najmeh Edraki; Abbas Shafiee; Alireza Foroumadi
Journal:  Iran J Pharm Res       Date:  2015       Impact factor: 1.696

  3 in total

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