Literature DB >> 15670914

Understanding topoisomerase I and II in terms of QSAR.

Rajeshwar P Verma1.   

Abstract

A variety of antitumor agents currently used in chemotherapy or evaluated in clinical trials are known to inhibit DNA topoisomerase I or II. We have developed sixteen quantitative structure-activity relationships (QSAR) for different sets of compounds that are camptothecin analogs, 1,4-naphthoquinones, unsaturated acids, benzimidazoles, quinolones, and miscellaneous fused heterocycles to understand chemical-biological interactions governing their inhibitory activities toward topoisomerase I and II.

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Year:  2005        PMID: 15670914     DOI: 10.1016/j.bmc.2004.11.033

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  2 in total

1.  Diversity-oriented synthesis of benzimidazole, benzoxazole, benzothiazole and quinazolin-4(3H)-one libraries via potassium persulfate-CuSO4-mediated oxidative coupling reactions of aldehydes in aqueous micelles.

Authors:  Atul Kumar; Ram Awatar Maurya; Deepti Saxena
Journal:  Mol Divers       Date:  2009-07-04       Impact factor: 2.943

2.  Microwave-assisted Cu(I)-catalyzed, three-component synthesis of 2-(4-((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-1H-benzo[d]imidazoles.

Authors:  Yogesh Kumar; Vijay Bahadur; Anil Kumar Singh; Virinder Singh Parmar; Erik V Van der Eycken; Brajendra Kumar Singh
Journal:  Beilstein J Org Chem       Date:  2014-06-24       Impact factor: 2.883

  2 in total

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