Literature DB >> 9784102

Design of new topoisomerase II inhibitors based upon a quinobenzoxazine self-assembly model.

Q Zeng1, Y Kwok, S M Kerwin, G Mangold, L H Hurley.   

Abstract

A new class of pyridobenzophenoxazine compounds has been developed as topoisomerase II inhibitors for anticancer chemotherapy. These compounds were designed based on a proposed model of a quinobenzoxazine self-assembly complex on DNA. They showed excellent inhibitory effects on several tumor cell lines with nanomolar IC50 values. Their cytotoxic potency correlates with their ability to unwind DNA and inhibit topoisomerase II.

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Year:  1998        PMID: 9784102     DOI: 10.1021/jm980265c

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Charge state-dependent fragmentation of oligonucleotide/metal complexes.

Authors:  Karin M Keller; Jennifer S Brodbelt
Journal:  J Am Soc Mass Spectrom       Date:  2005-01       Impact factor: 3.109

Review 2.  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

3.  Synthesis, evaluation, and CoMFA study of fluoroquinophenoxazine derivatives as bacterial topoisomerase IA inhibitors.

Authors:  Xufen Yu; Mingming Zhang; Thirunavukkarasu Annamalai; Priyanka Bansod; Gagandeep Narula; Yuk-Ching Tse-Dinh; Dianqing Sun
Journal:  Eur J Med Chem       Date:  2016-09-18       Impact factor: 6.514

  3 in total

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