Literature DB >> 15080977

Synthesis and biochemical properties of E-ring modified luotonin A derivatives.

Ali Cagir1, Shannon H Jones, Brian M Eisenhauer, Rong Gao, Sidney M Hecht.   

Abstract

Luotonin A is a cytotoxic pyrroloquinazolinoquinoline alkaloid that has been shown to stabilize the human topoisomerase I-DNA covalent binary complex in the same fashion as the antitumor alkaloid camptothecin. A study of the structural elements in luotonin A required for binary complex stabilization has revealed key differences relative to those required for camptothecin.

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Year:  2004        PMID: 15080977     DOI: 10.1016/j.bmcl.2004.02.069

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  One-pot synthesis of densely functionalized cyclic β-aminoesters containing four stereocenters, based on a Et3N-promoted pseudo five-component reaction.

Authors:  Juan Yao; Lanxiang Zhou; Chen Tan; Cunde Wang
Journal:  Mol Divers       Date:  2014-09-26       Impact factor: 2.943

2.  A theoretical study of some new analogues of the anti-cancer drug camptothecin.

Authors:  Nihar R Jena; Phool C Mishra
Journal:  J Mol Model       Date:  2006-10-06       Impact factor: 1.810

  2 in total

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