Literature DB >> 19954979

Reaction of reductively activated mitomycin C with aqueous bicarbonate: Isolation and characterization of an oxazolidinone derivative of cis-1-hydroxy-2,7-diaminomitosene.

Manuel M Paz1.   

Abstract

The reductive activation of mitomycin C in aqueous bicarbonate buffer resulted in the formation of a previously unknown compound, characterized as an oxazolidinone derivative of cis-1-hydroxy-2,7-diaminomitosene. This compound is the result of a cyclization reaction of bicarbonate with the aziridine ring of aziridinomitosene, and was observed at bicarbonate concentrations close to those present in physiological plasma. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19954979     DOI: 10.1016/j.bmcl.2009.11.046

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


  1 in total

1.  Acetone promoted 1,4-migration of an alkoxycarbonyl group on a syn-1,2-diamine.

Authors:  Tanya Napolitano; Shu-Yuan Cheng; Brooke Nielsen; Christopher Choi; William Aguilar; Manuel M Paz; Anne-Marie Sapse; Elise Champeil
Journal:  Tetrahedron Lett       Date:  2017-01-03       Impact factor: 2.415

  1 in total

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