Efficient Scavenging of Superoxide Radical (02-) in Vitro and In Vivo.

Abstract

We have prepared manganic porphyrins, as mimics of SOD activity. Several generalizations follow: (a) In vivo action may involve cycles of reduction by NAD(P)H, or GSH, and reoxidation by O2; whereas the in vitro cycle involves O2 in both reduction and oxidation steps. (b) Action of mimics on bacterial cells is only a rough indicator of their action on mammalian cells; because of differences in uptake of the compounds. (c) Redox potential is more important than net charge, for activity in the in vitro assay. The most active compound we have prepared to date is the Mn(III) 2,3,7,8,12,13,17, 18-octabromo-5, 10, 15,20-tetrakis (N-methyl pyridinium-4-yl)porphyrin. Since the electron withdrawing effect of Br<Cl<F, we will also explore the synthesis and properties of the octachloro and octafluoro analogues. Bromination increased the rate constant by -50-fold. Chlorination or fluorination might provide even greater improvements.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1996
Accession Number
ADA323481

Entities

People

  • Irwin Fridovich

Organizations

  • Duke University Hospital

Tags

DTIC Thesaurus Topics

  • Analogs
  • Biomedical Research
  • Bromination
  • Cells
  • Chemical Compounds
  • Chemical Reaction Properties
  • Chemical Synthesis
  • Chemistry
  • Chlorination
  • Electrons
  • Fluorination
  • Halogenation
  • Hemorrhagic Shock
  • North Carolina
  • Porphyrins
  • Superoxides
  • Vascular Diseases

Fields of Study

  • Chemistry

Readers

  • Molecular and Cellular Biochemistry
  • Organic Chemistry

Technology Areas

  • Microelectronics