Redox properties of the iron complexes of orally active iron chelators CP20, CP502, CP509, and ICL670

Helvetica Chimica Acta

Volumn 87, Issue 12, 2004, Pages 3021-3034

  Merkofer, Martin ^a   Kissner, Reinhard ^a   Hider, Robert C ^b   Koppenol, Willem H ^a  

^a LABORATORY OF INORGANIC CHEMISTRY   (Switzerland)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHELATION; CYCLIC VOLTAMMETRY; ELECTRODES; HYDROGEN PEROXIDE; MOLECULAR WEIGHT; OXIDATION; PH EFFECTS; REDOX REACTIONS; STOICHIOMETRY; TOXICITY;

ELECTRODE POTENTIAL; IRON CHELATORS; IRON TOXICITY; REDOX CYCLING;

IRON;

1,4 DIHYDRO 3 HYDROXY N,1,6 TRIMETHYL 4 OXOBENZOIC ACID; 1,4 DIHYDRO 3 HYDROXY N,N,1,6 TETRAMETHYL 4 OXOBENZOIC ACID; BENZOIC ACID DERIVATIVE; CHELATING AGENT; CP 502; CP 509; DEFERASIROX; DEFERIPRONE; HYDROGEN PEROXIDE; HYDROXYL RADICAL; IRON COMPLEX; LIGAND; MERCURY; OXYGEN; PYRIDONE DERIVATIVE; SUPEROXIDE; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CYCLIC POTENTIOMETRY; ELECTRIC POTENTIAL; FENTON REACTION; IRON OVERLOAD; OXIDATION REDUCTION REACTION; PH; PRIORITY JOURNAL; STOICHIOMETRY;

EID: 11244303641     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200490272     Document Type: Article

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