The design of orally active iron chelators.

Abstract:

:It is now generally accepted that it is not possible to design iron(III)-selective hexadentate chelators with high oral bioavailability. In order to achieve suitable levels of oral activity for the treatment of systemic iron overload either tridentate or bidentate molecules need to be investigated. There are a number of such molecules in clinical practice, including hydroxypyridin-4-ones, desferrithiocin analogues and bis-hydroxyphenyltriazoles. The underlying chemistry of each group is described, together with an indication of the distribution properties, redox cycling activity, and iron scavenging activity.

journal_name

Ann N Y Acad Sci

authors

Hider RC,Zhou T

doi

10.1196/annals.1345.017

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

141-54

eissn

0077-8923

issn

1749-6632

pii

1054/1/141

journal_volume

1054

pub_type

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