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3-hydroxypyridin-4-one

Known as: HP-4-one 
National Institutes of Health

Papers overview

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2018
2018
Depriving microorganisms of bioavailable iron is a promising strategy for new anti-infective agents. The new, highly water… 
2012
2012
As an aid in optimising the design of 3-hydroxypyridin-4-ones (HPOs) intended for use as therapeutic Fe(3+) chelating agents… 
2008
2008
Iron overload is a critical clinical problem that can be prevented by the use of iron-specific chelating agents. An alternative… 
2001
2001
The structural and physiochemical properties of 3-hydroxypyridin-4-one chelators (HPOs) which influence inhibition of the iron… 
1994
1994
Clinical trials of 1,2-dimethyl-3-hydroxypyridine-4-one (1) as an orally available iron chelator are presently underway in… 
1993
1993
The effects of 3-hydroxypyridin-4-one (HPO) iron chelators and desferrioxamine (DFO) on murine hemopoiesis in vivo and in vitro… 
Highly Cited
1992
Highly Cited
1992
The effect of bidentate 3-hydroxypyridin-4-one (HPO) iron chelators on cell cycle arrest with subsequent cycle synchronization… 
Highly Cited
1991
Highly Cited
1991
Five orally effective iron chelators of the 3-hydroxypyridin-4-one series have been administered intraperitoneally to iron… 
Highly Cited
1991
Highly Cited
1991
The ability of 3-hydroxypyridin-4-ones (CP), a family of bidentate orally effective iron chelators, to remove iron and to prevent… 
Highly Cited
1991
Highly Cited
1991
The antimalaria effect of iron chelators is attributed to their interaction with a labile iron pool within parasitised…