174355-17-0Relevant articles and documents
Synthesis and antiviral evaluation of 3-hydroxy-2-methylpyridin-4-one dideoxynucleoside derivatives
Barral, Karine,Hider, Robert C.,Balzarini, Jan,Neyts, Johan,De Clercq, Erik,Camplo, Michel
, p. 4371 - 4374 (2003)
We describe the synthesis and the antiviral evaluation of novel α and β dideoxynucleoside derivatives in which the base has been replaced by a 3-hydroxy-2-methylpyridin-4-one. The syntheses were successfully achieved by the use of the standard Vorbrueggen coupling conditions. Moderate activity of these compounds were found on herpes simplex virus (HSV) type 1 and type 2.
Compositions and methods for chelation therapy
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Page/Page column 16, (2010/02/15)
The invention relates to compositions and methods of treatment using an iron chelator, an antioxidant, estrogen, and/or combinations thereof, optionally, linked to a nanoparticle, to treat a subject in need thereof. The compositions and methods may be used to restore or protect the normal functions of osteoblast and osteoclast by depleting iron and inhibiting oxidative damage. The compositions and methods may also be used to increase the bone formation rate in a subject.
Efficient synthesis of N-[(2-hydroxyethoxy) methyl]-2-alkyl-3-hydroxy-4-pyridinone by a modified Hilbert-Johnson reaction
Liu, Gang,Miller, Scott C.,Bruenger, Fred W.
, p. 2681 - 2686 (2007/10/03)
Ethyleneglycol derivatives of 2-methyl (and ethyl)-3-hydroxy-4-pyridinone were synthesized by a modified Hilbert-Johnson reaction. The synthesis proceeds by reaction of O-protected 2-alkyl-3-hydroxy-4-pyridinone with hexamethyldisilazane in the presence o
Synthesis of 2-alkyl-3-hydroxy-4-pyridinone-ribonucleosides, potential oral iron chelators
Liu,Bruenger,Barrios,Miller
, p. 1901 - 1904 (2007/10/02)
Several ribonucleosides, named 2-alkyl-3-hydroxy-1-(β-D-ribofuranosyl or pyranosyl)-4-pyridinones, were synthesized in good yield. The method provides a useful means to obtain α-ketohydroxypyridin derivatives with different sugar moieties that, if used as