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4-(4-Fluoro-phen-yl)-2-methyl-3-(1-oxy-4-pyridyl)isoxazol-5(2H)-one.
Acta Crystallogr Sect E Struct Rep Online. 2008 Jan 23;64(Pt 2):o504. doi: 10.1107/S1600536807066500.
Acta Crystallogr Sect E Struct Rep Online. 2008.
PMID: 21201524
Free PMC article.
Fine-tuned PEGylation of chitosan to maintain optimal siRNA-nanoplex bioactivity.
Guţoaia A, Schuster L, Margutti S, Laufer S, Schlosshauer B, Krastev R, Stoll D, Hartmann H.
Guţoaia A, et al. Among authors: margutti s.
Carbohydr Polym. 2016 Jun 5;143:25-34. doi: 10.1016/j.carbpol.2016.01.010. Epub 2016 Jan 8.
Carbohydr Polym. 2016.
PMID: 27083340
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Are MAP kinases drug targets? Yes, but difficult ones.
Margutti S, Laufer SA.
Margutti S, et al.
ChemMedChem. 2007 Aug;2(8):1116-40. doi: 10.1002/cmdc.200600271.
ChemMedChem. 2007.
PMID: 17541990
Review.
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Isoxazolone based inhibitors of p38 MAP kinases.
Laufer SA, Margutti S.
Laufer SA, et al. Among authors: margutti s.
J Med Chem. 2008 Apr 24;51(8):2580-4. doi: 10.1021/jm701343f. Epub 2008 Mar 29.
J Med Chem. 2008.
PMID: 18373337
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Substituted isoxazoles as potent inhibitors of p38 MAP kinase.
Laufer SA, Margutti S, Fritz MD.
Laufer SA, et al. Among authors: margutti s.
ChemMedChem. 2006 Feb;1(2):197-207. doi: 10.1002/cmdc.200500025.
ChemMedChem. 2006.
PMID: 16892352
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4-[4-(4-Fluoro-phen-yl)-2-methyl-5-oxo-2,5-dihydro-isoxazol-3-yl]-1-methyl-pyridinium iodide-4-[3-(4-fluoro-phen-yl)-2-methyl-5-oxo-2,5-dihydro-isoxazol-4-yl]-1-methyl-pyridinium iodide (0.6/0.4).
Margutti S, Schollmeyer D, Laufer S.
Margutti S, et al.
Acta Crystallogr Sect E Struct Rep Online. 2007 Dec 18;64(Pt 1):o298-9. doi: 10.1107/S1600536807055985.
Acta Crystallogr Sect E Struct Rep Online. 2007.
PMID: 21200862
Free PMC article.
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