Meggio F - Search Results

1

Identification of ellagic acid as potent inhibitor of protein kinase CK2: a successful example of a virtual screening application.

Cozza G, Bonvini P, Zorzi E, Poletto G, Pagano MA, Sarno S, Donella-Deana A, Zagotto G, Rosolen A, Pinna LA, Meggio F, Moro S. Cozza G, et al. Among authors: meggio f. J Med Chem. 2006 Apr 20;49(8):2363-6. doi: 10.1021/jm060112m. J Med Chem. 2006. PMID: 16610779

2

One-thousand-and-one substrates of protein kinase CK2?

Meggio F, Pinna LA. Meggio F, et al. FASEB J. 2003 Mar;17(3):349-68. doi: 10.1096/fj.02-0473rev. FASEB J. 2003. PMID: 12631575 Review.

3

Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA).

Sarno S, de Moliner E, Ruzzene M, Pagano MA, Battistutta R, Bain J, Fabbro D, Schoepfer J, Elliott M, Furet P, Meggio F, Zanotti G, Pinna LA. Sarno S, et al. Among authors: meggio f. Biochem J. 2003 Sep 15;374(Pt 3):639-46. doi: 10.1042/BJ20030674. Biochem J. 2003. PMID: 12816539 Free PMC article.

4

2-Dimethylamino-4,5,6,7-tetrabromo-1H-benzimidazole: a novel powerful and selective inhibitor of protein kinase CK2.

Pagano MA, Meggio F, Ruzzene M, Andrzejewska M, Kazimierczuk Z, Pinna LA. Pagano MA, et al. Among authors: meggio f. Biochem Biophys Res Commun. 2004 Sep 3;321(4):1040-4. doi: 10.1016/j.bbrc.2004.07.067. Biochem Biophys Res Commun. 2004. PMID: 15358133

5

Inhibition of protein kinase CK2 by condensed polyphenolic derivatives. An in vitro and in vivo study.

Meggio F, Pagano MA, Moro S, Zagotto G, Ruzzene M, Sarno S, Cozza G, Bain J, Elliott M, Deana AD, Brunati AM, Pinna LA. Meggio F, et al. Biochemistry. 2004 Oct 12;43(40):12931-6. doi: 10.1021/bi048999g. Biochemistry. 2004. PMID: 15461466 Free article.

6

Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole.

Pagano MA, Andrzejewska M, Ruzzene M, Sarno S, Cesaro L, Bain J, Elliott M, Meggio F, Kazimierczuk Z, Pinna LA. Pagano MA, et al. Among authors: meggio f. J Med Chem. 2004 Dec 2;47(25):6239-47. doi: 10.1021/jm049854a. J Med Chem. 2004. PMID: 15566294

7

Autophosphorylation at the regulatory beta subunit reflects the supramolecular organization of protein kinase CK2.

Pagano MA, Sarno S, Poletto G, Cozza G, Pinna LA, Meggio F. Pagano MA, et al. Among authors: meggio f. Mol Cell Biochem. 2005 Jun;274(1-2):23-9. doi: 10.1007/s11010-005-3116-y. Mol Cell Biochem. 2005. PMID: 16335525

8

Development and exploitation of CK2 inhibitors.

Sarno S, Ruzzene M, Frascella P, Pagano MA, Meggio F, Zambon A, Mazzorana M, Di Maira G, Lucchini V, Pinna LA. Sarno S, et al. Among authors: meggio f. Mol Cell Biochem. 2005 Jun;274(1-2):69-76. doi: 10.1007/s11010-005-3079-z. Mol Cell Biochem. 2005. PMID: 16335530

9

Discrimination between the activity of protein kinase CK2 holoenzyme and its catalytic subunits.

Salvi M, Sarno S, Marin O, Meggio F, Itarte E, Pinna LA. Salvi M, et al. Among authors: meggio f. FEBS Lett. 2006 Jul 10;580(16):3948-52. doi: 10.1016/j.febslet.2006.06.031. Epub 2006 Jun 21. FEBS Lett. 2006. PMID: 16806200 Free article.

10

Tetrabromocinnamic acid (TBCA) and related compounds represent a new class of specific protein kinase CK2 inhibitors.

Pagano MA, Poletto G, Di Maira G, Cozza G, Ruzzene M, Sarno S, Bain J, Elliott M, Moro S, Zagotto G, Meggio F, Pinna LA. Pagano MA, et al. Among authors: meggio f. Chembiochem. 2007 Jan 2;8(1):129-39. doi: 10.1002/cbic.200600293. Chembiochem. 2007. PMID: 17133643

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