Menchise V - Search Results

1

Carbonic anhydrase inhibitors: X-ray crystal structure of a benzenesulfonamide strong CA II and CA IX inhibitor bearing a pentafluorophenylaminothioureido tail in complex with isozyme II.

Di Fiore A, De Simone G, Menchise V, Pedone C, Casini A, Scozzafava A, Supuran CT. Di Fiore A, et al. Among authors: menchise v. Bioorg Med Chem Lett. 2005 Apr 1;15(7):1937-42. doi: 10.1016/j.bmcl.2005.01.086. Bioorg Med Chem Lett. 2005. PMID: 15780637

2

Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studies.

De Simone G, Di Fiore A, Menchise V, Pedone C, Antel J, Casini A, Scozzafava A, Wurl M, Supuran CT. De Simone G, et al. Among authors: menchise v. Bioorg Med Chem Lett. 2005 May 2;15(9):2315-20. doi: 10.1016/j.bmcl.2005.03.032. Bioorg Med Chem Lett. 2005. PMID: 15837316

3

Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme II.

Menchise V, De Simone G, Alterio V, Di Fiore A, Pedone C, Scozzafava A, Supuran CT. Menchise V, et al. J Med Chem. 2005 Sep 8;48(18):5721-7. doi: 10.1021/jm050333c. J Med Chem. 2005. PMID: 16134940

4

Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II.

Menchise V, De Simone G, Di Fiore A, Scozzafava A, Supuran CT. Menchise V, et al. Bioorg Med Chem Lett. 2006 Dec 15;16(24):6204-8. doi: 10.1016/j.bmcl.2006.09.022. Epub 2006 Sep 26. Bioorg Med Chem Lett. 2006. PMID: 17000110

5

Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.

De Simone G, Menchise V, Omaggio S, Pedone C, Scozzafava A, Supuran CT. De Simone G, et al. Among authors: menchise v. Biochemistry. 2003 Aug 5;42(30):9013-21. doi: 10.1021/bi020512l. Biochemistry. 2003. PMID: 12885234

6

A substrate-induced switch in the reaction mechanism of a thermophilic esterase: kinetic evidences and structural basis.

De Simone G, Mandrich L, Menchise V, Giordano V, Febbraio F, Rossi M, Pedone C, Manco G. De Simone G, et al. Among authors: menchise v. J Biol Chem. 2004 Feb 20;279(8):6815-23. doi: 10.1074/jbc.M307738200. Epub 2003 Nov 15. J Biol Chem. 2004. PMID: 14617621 Free article.

7

The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase family.

De Simone G, Menchise V, Alterio V, Mandrich L, Rossi M, Manco G, Pedone C. De Simone G, et al. Among authors: menchise v. J Mol Biol. 2004 Oct 8;343(1):137-46. doi: 10.1016/j.jmb.2004.08.014. J Mol Biol. 2004. PMID: 15381425

8

The crystal structure of a hyper-thermophilic carboxylesterase from the archaeon Archaeoglobus fulgidus.

De Simone G, Menchise V, Manco G, Mandrich L, Sorrentino N, Lang D, Rossi M, Pedone C. De Simone G, et al. Among authors: menchise v. J Mol Biol. 2001 Nov 30;314(3):507-18. doi: 10.1006/jmbi.2001.5152. J Mol Biol. 2001. PMID: 11846563

9

Crystallization and preliminary X-ray diffraction studies of a D-lysine-based chiral PNA-DNA duplex.

Menchise V, De Simone G, Corradini R, Sforza S, Sorrentino N, Romanelli A, Saviano M, Pedone C. Menchise V, et al. Acta Crystallogr D Biol Crystallogr. 2002 Mar;58(Pt 3):553-5. doi: 10.1107/s0907444902001427. Epub 2002 Feb 21. Acta Crystallogr D Biol Crystallogr. 2002. PMID: 11856853 Free article.

10

An integrated structural and computational study of the thermostability of two thioredoxin mutants from Alicyclobacillus acidocaldarius.

Bartolucci S, De Simone G, Galdiero S, Improta R, Menchise V, Pedone C, Pedone E, Saviano M. Bartolucci S, et al. Among authors: menchise v. J Bacteriol. 2003 Jul;185(14):4285-9. doi: 10.1128/JB.185.14.4285-4289.2003. J Bacteriol. 2003. PMID: 12837806 Free PMC article.

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