Innocenti A - Search Results

1

Promiscuity of carbonic anhydrase II. Unexpected ester hydrolysis of carbohydrate-based sulfamate inhibitors.

Lopez M, Vu H, Wang CK, Wolf MG, Groenhof G, Innocenti A, Supuran CT, Poulsen SA. Lopez M, et al. Among authors: innocenti a. J Am Chem Soc. 2011 Nov 16;133(45):18452-62. doi: 10.1021/ja207855c. Epub 2011 Oct 19. J Am Chem Soc. 2011. PMID: 21958118

2

A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing".

Wilkinson BL, Bornaghi LF, Houston TA, Innocenti A, Supuran CT, Poulsen SA. Wilkinson BL, et al. Among authors: innocenti a. J Med Chem. 2006 Nov 2;49(22):6539-48. doi: 10.1021/jm060967z. J Med Chem. 2006. PMID: 17064072 Free article.

3

Inhibition of membrane-associated carbonic anhydrase isozymes IX, XII and XIV with a library of glycoconjugate benzenesulfonamides.

Wilkinson BL, Bornaghi LF, Houston TA, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Wilkinson BL, et al. Among authors: innocenti a. Bioorg Med Chem Lett. 2007 Feb 15;17(4):987-92. doi: 10.1016/j.bmcl.2006.11.046. Epub 2006 Nov 17. Bioorg Med Chem Lett. 2007. PMID: 17157501 Free article.

4

Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides.

Wilkinson BL, Bornaghi LF, Houston TA, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Wilkinson BL, et al. Among authors: innocenti a. J Med Chem. 2007 Apr 5;50(7):1651-7. doi: 10.1021/jm061320h. Epub 2007 Mar 8. J Med Chem. 2007. PMID: 17343373

5

Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety.

Salmon AJ, Williams ML, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Salmon AJ, et al. Among authors: innocenti a. Bioorg Med Chem Lett. 2007 Sep 15;17(18):5032-5. doi: 10.1016/j.bmcl.2007.07.024. Epub 2007 Jul 19. Bioorg Med Chem Lett. 2007. PMID: 17681760

6

Inhibition of carbonic anhydrases with glycosyltriazole benzene sulfonamides.

Wilkinson BL, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Wilkinson BL, et al. Among authors: innocenti a. J Med Chem. 2008 Mar 27;51(6):1945-53. doi: 10.1021/jm701426t. Epub 2008 Feb 29. J Med Chem. 2008. PMID: 18307288

7

Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives.

Poulsen SA, Wilkinson BL, Innocenti A, Vullo D, Supuran CT. Poulsen SA, et al. Among authors: innocenti a. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4624-7. doi: 10.1016/j.bmcl.2008.07.010. Epub 2008 Jul 10. Bioorg Med Chem Lett. 2008. PMID: 18644716

8

Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties.

Singer M, Lopez M, Bornaghi LF, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Singer M, et al. Among authors: innocenti a. Bioorg Med Chem Lett. 2009 Apr 15;19(8):2273-6. doi: 10.1016/j.bmcl.2009.02.086. Epub 2009 Feb 26. Bioorg Med Chem Lett. 2009. PMID: 19286378 Free article.

9

Novel organometallic cationic ruthenium(II) pentamethylcyclopentadienyl benzenesulfonamide complexes targeted to inhibit carbonic anhydrase.

Loughrey BT, Williams ML, Healy PC, Innocenti A, Vullo D, Supuran CT, Parsons PG, Poulsen SA. Loughrey BT, et al. Among authors: innocenti a. J Biol Inorg Chem. 2009 Aug;14(6):935-45. doi: 10.1007/s00775-009-0506-8. Epub 2009 Apr 24. J Biol Inorg Chem. 2009. PMID: 19390880

10

S-glycosyl primary sulfonamides--a new structural class for selective inhibition of cancer-associated carbonic anhydrases.

Lopez M, Paul B, Hofmann A, Morizzi J, Wu QK, Charman SA, Innocenti A, Vullo D, Supuran CT, Poulsen SA. Lopez M, et al. Among authors: innocenti a. J Med Chem. 2009 Oct 22;52(20):6421-32. doi: 10.1021/jm900914e. J Med Chem. 2009. PMID: 19827837

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