Mastrolorenzo A - Search Results

1

Molecular cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Malassezia globosa, a potential antidandruff target.

Hewitson KS, Vullo D, Scozzafava A, Mastrolorenzo A, Supuran CT. Hewitson KS, et al. Among authors: mastrolorenzo a. J Med Chem. 2012 Apr 12;55(7):3513-20. doi: 10.1021/jm300203r. Epub 2012 Mar 28. J Med Chem. 2012. PMID: 22424239

2

Carbonic anhydrase inhibitors. Design of selective, membrane-impermeant inhibitors targeting the human tumor-associated isozyme IX.

Casey JR, Morgan PE, Vullo D, Scozzafava A, Mastrolorenzo A, Supuran CT. Casey JR, et al. Among authors: mastrolorenzo a. J Med Chem. 2004 Apr 22;47(9):2337-47. doi: 10.1021/jm031079w. J Med Chem. 2004. PMID: 15084132

3

COX-2 selective inhibitors, carbonic anhydrase inhibition and anticancer properties of sulfonamides belonging to this class of pharmacological agents.

Supuran CT, Casini A, Mastrolorenzo A, Scozzafava A. Supuran CT, et al. Among authors: mastrolorenzo a. Mini Rev Med Chem. 2004 Aug;4(6):625-32. doi: 10.2174/1389557043403792. Mini Rev Med Chem. 2004. PMID: 15279596

4

Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with phosphates, carbamoyl phosphate, and the phosphonate antiviral drug foscarnet.

Rusconi S, Innocenti A, Vullo D, Mastrolorenzo A, Scozzafava A, Supuran CT. Rusconi S, et al. Among authors: mastrolorenzo a. Bioorg Med Chem Lett. 2004 Dec 6;14(23):5763-7. doi: 10.1016/j.bmcl.2004.09.064. Bioorg Med Chem Lett. 2004. PMID: 15501037

5

Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides.

Nishimori I, Vullo D, Innocenti A, Scozzafava A, Mastrolorenzo A, Supuran CT. Nishimori I, et al. Among authors: mastrolorenzo a. Bioorg Med Chem Lett. 2005 Sep 1;15(17):3828-33. doi: 10.1016/j.bmcl.2005.06.055. Bioorg Med Chem Lett. 2005. PMID: 16039848

6

Carbonic anhydrase inhibitors. The mitochondrial isozyme VB as a new target for sulfonamide and sulfamate inhibitors.

Nishimori I, Vullo D, Innocenti A, Scozzafava A, Mastrolorenzo A, Supuran CT. Nishimori I, et al. Among authors: mastrolorenzo a. J Med Chem. 2005 Dec 1;48(24):7860-6. doi: 10.1021/jm050483n. J Med Chem. 2005. PMID: 16302824

7

Carbonic anhydrase inhibitors. Interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: kinetic and X-ray crystallographic studies.

Temperini C, Innocenti A, Mastrolorenzo A, Scozzafava A, Supuran CT. Temperini C, et al. Among authors: mastrolorenzo a. Bioorg Med Chem Lett. 2007 Sep 1;17(17):4866-72. doi: 10.1016/j.bmcl.2007.06.044. Epub 2007 Jun 14. Bioorg Med Chem Lett. 2007. PMID: 17588751

8

Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides.

Güzel O, Maresca A, Hall RA, Scozzafava A, Mastrolorenzo A, Mühlschlegel FA, Supuran CT. Güzel O, et al. Among authors: mastrolorenzo a. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2508-11. doi: 10.1016/j.bmcl.2010.02.103. Epub 2010 Mar 3. Bioorg Med Chem Lett. 2010. PMID: 20299219

9

Carbonic anhydrase inhibitors: inhibition of the β-class enzyme from the pathogenic yeast Candida glabrata with sulfonamides, sulfamates and sulfamides.

Vullo D, Leewattanapasuk W, Mühlschlegel FA, Mastrolorenzo A, Capasso C, Supuran CT. Vullo D, et al. Among authors: mastrolorenzo a. Bioorg Med Chem Lett. 2013 May 1;23(9):2647-52. doi: 10.1016/j.bmcl.2013.02.092. Epub 2013 Mar 1. Bioorg Med Chem Lett. 2013. PMID: 23511020

10

Anticancer and antiviral sulfonamides.

Scozzafava A, Owa T, Mastrolorenzo A, Supuran CT. Scozzafava A, et al. Among authors: mastrolorenzo a. Curr Med Chem. 2003 Jun;10(11):925-53. doi: 10.2174/0929867033457647. Curr Med Chem. 2003. PMID: 12678681 Review.

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