Casini A - 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: casini a. 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: sulfonamides incorporating furan-, thiophene- and pyrrole-carboxamido groups possess strong topical intraocular pressure lowering properties as aqueous suspensions.

Ilies M, Supuran CT, Scozzafava A, Casini A, Mincione F, Menabuoni L, Caproiu MT, Maganu M, Banciu MD. Ilies M, et al. Among authors: casini a. Bioorg Med Chem. 2000 Aug;8(8):2145-55. doi: 10.1016/s0968-0896(00)00143-7. Bioorg Med Chem. 2000. PMID: 11003159

3

Carbonic anhydrase inhibitors: water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects.

Casini A, Scozzafava A, Mincione F, Menabuoni L, Ilies MA, Supuran CT. Casini A, et al. J Med Chem. 2000 Dec 14;43(25):4884-92. doi: 10.1021/jm001051+. J Med Chem. 2000. PMID: 11123998

4

Carbonic anhydrase inhibitors: synthesis and inhibition against isozymes I, II and IV of topically acting antiglaucoma sulfonamides incorporating cis-5-norbornene-endo-3-carboxy-2-carboxamido moieties.

Casini A, Mincione F, Ilies MA, Menabuoni L, Scozzafava A, Supuran CT. Casini A, et al. J Enzyme Inhib. 2001;16(2):113-23. doi: 10.1080/14756360109162361. J Enzyme Inhib. 2001. PMID: 11342280

5

Carbonic anhydrase inhibitors: 4-sulfamoyl-benzenecarboxamides and 4-chloro-3-sulfamoyl-benzenecarboxamides with strong topical antiglaucoma properties.

Mincione F, Starnotti M, Menabuoni L, Scozzafava A, Casini A, Supuran CT. Mincione F, et al. Among authors: casini a. Bioorg Med Chem Lett. 2001 Jul 9;11(13):1787-91. doi: 10.1016/s0960-894x(01)00303-1. Bioorg Med Chem Lett. 2001. PMID: 11425561

6

Targeting cysteine residues of biomolecules: new approaches for the design of antiviral and anticancer drugs.

Scozzafava A, Casini A, Supuran CT. Scozzafava A, et al. Among authors: casini a. Curr Med Chem. 2002 Jun;9(12):1167-85. doi: 10.2174/0929867023370077. Curr Med Chem. 2002. PMID: 12052170 Review.

7

Sulfonamides and sulfonylated derivatives as anticancer agents.

Casini A, Scozzafava A, Mastrolorenzo A, Supuran LT. Casini A, et al. Curr Cancer Drug Targets. 2002 Mar;2(1):55-75. doi: 10.2174/1568009023334060. Curr Cancer Drug Targets. 2002. PMID: 12188921 Review.

8

Cyclodextrin complexes of sulfonamide carbonic anhydrase inhibitors as long-lasting topically acting antiglaucoma agents.

Maestrelli F, Mura P, Casini A, Mincione F, Scozzafava A, Supuran CT. Maestrelli F, et al. Among authors: casini a. J Pharm Sci. 2002 Oct;91(10):2211-9. doi: 10.1002/jps.10215. J Pharm Sci. 2002. PMID: 12226848

9

Carbonic anhydrase inhibitors with strong topical antiglaucoma properties incorporating a 4-(2-aminopyrimidin-4-yl-amino)-benzenesulfonamide scaffold.

Casini A, Mincione F, Vullo D, Menabuoni L, Scozzafava A, Supuran CT. Casini A, et al. J Enzyme Inhib Med Chem. 2002 Feb;17(1):9-18. doi: 10.1080/14756360290018602. J Enzyme Inhib Med Chem. 2002. PMID: 12365464 Free article.

10

Cysteine-modifying agents: a possible approach for effective anticancer and antiviral drugs.

Casini A, Scozzafava A, Supuran CT. Casini A, et al. Environ Health Perspect. 2002 Oct;110 Suppl 5(Suppl 5):801-6. doi: 10.1289/ehp.02110s5801. Environ Health Perspect. 2002. PMID: 12426135 Free PMC article. Review.

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