Gagliardi S - Search Results

1

Inhibition of Plasmodium falciparum pH regulation by small molecule indole derivatives results in rapid parasite death.

van Schalkwyk DA, Chan XW, Misiano P, Gagliardi S, Farina C, Saliba KJ. van Schalkwyk DA, et al. Among authors: gagliardi s. Biochem Pharmacol. 2010 May 1;79(9):1291-9. doi: 10.1016/j.bcp.2009.12.025. Epub 2010 Jan 11. Biochem Pharmacol. 2010. PMID: 20067768

2

Selective inhibition of osteoclast vacuolar H(+)-ATPase.

Farina C, Gagliardi S. Farina C, et al. Among authors: gagliardi s. Curr Pharm Des. 2002;8(23):2033-48. doi: 10.2174/1381612023393369. Curr Pharm Des. 2002. PMID: 12171517 Review.

3

Chemistry and structure activity relationships of bafilomycin A1, a potent and selective inhibitor of the vacuolar H+-ATPase.

Gagliardi S, Rees M, Farina C. Gagliardi S, et al. Curr Med Chem. 1999 Dec;6(12):1197-212. Curr Med Chem. 1999. PMID: 10519916 Review.

4

Discovery of a novel antitumor benzolactone enamide class that selectively inhibits mammalian vacuolar-type (H+)-atpases.

Boyd MR, Farina C, Belfiore P, Gagliardi S, Kim JW, Hayakawa Y, Beutler JA, McKee TC, Bowman BJ, Bowman EJ. Boyd MR, et al. Among authors: gagliardi s. J Pharmacol Exp Ther. 2001 Apr;297(1):114-20. J Pharmacol Exp Ther. 2001. PMID: 11259534

5

Synthesis of photoactivable inhibitors of osteoclast vacuolar ATPase.

Biasotti B, Dallavalle S, Merlini L, Farina C, Gagliardi S, Parini C, Belfiore P. Biasotti B, et al. Among authors: gagliardi s. Bioorg Med Chem. 2003 May 15;11(10):2247-54. doi: 10.1016/s0968-0896(03)00106-8. Bioorg Med Chem. 2003. PMID: 12713834

6

Synthesis and structure-activity relationships of bafilomycin A1 derivatives as inhibitors of vacuolar H+-ATPase.

Gagliardi S, Gatti PA, Belfiore P, Zocchetti A, Clarke GD, Farina C. Gagliardi S, et al. J Med Chem. 1998 May 21;41(11):1883-93. doi: 10.1021/jm9707838. J Med Chem. 1998. PMID: 9599238

7

Selective inhibitors of the osteoclast vacuolar proton ATPase as novel bone antiresorptive agents.

Farina C, Gagliardi S. Farina C, et al. Among authors: gagliardi s. Drug Discov Today. 1999 Apr;4(4):163-172. doi: 10.1016/S1359-6446(99)01321-5. Drug Discov Today. 1999. PMID: 10322275

8

Novel bone antiresorptive agents that selectively inhibit the osteoclast V-H+-ATPase.

Farina C, Gagliardi S, Nadler G, Morvan M, Parini C, Belfiore P, Visentin L, Gowen M. Farina C, et al. Among authors: gagliardi s. Farmaco. 2001 Jan-Feb;56(1-2):113-6. doi: 10.1016/s0014-827x(01)01013-8. Farmaco. 2001. PMID: 11347950 Review.

9

(2Z,4E)-5-(5,6-dichloro-2-indolyl)-2-methoxy-N-(1,2,2,6,6- pentamethylpiperidin-4-yl)-2,4-pentadienamide, a novel, potent and selective inhibitor of the osteoclast V-ATPase.

Nadler G, Morvan M, Delimoge I, Belfiore P, Zocchetti A, James I, Zembryki D, Lee-Rycakzewski E, Parini C, Consolandi E, Gagliardi S, Farina C. Nadler G, et al. Among authors: gagliardi s. Bioorg Med Chem Lett. 1998 Dec 15;8(24):3621-6. doi: 10.1016/s0960-894x(98)00660-x. Bioorg Med Chem Lett. 1998. PMID: 9934482

10

5-(5,6-Dichloro-2-indolyl)-2-methoxy-2,4-pentadienamides: novel and selective inhibitors of the vacuolar H+-ATPase of osteoclasts with bone antiresorptive activity.

Gagliardi S, Nadler G, Consolandi E, Parini C, Morvan M, Legave MN, Belfiore P, Zocchetti A, Clarke GD, James I, Nambi P, Gowen M, Farina C. Gagliardi S, et al. J Med Chem. 1998 May 7;41(10):1568-73. doi: 10.1021/jm9800144. J Med Chem. 1998. PMID: 9572882

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