Calderone V - Search Results

1

Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1/L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands.

Primofiore G, Taliani S, Da Settimo F, Marini AM, La Motta C, Simorini F, Patrizi MP, Sergianni V, Novellino E, Greco G, Cosimelli B, Calderone V, Montali M, Besnard F, Martini C. Primofiore G, et al. Among authors: calderone v. J Med Chem. 2007 Apr 5;50(7):1627-34. doi: 10.1021/jm0607707. Epub 2007 Mar 3. J Med Chem. 2007. PMID: 17335185

2

5-(4'-Substituted-2'-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. I.

Biagi G, Calderone V, Giorgi I, Livi O, Scartoni V, Baragatti B, Martinotti E. Biagi G, et al. Among authors: calderone v. Eur J Med Chem. 2000 Jul-Aug;35(7-8):715-20. doi: 10.1016/s0223-5234(00)00180-x. Eur J Med Chem. 2000. PMID: 10960187

3

Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2, 3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2, 3-b]pyridine:potential antihypertensive agents - part IX.

Ferrarini PL, Mori C, Badawneh M, Calderone V, Greco R, Manera C, Martinelli A, Nieri P, Saccomanni G. Ferrarini PL, et al. Among authors: calderone v. Eur J Med Chem. 2000 Sep;35(9):815-26. doi: 10.1016/s0223-5234(00)00173-2. Eur J Med Chem. 2000. PMID: 11006483

4

Triazolyl-benzimidazolones and triazolyl-benzotriazoles: new potential potassium channel activators. II.

Baragatti B, Biagi G, Calderone V, Giorgi I, Livi O, Martinotti E, Scartoni V. Baragatti B, et al. Among authors: calderone v. Eur J Med Chem. 2000 Oct;35(10):949-55. doi: 10.1016/s0223-5234(00)01170-3. Eur J Med Chem. 2000. PMID: 11121621

5

Conformationally restrained analogues of sympathomimetic catecholamines. Synthesis and adrenergic activity of 5,6- and 6,7-dihydroxy-3,4-dihydrospiro[naphthalen-1(2H)-2',5'-morpholines].

Balsamo A, Lapucci A, Manera C, Martinelli A, Nencetti S, Orlandini E, Calderone V, Giannaccini G, Nieri P. Balsamo A, et al. Among authors: calderone v. Eur J Med Chem. 2002 Jan;37(1):11-22. doi: 10.1016/s0223-5234(01)01322-8. Eur J Med Chem. 2002. PMID: 11841871

6

Large-conductance, ca(2+)-activated k(+) channels: function, pharmacology and drugs.

Calderone V. Calderone V. Curr Med Chem. 2002 Jul;9(14):1385-95. doi: 10.2174/0929867023369871. Curr Med Chem. 2002. PMID: 12132994 Review.

7

Highly potent 1,4-benzothiazine derivatives as K(ATP)-channel openers.

Cecchetti V, Calderone V, Tabarrini O, Sabatini S, Filipponi E, Testai L, Spogli R, Martinotti E, Fravolini A. Cecchetti V, et al. Among authors: calderone v. J Med Chem. 2003 Aug 14;46(17):3670-9. doi: 10.1021/jm030791q. J Med Chem. 2003. PMID: 12904071

8

Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: identification of beta 3-antagonists.

Saccomanni G, Badawneh M, Adinolfi B, Calderone V, Cavallini T, Ferrarini PL, Greco R, Manera C, Testai L. Saccomanni G, et al. Among authors: calderone v. Bioorg Med Chem. 2003 Nov 17;11(23):4921-31. doi: 10.1016/j.bmc.2003.09.017. Bioorg Med Chem. 2003. PMID: 14604653

9

Synthesis and biological evaluation of 1,8-naphthyridin-4(1H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors.

Ferrarini PL, Calderone V, Cavallini T, Manera C, Saccomanni G, Pani L, Ruiu S, Gessa GL. Ferrarini PL, et al. Among authors: calderone v. Bioorg Med Chem. 2004 Apr 15;12(8):1921-33. doi: 10.1016/j.bmc.2004.01.035. Bioorg Med Chem. 2004. PMID: 15051060

10

Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V.

Biagi G, Giorgi I, Livi O, Nardi A, Calderone V, Martelli A, Martinotti E, LeRoy Salerni O. Biagi G, et al. Among authors: calderone v. Eur J Med Chem. 2004 Jun;39(6):491-8. doi: 10.1016/j.ejmech.2004.02.006. Eur J Med Chem. 2004. PMID: 15183907

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