Castellano S - Search Results

1

A new class of antifungal agents. Synthesis and antimycotic activity of disubstituted N-azolylamines.

Castellano S, Stefancich G, Musiu C, La Colla P. Castellano S, et al. Arch Pharm (Weinheim). 2000 Sep;333(9):299-304. doi: 10.1002/1521-4184(20009)333:9<299::aid-ardp299>3.0.co;2-f. Arch Pharm (Weinheim). 2000. PMID: 11039186

2

Synthesis and antifungal properties of N-[(1,1'-biphenyl)-4-ylmethyl]-1H-imidazol-1-amine derivatives.

Setzu MG, Stefancich G, La Colla P, Castellano S. Setzu MG, et al. Among authors: castellano s. Farmaco. 2002 Dec;57(12):1015-8. doi: 10.1016/s0014-827x(02)01294-6. Farmaco. 2002. PMID: 12564477

3

Synthesis and antimicrobial properties of 3-aryl-1-(1,1'-biphenyl-4-yl)-2-(1H-imidazol-1-yl)propanes as 'carba-analogues' of the N-arylmethyl-N-[(1,1'-biphenyl)-4-ylmethyl])-1H-imidazol-1-amines, a new class of antifungal agents.

Castellano S, Stefancich G, Chillotti A, Poni G. Castellano S, et al. Farmaco. 2003 Aug;58(8):563-8. doi: 10.1016/S0014-827X(03)00094-6. Farmaco. 2003. PMID: 12875886

4

New structural analogues of Tubulozole induce apoptosis, [Ca2+]i modifications and cytoskeletal disorganization in glial (GL15) and neuronal-like (PC12) cell lines.

Castellano S, Mariggiò MA, Guarnieri S, Stefancich G, Pietrangelo T. Castellano S, et al. Arch Pharm (Weinheim). 2000 Nov;333(11):373-80. doi: 10.1002/1521-4184(200011)333:11<373::aid-ardp373>3.0.co;2-6. Arch Pharm (Weinheim). 2000. PMID: 11129979

5

Azole antifungal agents related to naftifine and butenafine.

Castellano S, La Colla P, Musiu C, Stefancich G. Castellano S, et al. Arch Pharm (Weinheim). 2000 Jun;333(6):162-6. Arch Pharm (Weinheim). 2000. PMID: 10909187

6

Synthesis of 11-aryl-5H-imidazo[2,1-c][1,4]benzodiazepines and their benzodiazepine and A1 adenosine binding activity.

Castellano S, Zorzin L, Florio C, Frausin F, Stefancich G. Castellano S, et al. Farmaco. 2001 Oct;56(10):771-8. doi: 10.1016/s0014-827x(01)01133-8. Farmaco. 2001. PMID: 11718270

7

5-aryl-imidazo[2,1-c][1,4]benzodiazepine derivatives as tricyclic constrained analogues of diazepam and Ro5-4864. Synthesis and binding properties at peripheral and central benzodiazepine receptors.

Rizzetto E, Castellano S, Florio C, Vadori M, Stefancich G. Rizzetto E, et al. Among authors: castellano s. Pharmazie. 2006 Jun;61(6):505-10. doi: 10.1002/chin.200639192. Pharmazie. 2006. PMID: 16826968

8

CYP19 (aromatase): exploring the scaffold flexibility for novel selective inhibitors.

Castellano S, Stefancich G, Ragno R, Schewe K, Santoriello M, Caroli A, Hartmann RW, Sbardella G. Castellano S, et al. Bioorg Med Chem. 2008 Sep 15;16(18):8349-58. doi: 10.1016/j.bmc.2008.08.046. Epub 2008 Aug 26. Bioorg Med Chem. 2008. PMID: 18782670

9

Synthesis and biological evaluation of 4-phenylquinazoline-2-carboxamides designed as a novel class of potent ligands of the translocator protein.

Castellano S, Taliani S, Milite C, Pugliesi I, Da Pozzo E, Rizzetto E, Bendinelli S, Costa B, Cosconati S, Greco G, Novellino E, Sbardella G, Stefancich G, Martini C, Da Settimo F. Castellano S, et al. J Med Chem. 2012 May 10;55(9):4506-10. doi: 10.1021/jm201703k. Epub 2012 Apr 25. J Med Chem. 2012. PMID: 22489952

10

Design and synthesis of novel [60]fullerene derivatives as potential HIV aspartic protease inhibitors.

Marcorin GL, Da Ros T, Castellano S, Stefancich G, Bonin I, Miertus S, Prato M. Marcorin GL, et al. Among authors: castellano s. Org Lett. 2000 Dec 14;2(25):3955-8. doi: 10.1021/ol000217y. Org Lett. 2000. PMID: 11112616

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