Moro S - Search Results

1

2-aryl-8-chloro-1,2,4-triazolo[1,5-a]quinoxalin-4-amines as highly potent A1 and A3 adenosine receptor antagonists.

Catarzi D, Colotta V, Varano F, Calabri FR, Lenzi O, Filacchioni G, Trincavelli L, Martini C, Tralli A, Montopoli C, Moro S. Catarzi D, et al. Among authors: moro s. Bioorg Med Chem. 2005 Feb 1;13(3):705-15. doi: 10.1016/j.bmc.2004.10.050. Bioorg Med Chem. 2005. PMID: 15653338

2

Flavonoid derivatives as adenosine receptor antagonists: a comparison of the hypothetical receptor binding site based on a comparative molecular field analysis model.

Moro S, van Rhee AM, Sanders LH, Jacobson KA. Moro S, et al. J Med Chem. 1998 Jan 1;41(1):46-52. doi: 10.1021/jm970446z. J Med Chem. 1998. PMID: 9438021 Free PMC article.

3

Derivatives of the triazoloquinazoline adenosine antagonist (CGS 15943) having high potency at the human A2B and A3 receptor subtypes.

Kim YC, de Zwart M, Chang L, Moro S, von Frijtag Drabbe Künzel JK, Melman N, IJzerman AP, Jacobson KA. Kim YC, et al. Among authors: moro s. J Med Chem. 1998 Jul 16;41(15):2835-45. doi: 10.1021/jm980094b. J Med Chem. 1998. PMID: 9667972 Free PMC article.

4

Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.

Li AH, Moro S, Melman N, Ji XD, Jacobson KA. Li AH, et al. Among authors: moro s. J Med Chem. 1998 Aug 13;41(17):3186-201. doi: 10.1021/jm980093j. J Med Chem. 1998. PMID: 9703464 Free PMC article.

5

Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2, 4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.

Li AH, Moro S, Forsyth N, Melman N, Ji XD, Jacobson KA. Li AH, et al. Among authors: moro s. J Med Chem. 1999 Feb 25;42(4):706-21. doi: 10.1021/jm980550w. J Med Chem. 1999. PMID: 10052977 Free PMC article.

6

Chiral resolution and stereospecificity of 6-phenyl-4-phenylethynyl- 1,4-dihydropyridines as selective A(3) adenosine receptor antagonists.

Jiang J, Li AH, Jang SY, Chang L, Melman N, Moro S, Ji X, Lobkovsky EB, Clardy JC, Jacobson KA. Jiang J, et al. Among authors: moro s. J Med Chem. 1999 Aug 12;42(16):3055-65. doi: 10.1021/jm980688e. J Med Chem. 1999. PMID: 10447949 Free PMC article.

7

6-Aminoquinolones as new potential anti-HIV agents.

Cecchetti V, Parolin C, Moro S, Pecere T, Filipponi E, Calistri A, Tabarrini O, Gatto B, Palumbo M, Fravolini A, Palu' G. Cecchetti V, et al. Among authors: moro s. J Med Chem. 2000 Oct 5;43(20):3799-802. doi: 10.1021/jm9903390. J Med Chem. 2000. PMID: 11020296

8

Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists: influence of the chain at the N(8) pyrazole nitrogen.

Baraldi PG, Cacciari B, Romagnoli R, Spalluto G, Moro S, Klotz KN, Leung E, Varani K, Gessi S, Merighi S, Borea PA. Baraldi PG, et al. Among authors: moro s. J Med Chem. 2000 Dec 14;43(25):4768-80. doi: 10.1021/jm001047y. J Med Chem. 2000. PMID: 11123985

9

Fluorosulfonyl- and bis-(beta-chloroethyl)amino-phenylamino functionalized pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: irreversible antagonists at the human A3 adenosine receptor and molecular modeling studies.

Baraldi PG, Cacciari B, Moro S, Romagnoli R, Ji Xd, Jacobson KA, Gessi S, Borea PA, Spalluto G. Baraldi PG, et al. Among authors: moro s. J Med Chem. 2001 Aug 16;44(17):2735-42. doi: 10.1021/jm010818a. J Med Chem. 2001. PMID: 11495585

10

Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists.

Baraldi PG, Cacciari B, Moro S, Spalluto G, Pastorin G, Da Ros T, Klotz KN, Varani K, Gessi S, Borea PA. Baraldi PG, et al. Among authors: moro s. J Med Chem. 2002 Feb 14;45(4):770-80. doi: 10.1021/jm0109614. J Med Chem. 2002. PMID: 11831890

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