Manetti F - Search Results

1

HIV-reverse transcriptase inhibition: inclusion of ligand-induced fit by cross-docking studies.

Ragno R, Frasca S, Manetti F, Brizzi A, Massa S. Ragno R, et al. Among authors: manetti f. J Med Chem. 2005 Jan 13;48(1):200-12. doi: 10.1021/jm0493921. J Med Chem. 2005. PMID: 15634014

2

Diltiazem-like calcium entry blockers: a hypothesis of the receptor-binding site based on a comparative molecular field analysis model.

Corelli F, Manetti F, Tafi A, Campiani G, Nacci V, Botta M. Corelli F, et al. Among authors: manetti f. J Med Chem. 1997 Jan 3;40(1):125-31. doi: 10.1021/jm9605647. J Med Chem. 1997. PMID: 9016337

3

Synthesis and binding mode of heterocyclic analogues of suramin inhibiting the human basic fibroblast growth factor.

Manetti F, Cappello V, Botta M, Corelli F, Mongelli N, Biasoli G, Borgia AL, Ciomei M. Manetti F, et al. Bioorg Med Chem. 1998 Jul;6(7):947-58. doi: 10.1016/s0968-0896(98)00052-2. Bioorg Med Chem. 1998. PMID: 9730230

4

Research on anti-HIV-1 agents. Investigation on the CD4-Suradista binding mode through docking experiments.

Manetti F, Corelli F, Mongelli N, Borgia AL, Botta M. Manetti F, et al. J Comput Aided Mol Des. 2000 May;14(4):355-68. doi: 10.1023/a:1008154931914. J Comput Aided Mol Des. 2000. PMID: 10815772

5

Building a pharmacophore model for a novel class of antitubercular compounds.

Manetti F, Corelli F, Biava M, Fioravanti R, Porretta GC, Botta M. Manetti F, et al. Farmaco. 2000 Jun-Jul;55(6-7):484-91. doi: 10.1016/s0014-827x(00)00072-0. Farmaco. 2000. PMID: 11204750

6

Synthesis, biological evaluation, and pharmacophore generation of new pyridazinone derivatives with affinity toward alpha(1)- and alpha(2)-adrenoceptors.

Barbaro R, Betti L, Botta M, Corelli F, Giannaccini G, Maccari L, Manetti F, Strappaghetti G, Corsano S. Barbaro R, et al. Among authors: manetti f. J Med Chem. 2001 Jun 21;44(13):2118-32. doi: 10.1021/jm010821u. J Med Chem. 2001. PMID: 11405649

7

Synthesis, biological evaluation, and pharmacophore generation of uracil, 4(3H)-pyrimidinone, and uridine derivatives as potent and selective inhibitors of parainfluenza 1 (Sendai) virus.

Saladino R, Crestini C, Palamara AT, Danti MC, Manetti F, Corelli F, Garaci E, Botta M. Saladino R, et al. Among authors: manetti f. J Med Chem. 2001 Dec 20;44(26):4554-62. doi: 10.1021/jm010938i. J Med Chem. 2001. PMID: 11741474

8

Synthesis and biological activity of new 1,4-benzodioxan-arylpiperazine derivatives. Further validation of a pharmacophore model for alpha(1)-adrenoceptor antagonists.

Barbaro R, Betti L, Botta M, Corelli F, Giannaccini G, Maccari L, Manetti F, Strappaghetti G, Corsano S. Barbaro R, et al. Among authors: manetti f. Bioorg Med Chem. 2002 Feb;10(2):361-9. doi: 10.1016/s0968-0896(01)00286-3. Bioorg Med Chem. 2002. PMID: 11741785

9

Arylpiperazines with affinity toward alpha(1)-adrenergic receptors.

Manetti F, Corelli F, Strappaghetti G, Botta M. Manetti F, et al. Curr Med Chem. 2002 Jul;9(13):1303-21. doi: 10.2174/0929867023369961. Curr Med Chem. 2002. PMID: 12052168 Review.

10

Antifungal agents. 10. New derivatives of 1-[(aryl)[4-aryl-1H-pyrrol-3-yl]methyl]-1H-imidazole, synthesis, anti-candida activity, and quantitative structure-analysis relationship studies.

Tafi A, Costi R, Botta M, Di Santo R, Corelli F, Massa S, Ciacci A, Manetti F, Artico M. Tafi A, et al. Among authors: manetti f. J Med Chem. 2002 Jun 20;45(13):2720-32. doi: 10.1021/jm011087h. J Med Chem. 2002. PMID: 12061875

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