Iraci N - Search Results

1

A Comprehensive Structural Overview of p38α MAPK in Complex with Type I Inhibitors.

Astolfi A, Iraci N, Manfroni G, Barreca ML, Cecchetti V. Astolfi A, et al. Among authors: iraci n. ChemMedChem. 2015 Jun;10(6):957-69. doi: 10.1002/cmdc.201500030. Epub 2015 Apr 9. ChemMedChem. 2015. PMID: 26012502 Review.

2

Amphiphilic Cyclodextrin Nanoparticles as Delivery System for Idebenone: A Preformulation Study.

De Gaetano F, Scala A, Celesti C, Lambertsen Larsen K, Genovese F, Bongiorno C, Leggio L, Iraci N, Iraci N, Mazzaglia A, Ventura CA. De Gaetano F, et al. Among authors: iraci n. Molecules. 2023 Mar 28;28(7):3023. doi: 10.3390/molecules28073023. Molecules. 2023. PMID: 37049785 Free PMC article.

3

Bicalutamide Anticancer Activity Enhancement by Formulation of Soluble Inclusion Complexes with Cyclodextrins.

De Gaetano F, Cristiano MC, Paolino D, Celesti C, Iannazzo D, Pistarà V, Iraci N, Ventura CA. De Gaetano F, et al. Among authors: iraci n. Biomolecules. 2022 Nov 19;12(11):1716. doi: 10.3390/biom12111716. Biomolecules. 2022. PMID: 36421730 Free PMC article.

4

Synergistic Combination of Citrus Flavanones as Strong Antioxidant and COX-Inhibitor Agent.

Smeriglio A, Iraci N, Denaro M, Mandalari G, Giofrè SV, Trombetta D. Smeriglio A, et al. Among authors: iraci n. Antioxidants (Basel). 2023 Apr 21;12(4):972. doi: 10.3390/antiox12040972. Antioxidants (Basel). 2023. PMID: 37107347 Free PMC article.

5

Binding mode prediction of strand transfer HIV-1 integrase inhibitors using Tn5 transposase as a plausible surrogate model for HIV-1 integrase.

Barreca ML, De Luca L, Iraci N, Chimirri A. Barreca ML, et al. Among authors: iraci n. J Med Chem. 2006 Jun 29;49(13):3994-7. doi: 10.1021/jm060323r. J Med Chem. 2006. PMID: 16789757

6

Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors.

Barreca ML, De Luca L, Iraci N, Rao A, Ferro S, Maga G, Chimirri A. Barreca ML, et al. Among authors: iraci n. J Chem Inf Model. 2007 Mar-Apr;47(2):557-62. doi: 10.1021/ci600320q. Epub 2007 Feb 3. J Chem Inf Model. 2007. PMID: 17274611

7

Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains.

Barreca ML, Rao A, De Luca L, Iraci N, Monforte AM, Maga G, De Clercq E, Pannecouque C, Balzarini J, Chimirri A. Barreca ML, et al. Among authors: iraci n. Bioorg Med Chem Lett. 2007 Apr 1;17(7):1956-60. doi: 10.1016/j.bmcl.2007.01.025. Epub 2007 Jan 19. Bioorg Med Chem Lett. 2007. PMID: 17276064

8

Tn5 transposase as a useful platform to simulate HIV-1 integrase inhibitor binding mode.

Barreca ML, Ortuso F, Iraci N, De Luca L, Alcaro S, Chimirri A. Barreca ML, et al. Among authors: iraci n. Biochem Biophys Res Commun. 2007 Nov 23;363(3):554-60. doi: 10.1016/j.bbrc.2007.08.199. Epub 2007 Sep 14. Biochem Biophys Res Commun. 2007. PMID: 17889829

9

A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole series.

De Luca L, Barreca ML, Ferro S, Iraci N, Michiels M, Christ F, Debyser Z, Witvrouw M, Chimirri A. De Luca L, et al. Among authors: iraci n. Bioorg Med Chem Lett. 2008 May 1;18(9):2891-5. doi: 10.1016/j.bmcl.2008.03.089. Epub 2008 Apr 8. Bioorg Med Chem Lett. 2008. PMID: 18417342

10

Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors.

Monforte AM, Rao A, Logoteta P, Ferro S, De Luca L, Barreca ML, Iraci N, Maga G, De Clercq E, Pannecouque C, Chimirri A. Monforte AM, et al. Among authors: iraci n. Bioorg Med Chem. 2008 Aug 1;16(15):7429-35. doi: 10.1016/j.bmc.2008.06.012. Epub 2008 Jun 13. Bioorg Med Chem. 2008. PMID: 18585918

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