Taddei M - Search Results

1

A pH-responsive crosslinker platform for antibody-drug conjugate (ADC) targeting delivery.

Migliorini F, Cini E, Dreassi E, Finetti F, Ievoli G, Macrì G, Petricci E, Rango E, Trabalzini L, Taddei M. Migliorini F, et al. Among authors: taddei m. Chem Commun (Camb). 2022 Sep 20;58(75):10532-10535. doi: 10.1039/d2cc03052g. Chem Commun (Camb). 2022. PMID: 36043993

2

Total synthesis, NMR solution structure, and binding model of the potent histone deacetylase inhibitor FR235222.

Rodriquez M, Terracciano S, Cini E, Settembrini G, Bruno I, Bifulco G, Taddei M, Gomez-Paloma L. Rodriquez M, et al. Among authors: taddei m. Angew Chem Int Ed Engl. 2006 Jan 9;45(3):423-7. doi: 10.1002/anie.200501995. Angew Chem Int Ed Engl. 2006. PMID: 16311994 No abstract available.

3

Synthesis of 2-amino-8-oxodecanoic acids (Aodas) present in natural hystone deacetylase inhibitors.

Rodriquez M, Bruno I, Cini E, Marchetti M, Taddei M, Gomez-Paloma L. Rodriquez M, et al. Among authors: taddei m. J Org Chem. 2006 Jan 6;71(1):103-7. doi: 10.1021/jo0518250. J Org Chem. 2006. PMID: 16388624

4

Microwaves make hydroformylation a rapid and easy process.

Petricci E, Mann A, Schoenfelder A, Rota A, Taddei M. Petricci E, et al. Among authors: taddei m. Org Lett. 2006 Aug 17;8(17):3725-7. doi: 10.1021/ol061312v. Org Lett. 2006. PMID: 16898802

5

Design and synthesis of cyclopeptide analogues of the potent histone deacetylase inhibitor FR235222.

Gomez-Paloma L, Bruno I, Cini E, Khochbin S, Rodriquez M, Taddei M, Terracciano S, Sadoul K. Gomez-Paloma L, et al. Among authors: taddei m. ChemMedChem. 2007 Oct;2(10):1511-9. doi: 10.1002/cmdc.200700095. ChemMedChem. 2007. PMID: 17694590

6

Microwave-assisted intramolecular Huisgen cycloaddition of azido alkynes derived from alpha-amino acids.

Balducci E, Bellucci L, Petricci E, Taddei M, Tafi A. Balducci E, et al. Among authors: taddei m. J Org Chem. 2009 Feb 6;74(3):1314-21. doi: 10.1021/jo802463r. J Org Chem. 2009. PMID: 19138079

7

Microwave-assisted carbonylation and cyclocarbonylation of aryl iodides under ligand free heterogeneous catalysis.

Salvadori J, Balducci E, Zaza S, Petricci E, Taddei M. Salvadori J, et al. Among authors: taddei m. J Org Chem. 2010 Mar 19;75(6):1841-7. doi: 10.1021/jo9021315. J Org Chem. 2010. PMID: 20184297

8

Oxime amides as a novel zinc binding group in histone deacetylase inhibitors: synthesis, biological activity, and computational evaluation.

Botta CB, Cabri W, Cini E, De Cesare L, Fattorusso C, Giannini G, Persico M, Petrella A, Rondinelli F, Rodriquez M, Russo A, Taddei M. Botta CB, et al. Among authors: taddei m. J Med Chem. 2011 Apr 14;54(7):2165-82. doi: 10.1021/jm101373a. Epub 2011 Mar 18. J Med Chem. 2011. PMID: 21417297

9

Downregulation of hypoxia-related responses by novel antitumor histone deacetylase inhibitors in MDAMB231 breast cancer cells.

Naldini A, Filippi I, Cini E, Rodriquez M, Carraro F, Taddei M. Naldini A, et al. Among authors: taddei m. Anticancer Agents Med Chem. 2012 May;12(4):407-13. doi: 10.2174/187152012800228706. Anticancer Agents Med Chem. 2012. PMID: 22043993

10

Lactam based 7-amino suberoylamide hydroxamic acids as potent HDAC inhibitors.

Taddei M, Cini E, Giannotti L, Giannini G, Battistuzzi G, Vignola D, Vesci L, Cabri W. Taddei M, et al. Bioorg Med Chem Lett. 2014 Jan 1;24(1):61-4. doi: 10.1016/j.bmcl.2013.11.072. Epub 2013 Dec 4. Bioorg Med Chem Lett. 2014. PMID: 24345446

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