Bernardi A - Search Results

1

Interfering with the sugar code: design and synthesis of oligosaccharide mimics.

Bernardi A, Cheshev P. Bernardi A, et al. Chemistry. 2008;14(25):7434-41. doi: 10.1002/chem.200800597. Chemistry. 2008. PMID: 18613175 Review.

2

Second generation mimics of ganglioside GM1 as artificial receptors for cholera toxin: replacement of the sialic acid moiety.

Bernardi A, Carrettoni L, Ciponte AG, Monti D, Sonnino S. Bernardi A, et al. Bioorg Med Chem Lett. 2000 Oct 2;10(19):2197-200. doi: 10.1016/s0960-894x(00)00428-5. Bioorg Med Chem Lett. 2000. PMID: 11012028

3

Simulation of carbohydrate-protein interactions: computer-aided design of a second generation GM1 mimic.

Bernardi A, Galgano M, Belvisi L, Colombo G. Bernardi A, et al. J Comput Aided Mol Des. 2001 Feb;15(2):117-28. doi: 10.1023/a:1008145830153. J Comput Aided Mol Des. 2001. PMID: 11272699

We recently reported that the pseudosaccharide 2 [Galbeta1-3GalNAcbeta1-4(NeuAcalpha2-3)DCCHD] is a high-affinity ligand for CT. and thus a functional mimic of GM1 (Bernardi, A., Checchia, A., Brocca, P., Sonnino, S. and Zuccotto, F., J. ...Soc. …

We recently reported that the pseudosaccharide 2 [Galbeta1-3GalNAcbeta1-4(NeuAcalpha2-3)DCCHD] is a high-affinity ligand for CT. and …

4

Second-generation mimics of ganglioside GM1 oligosaccharide: a three-dimensional view of their interactions with bacterial enterotoxins by NMR and computational methods.

Bernardi A, Potenza D, Capelli AM, García-Herrero A, Cañada FJ, Jiménez-Barbero J. Bernardi A, et al. Chemistry. 2002 Oct 18;8(20):4597-612. doi: 10.1002/1521-3765(20021018)8:20<4597::AID-CHEM4597>3.0.CO;2-U. Chemistry. 2002. PMID: 12362397

5

Mimicking gangliosides by design: mimics of GM1 headgroup.

Bernardi A, Arosio D, Sonnino S. Bernardi A, et al. Neurochem Res. 2002 Aug;27(7-8):539-45. doi: 10.1023/a:1020251428217. Neurochem Res. 2002. PMID: 12374188 Review.

6

Second-generation mimics of ganglioside GM1 oligosaccharide: a three-dimensional view of their interactions with bacterial enterotoxins by NMR and computational methods.

Bernardi A, Potenza D, Capelli AM, García-Herrero A, Cañada FJ, Jiménez-Barbero J. Bernardi A, et al. Chemistry. 2002 Oct 18;8(20):4598-612. Chemistry. 2002. PMID: 12561103

7

Mimics of ganglioside GM1 as cholera toxin ligands: replacement of the GalNAc residue.

Bernardi A, Arosio D, Manzoni L, Monti D, Posteri H, Potenza D, Mari S, Jiménez-Barbero J. Bernardi A, et al. Org Biomol Chem. 2003 Mar 7;1(5):785-92. doi: 10.1039/b210503a. Org Biomol Chem. 2003. PMID: 12929360

8

Ganglioside GM1 mimics: lipophilic substituents improve affinity for cholera toxin.

Arosio D, Baretti S, Cattaldo S, Potenza D, Bernardi A. Arosio D, et al. Among authors: bernardi a. Bioorg Med Chem Lett. 2003 Nov 3;13(21):3831-4. doi: 10.1016/j.bmcl.2003.07.007. Bioorg Med Chem Lett. 2003. PMID: 14552790

9

Synthesis and cholera toxin binding properties of multivalent GM1 mimics.

Arosio D, Vrasidas I, Valentini P, Liskamp RM, Pieters RJ, Bernardi A. Arosio D, et al. Among authors: bernardi a. Org Biomol Chem. 2004 Jul 21;2(14):2113-24. doi: 10.1039/b405344c. Epub 2004 Jun 30. Org Biomol Chem. 2004. PMID: 15254640

10

Intramolecular carbohydrate-aromatic interactions and intermolecular van der Waals interactions enhance the molecular recognition ability of GM1 glycomimetics for cholera toxin.

Bernardi A, Arosio D, Potenza D, Sánchez-Medina I, Mari S, Cañada FJ, Jiménez-Barbero J. Bernardi A, et al. Chemistry. 2004 Sep 20;10(18):4395. doi: 10.1002/chem.200400084. Chemistry. 2004. PMID: 15378617

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