Nurisso A - Search Results

1

Biphenyl-4-yl-acrylohydroxamic acids: Identification of a novel indolyl-substituted HDAC inhibitor with antitumor activity.

Cincinelli R, Zwick V, Musso L, Zuco V, De Cesare M, Zunino F, Simoes-Pires C, Nurisso A, Giannini G, Cuendet M, Dallavalle S. Cincinelli R, et al. Among authors: nurisso a. Eur J Med Chem. 2016 Apr 13;112:99-105. doi: 10.1016/j.ejmech.2016.02.001. Epub 2016 Feb 3. Eur J Med Chem. 2016. PMID: 26890116 Free article.

2

How to increase the safety and efficacy of compounds against neurodegeneration? A multifunctional approach.

Nurisso A, Simoes-Pires C, Martel S, Cressend D, Guillot A, Carrupt PA. Nurisso A, et al. Chimia (Aarau). 2012;66(5):286-90. doi: 10.2533/chimia.2012.286. Chimia (Aarau). 2012. PMID: 22867537 Free article. Review.

3

HDAC6 as a target for neurodegenerative diseases: what makes it different from the other HDACs?

Simões-Pires C, Zwick V, Nurisso A, Schenker E, Carrupt PA, Cuendet M. Simões-Pires C, et al. Among authors: nurisso a. Mol Neurodegener. 2013 Jan 29;8:7. doi: 10.1186/1750-1326-8-7. Mol Neurodegener. 2013. PMID: 23356410 Free PMC article. Review.

4

Non-specific SIRT inhibition as a mechanism for the cytotoxicity of ginkgolic acids and urushiols.

Ryckewaert L, Sacconnay L, Carrupt PA, Nurisso A, Simões-Pires C. Ryckewaert L, et al. Among authors: nurisso a. Toxicol Lett. 2014 Sep 2;229(2):374-80. doi: 10.1016/j.toxlet.2014.07.002. Epub 2014 Jul 3. Toxicol Lett. 2014. PMID: 24998427

5

Aurones as histone deacetylase inhibitors: identification of key features.

Zwick V, Chatzivasileiou AO, Deschamps N, Roussaki M, Simões-Pires CA, Nurisso A, Denis I, Blanquart C, Martinet N, Carrupt PA, Detsi A, Cuendet M. Zwick V, et al. Among authors: nurisso a. Bioorg Med Chem Lett. 2014 Dec 1;24(23):5497-501. doi: 10.1016/j.bmcl.2014.10.019. Epub 2014 Oct 13. Bioorg Med Chem Lett. 2014. PMID: 25455492

6

Alkaloids from psychotria target sirtuins: in silico and in vitro interaction studies.

Sacconnay L, Ryckewaert L, Dos Santos Passos C, Guerra MC, Kato L, Alves de Oliveira CM, Henriques A, Carrupt PA, Simões-Pires C, Nurisso A. Sacconnay L, et al. Among authors: nurisso a. Planta Med. 2015 Apr;81(6):517-24. doi: 10.1055/s-0034-1383261. Epub 2014 Dec 3. Planta Med. 2015. PMID: 25469857

7

How the flexibility of human histone deacetylases influences ligand binding: an overview.

Deschamps N, Simões-Pires CA, Carrupt PA, Nurisso A. Deschamps N, et al. Among authors: nurisso a. Drug Discov Today. 2015 Jun;20(6):736-42. doi: 10.1016/j.drudis.2015.01.004. Epub 2015 Jan 15. Drug Discov Today. 2015. PMID: 25597521 Review.

8

IPP51, a chalcone acting as a microtubule inhibitor with in vivo antitumor activity against bladder carcinoma.

Martel-Frachet V, Keramidas M, Nurisso A, DeBonis S, Rome C, Coll JL, Boumendjel A, Skoufias DA, Ronot X. Martel-Frachet V, et al. Among authors: nurisso a. Oncotarget. 2015 Jun 10;6(16):14669-86. doi: 10.18632/oncotarget.4144. Oncotarget. 2015. PMID: 26036640 Free PMC article.

9

Structure-Based Design and Optimization of Multitarget-Directed 2H-Chromen-2-one Derivatives as Potent Inhibitors of Monoamine Oxidase B and Cholinesterases.

Farina R, Pisani L, Catto M, Nicolotti O, Gadaleta D, Denora N, Soto-Otero R, Mendez-Alvarez E, Passos CS, Muncipinto G, Altomare CD, Nurisso A, Carrupt PA, Carotti A. Farina R, et al. Among authors: nurisso a. J Med Chem. 2015 Jul 23;58(14):5561-78. doi: 10.1021/acs.jmedchem.5b00599. Epub 2015 Jul 9. J Med Chem. 2015. PMID: 26107513

10

Investigation on the ZBG-functionality of phenyl-4-yl-acrylohydroxamic acid derivatives as histone deacetylase inhibitors.

Musso L, Cincinelli R, Zuco V, Zunino F, Nurisso A, Cuendet M, Giannini G, Vesci L, Pisano C, Dallavalle S. Musso L, et al. Among authors: nurisso a. Bioorg Med Chem Lett. 2015 Oct 15;25(20):4457-60. doi: 10.1016/j.bmcl.2015.09.006. Epub 2015 Sep 5. Bioorg Med Chem Lett. 2015. PMID: 26376355 Free article.

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