La Motta C - Search Results

1

Nature-Inspired O-Benzyl Oxime-Based Derivatives as New Dual-Acting Agents Targeting Aldose Reductase and Oxidative Stress.

Ciccone L, Petrarolo G, Barsuglia F, Fruchart-Gaillard C, Cassar Lajeunesse E, Adewumi AT, Soliman MES, La Motta C, Orlandini E, Nencetti S. Ciccone L, et al. Among authors: la motta c. Biomolecules. 2022 Mar 14;12(3):448. doi: 10.3390/biom12030448. Biomolecules. 2022. PMID: 35327641 Free PMC article.

2

Acid derivatives of benzisothiazole-1,1-dioxide as inhibitors of rat lens aldose reductase.

Da Settimo A, Primofiore G, La Motta C, Da Settimo F, Simorini F, Boldrini E, Bianchini P. Da Settimo A, et al. Among authors: la motta c. Farmaco. 1996 Apr;51(4):261-7. Farmaco. 1996. PMID: 8645413

3

[1,2,4]Triazino[4,3-a]benzimidazole acetic acid derivatives: a new class of selective aldose reductase inhibitors.

Da Settimo F, Primofiore G, Da Settimo A, La Motta C, Taliani S, Simorini F, Novellino E, Greco G, Lavecchia A, Boldrini E. Da Settimo F, et al. Among authors: la motta c. J Med Chem. 2001 Dec 6;44(25):4359-69. doi: 10.1021/jm0109210. J Med Chem. 2001. PMID: 11728182

4

Naphtho[1,2-d]isothiazole acetic acid derivatives as a novel class of selective aldose reductase inhibitors.

Da Settimo F, Primofiore G, La Motta C, Sartini S, Taliani S, Simorini F, Marini AM, Lavecchia A, Novellino E, Boldrini E. Da Settimo F, et al. Among authors: la motta c. J Med Chem. 2005 Nov 3;48(22):6897-907. doi: 10.1021/jm050382p. J Med Chem. 2005. PMID: 16250648

5

Pyrido[1,2-a]pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity.

La Motta C, Sartini S, Mugnaini L, Simorini F, Taliani S, Salerno S, Marini AM, Da Settimo F, Lavecchia A, Novellino E, Cantore M, Failli P, Ciuffi M. La Motta C, et al. J Med Chem. 2007 Oct 4;50(20):4917-27. doi: 10.1021/jm070398a. Epub 2007 Sep 11. J Med Chem. 2007. PMID: 17845019

6

Tricyclic sulfonamides incorporating benzothiopyrano[4,3-c]pyrazole and pyridothiopyrano[4,3-c]pyrazole effectively inhibit α- and β-carbonic anhydrase: X-ray crystallography and solution investigations on 15 isoforms.

Marini AM, Maresca A, Aggarwal M, Orlandini E, Nencetti S, Da Settimo F, Salerno S, Simorini F, La Motta C, Taliani S, Nuti E, Scozzafava A, McKenna R, Rossello A, Supuran CT. Marini AM, et al. Among authors: la motta c. J Med Chem. 2012 Nov 26;55(22):9619-29. doi: 10.1021/jm300878g. Epub 2012 Nov 8. J Med Chem. 2012. PMID: 23067387

7

A new approach to control the enigmatic activity of aldose reductase.

Del-Corso A, Balestri F, Di Bugno E, Moschini R, Cappiello M, Sartini S, La-Motta C, Da-Settimo F, Mura U. Del-Corso A, et al. Among authors: la motta c. PLoS One. 2013 Sep 3;8(9):e74076. doi: 10.1371/journal.pone.0074076. eCollection 2013. PLoS One. 2013. PMID: 24019949 Free PMC article.

8

N-(Aroyl)-N-(arylmethyloxy)-α-alanines: Selective inhibitors of aldose reductase.

Nencetti S, La Motta C, Rossello A, Sartini S, Nuti E, Ciccone L, Orlandini E. Nencetti S, et al. Among authors: la motta c. Bioorg Med Chem. 2017 Jun 15;25(12):3068-3076. doi: 10.1016/j.bmc.2017.03.056. Epub 2017 Mar 28. Bioorg Med Chem. 2017. PMID: 28392277

9

Quinazolinone-based rhodanine-3-acetic acids as potent aldose reductase inhibitors: Synthesis, functional evaluation and molecular modeling study.

El-Sayed S, Metwally K, El-Shanawani AA, Abdel-Aziz LM, El-Rashedy AA, Soliman MES, Quattrini L, Coviello V, la Motta C. El-Sayed S, et al. Among authors: la motta c. Bioorg Med Chem Lett. 2017 Oct 15;27(20):4760-4764. doi: 10.1016/j.bmcl.2017.08.050. Epub 2017 Aug 24. Bioorg Med Chem Lett. 2017. PMID: 28935265

10

Acid Derivatives of Pyrazolo[1,5-a]pyrimidine as Aldose Reductase Differential Inhibitors.

Balestri F, Quattrini L, Coviello V, Sartini S, Da Settimo F, Cappiello M, Moschini R, Del Corso A, Mura U, La Motta C. Balestri F, et al. Among authors: la motta c. Cell Chem Biol. 2018 Nov 15;25(11):1414-1418.e3. doi: 10.1016/j.chembiol.2018.07.008. Epub 2018 Aug 16. Cell Chem Biol. 2018. PMID: 30122369 Free article.

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