Similar articles for PMID: 31294975

Year	Number of Results
1999	1
2000	2
2001	2
2002	1
2003	1
2004	4
2005	5
2006	5
2007	5
2008	9
2009	9
2010	3
2011	3
2012	4
2013	4
2014	12
2015	8
2016	3
2017	7
2018	7
2019	13
2020	2
2021	5
2024	0

1

Discovery of Novel Naphthylphenylketone and Naphthylphenylamine Derivatives as Cell Division Cycle 25B (CDC25B) Phosphatase Inhibitors: Design, Synthesis, Inhibition Mechanism, and in Vitro Efficacy against Melanoma Cell Lines.

Cerchia C, Nasso R, Mori M, Villa S, Gelain A, Capasso A, Aliotta F, Simonetti M, Rullo R, Masullo M, De Vendittis E, Ruocco MR, Lavecchia A. Cerchia C, et al. J Med Chem. 2019 Aug 8;62(15):7089-7110. doi: 10.1021/acs.jmedchem.9b00632. Epub 2019 Jul 24. J Med Chem. 2019. PMID: 31294975

2

Inhibition mechanism of naphthylphenylamine derivatives acting on the CDC25B dual phosphatase and analysis of the molecular processes involved in the high cytotoxicity exerted by one selected derivative in melanoma cells.

Aliotta F, Nasso R, Rullo R, Arcucci A, Avagliano A, Simonetti M, Sanità G, Masullo M, Lavecchia A, Ruocco MR, Vendittis E. Aliotta F, et al. J Enzyme Inhib Med Chem. 2020 Dec;35(1):1866-1878. doi: 10.1080/14756366.2020.1819257. J Enzyme Inhib Med Chem. 2020. PMID: 32990107 Free PMC article.

3

Ligand-based chemoinformatic discovery of a novel small molecule inhibitor targeting CDC25 dual specificity phosphatases and displaying in vitro efficacy against melanoma cells.

Capasso A, Cerchia C, Di Giovanni C, Granato G, Albano F, Romano S, De Vendittis E, Ruocco MR, Lavecchia A. Capasso A, et al. Oncotarget. 2015 Nov 24;6(37):40202-22. doi: 10.18632/oncotarget.5473. Oncotarget. 2015. PMID: 26474275 Free PMC article.

4

2,4-Dihydroxychalcone derivatives as novel potent cell division cycle 25B phosphatase inhibitors and protein tyrosine phosphatase 1B inhibitors.

Xie C, Sun Y, Pan CY, Tang LM, Guan LP. Xie C, et al. Pharmazie. 2014 Apr;69(4):257-62. Pharmazie. 2014. PMID: 24791588

5

Discovery of potent and selective Cdc25 phosphatase inhibitors via rapid assembly and in situ screening of Quinonoid-focused libraries.

Tao Y, Hao X, Jing L, Sun L, Cherukupalli S, Liu S, Wu G, Xu S, Zhang X, Shi X, Song Y, Liu X, Zhan P. Tao Y, et al. Bioorg Chem. 2021 Oct;115:105254. doi: 10.1016/j.bioorg.2021.105254. Epub 2021 Aug 9. Bioorg Chem. 2021. PMID: 34426152

6

Cdc25B dual-specificity phosphatase inhibitors identified in a high-throughput screen of the NIH compound library.

Johnston PA, Foster CA, Tierno MB, Shun TY, Shinde SN, Paquette WD, Brummond KM, Wipf P, Lazo JS. Johnston PA, et al. Assay Drug Dev Technol. 2009 Jun;7(3):250-65. doi: 10.1089/adt.2008.186. Assay Drug Dev Technol. 2009. PMID: 19530895 Free PMC article.

7

Design, synthesis, and biological evaluation of novel naphthoquinone derivatives with CDC25 phosphatase inhibitory activity.

Brun MP, Braud E, Angotti D, Mondésert O, Quaranta M, Montes M, Miteva M, Gresh N, Ducommun B, Garbay C. Brun MP, et al. Bioorg Med Chem. 2005 Aug 15;13(16):4871-9. doi: 10.1016/j.bmc.2005.05.005. Bioorg Med Chem. 2005. PMID: 15921913

8

Synthesis and biological evaluation of 3-aminoisoquinolin-1(2H)-one based inhibitors of the dual-specificity phosphatase Cdc25B.

George Rosenker KM, Paquette WD, Johnston PA, Sharlow ER, Vogt A, Bakan A, Lazo JS, Wipf P. George Rosenker KM, et al. Bioorg Med Chem. 2015 Jun 15;23(12):2810-8. doi: 10.1016/j.bmc.2015.01.043. Epub 2015 Jan 31. Bioorg Med Chem. 2015. PMID: 25703307

9

Discovery of new inhibitors of Cdc25B dual specificity phosphatases by structure-based virtual screening.

Lavecchia A, Di Giovanni C, Pesapane A, Montuori N, Ragno P, Martucci NM, Masullo M, De Vendittis E, Novellino E. Lavecchia A, et al. J Med Chem. 2012 May 10;55(9):4142-58. doi: 10.1021/jm201624h. Epub 2012 May 1. J Med Chem. 2012. PMID: 22524450

10

Chalcones derivatives as potent Cell division cycle 25B phosphatase inhibitors.

Zhang J, Ji FJ, Gu Y, Zhang XY, Qiao SX. Zhang J, et al. Pharmacol Rep. 2014 Jun;66(3):515-9. doi: 10.1016/j.pharep.2013.08.016. Epub 2014 Mar 4. Pharmacol Rep. 2014. PMID: 24905533

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