Similar articles for PMID: 23792316

Year	Number of Results
2002	2
2003	2
2004	1
2005	3
2006	2
2007	7
2008	3
2009	8
2010	20
2011	17
2012	17
2013	36
2014	35
2015	27
2016	27
2017	26
2018	18
2019	18
2020	14
2021	5
2022	3
2024	0

1

Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring.

Guandalini L, Balliu M, Cellai C, Martino MV, Nebbioso A, Mercurio C, Carafa V, Bartolucci G, Dei S, Manetti D, Teodori E, Scapecchi S, Altucci L, Paoletti F, Romanelli MN. Guandalini L, et al. Eur J Med Chem. 2013 Aug;66:56-68. doi: 10.1016/j.ejmech.2013.05.017. Epub 2013 May 31. Eur J Med Chem. 2013. PMID: 23792316

2

Design, synthesis and preliminary bioactivity studies of 1,3,4-thiadiazole hydroxamic acid derivatives as novel histone deacetylase inhibitors.

Guan P, Sun F, Hou X, Wang F, Yi F, Xu W, Fang H. Guan P, et al. Bioorg Med Chem. 2012 Jun 15;20(12):3865-72. doi: 10.1016/j.bmc.2012.04.032. Epub 2012 Apr 21. Bioorg Med Chem. 2012. PMID: 22579621

3

Synthesis and antitumor activity of novel diaryl ether hydroxamic acids derivatives as potential HDAC inhibitors.

Zhu Y, Chen X, Wu Z, Zheng Y, Chen Y, Tang W, Lu T. Zhu Y, et al. Arch Pharm Res. 2012 Oct;35(10):1723-32. doi: 10.1007/s12272-012-1003-0. Epub 2012 Nov 9. Arch Pharm Res. 2012. PMID: 23139122

4

Design, synthesis and anticancer activity of piperazine hydroxamates and their histone deacetylase (HDAC) inhibitory activity.

Chetan B, Bunha M, Jagrat M, Sinha BN, Saiko P, Graser G, Szekeres T, Raman G, Rajendran P, Moorthy D, Basu A, Jayaprakash V. Chetan B, et al. Bioorg Med Chem Lett. 2010 Jul 1;20(13):3906-10. doi: 10.1016/j.bmcl.2010.05.020. Epub 2010 May 15. Bioorg Med Chem Lett. 2010. PMID: 20605448

5

Identification of a series of substituted 2-piperazinyl-5-pyrimidylhydroxamic acids as potent histone deacetylase inhibitors.

Angibaud P, Van Emelen K, Decrane L, van Brandt S, Ten Holte P, Pilatte I, Roux B, Poncelet V, Speybrouck D, Queguiner L, Gaurrand S, Mariën A, Floren W, Janssen L, Verdonck M, van Dun J, van Gompel J, Gilissen R, Mackie C, Du Jardin M, Peeters J, Noppe M, Van Hijfte L, Freyne E, Page M, Janicot M, Arts J. Angibaud P, et al. Bioorg Med Chem Lett. 2010 Jan 1;20(1):294-8. doi: 10.1016/j.bmcl.2009.10.118. Epub 2009 Oct 30. Bioorg Med Chem Lett. 2010. PMID: 19906529

6

Design and synthesis of dual-action inhibitors targeting histone deacetylases and 3-hydroxy-3-methylglutaryl coenzyme A reductase for cancer treatment.

Chen JB, Chern TR, Wei TT, Chen CC, Lin JH, Fang JM. Chen JB, et al. J Med Chem. 2013 May 9;56(9):3645-55. doi: 10.1021/jm400179b. Epub 2013 Apr 22. J Med Chem. 2013. PMID: 23570542

7

Design and synthesis of novel and highly-active pan-histone deacetylase (pan-HDAC) inhibitors.

Tashima T, Murata H, Kodama H. Tashima T, et al. Bioorg Med Chem. 2014 Jul 15;22(14):3720-31. doi: 10.1016/j.bmc.2014.05.001. Epub 2014 May 14. Bioorg Med Chem. 2014. PMID: 24864038

8

tert-Butylcarbamate-containing histone deacetylase inhibitors: apoptosis induction, cytodifferentiation, and antiproliferative activities in cancer cells.

Valente S, Trisciuoglio D, Tardugno M, Benedetti R, Labella D, Secci D, Mercurio C, Boggio R, Tomassi S, Di Maro S, Novellino E, Altucci L, Del Bufalo D, Mai A, Cosconati S. Valente S, et al. ChemMedChem. 2013 May;8(5):800-11. doi: 10.1002/cmdc.201300005. Epub 2013 Mar 25. ChemMedChem. 2013. PMID: 23526814

9

Improved antiproliferative activity of 1,3,4-thiadiazole-containing histone deacetylase (HDAC) inhibitors by introduction of the heteroaromatic surface recognition motif.

Guan P, Wang L, Hou X, Wan Y, Xu W, Tang W, Fang H. Guan P, et al. Bioorg Med Chem. 2014 Nov 1;22(21):5766-75. doi: 10.1016/j.bmc.2014.09.039. Epub 2014 Sep 28. Bioorg Med Chem. 2014. PMID: 25311567

10

Design, synthesis, and biological activity of NCC149 derivatives as histone deacetylase 8-selective inhibitors.

Suzuki T, Muto N, Bando M, Itoh Y, Masaki A, Ri M, Ota Y, Nakagawa H, Iida S, Shirahige K, Miyata N. Suzuki T, et al. ChemMedChem. 2014 Mar;9(3):657-64. doi: 10.1002/cmdc.201300414. Epub 2014 Jan 8. ChemMedChem. 2014. PMID: 24403121

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