These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
944 related articles for article (PubMed ID: 24864038)
1. Design and synthesis of novel and highly-active pan-histone deacetylase (pan-HDAC) inhibitors. Tashima T; Murata H; Kodama H Bioorg Med Chem; 2014 Jul; 22(14):3720-31. PubMed ID: 24864038 [TBL] [Abstract][Full Text] [Related]
2. The structural requirements of histone deacetylase inhibitors: C4-modified SAHA analogs display dual HDAC6/HDAC8 selectivity. Negmeldin AT; Knoff JR; Pflum MKH Eur J Med Chem; 2018 Jan; 143():1790-1806. PubMed ID: 29150330 [TBL] [Abstract][Full Text] [Related]
3. Quinazoline-Based Hydroxamic Acids: Design, Synthesis, and Evaluation of Histone Deacetylase Inhibitory Effects and Cytotoxicity. Hieu DT; Anh DT; Hai PT; Huong LT; Park EJ; Choi JE; Kang JS; Dung PTP; Han SB; Nam NH Chem Biodivers; 2018 Jun; 15(6):e1800027. PubMed ID: 29667768 [TBL] [Abstract][Full Text] [Related]
4. Lactam based 7-amino suberoylamide hydroxamic acids as potent HDAC inhibitors. Taddei M; Cini E; Giannotti L; Giannini G; Battistuzzi G; Vignola D; Vesci L; Cabri W Bioorg Med Chem Lett; 2014 Jan; 24(1):61-4. PubMed ID: 24345446 [TBL] [Abstract][Full Text] [Related]
5. 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 Bioorg Med Chem; 2012 Jun; 20(12):3865-72. PubMed ID: 22579621 [TBL] [Abstract][Full Text] [Related]
6. 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 ChemMedChem; 2014 Mar; 9(3):657-64. PubMed ID: 24403121 [TBL] [Abstract][Full Text] [Related]
7. Amide-based derivatives of β-alanine hydroxamic acid as histone deacetylase inhibitors: attenuation of potency through resonance effects. Liao V; Liu T; Codd R Bioorg Med Chem Lett; 2012 Oct; 22(19):6200-4. PubMed ID: 22932316 [TBL] [Abstract][Full Text] [Related]
8. Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors. Pabba C; Gregg BT; Kitchen DB; Chen ZJ; Judkins A Bioorg Med Chem Lett; 2011 Jan; 21(1):324-8. PubMed ID: 21109435 [TBL] [Abstract][Full Text] [Related]
9. Synthesis and applications of benzohydroxamic acid-based histone deacetylase inhibitors. De Vreese R; D'hooghe M Eur J Med Chem; 2017 Jul; 135():174-195. PubMed ID: 28453994 [TBL] [Abstract][Full Text] [Related]
10. 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 Bioorg Med Chem Lett; 2010 Jul; 20(13):3906-10. PubMed ID: 20605448 [TBL] [Abstract][Full Text] [Related]
11. An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors. Shahidul Islam M; Nurul Islam M; Ashraful Hoque M; Nishino N; Kato T; Kim HJ; Ito A; Yoshida M Bioorg Chem; 2015 Apr; 59():145-50. PubMed ID: 25797804 [TBL] [Abstract][Full Text] [Related]
12. Structural Requirements of Histone Deacetylase Inhibitors: SAHA Analogs Modified on the Hydroxamic Acid. Bieliauskas AV; Weerasinghe SV; Negmeldin AT; Pflum MK Arch Pharm (Weinheim); 2016 May; 349(5):373-82. PubMed ID: 27062198 [TBL] [Abstract][Full Text] [Related]
13. Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors. Huang WJ; Chen CC; Chao SW; Yu CC; Yang CY; Guh JH; Lin YC; Kuo CI; Yang P; Chang CI Eur J Med Chem; 2011 Sep; 46(9):4042-9. PubMed ID: 21712146 [TBL] [Abstract][Full Text] [Related]
14. Synthesis of N-hydroxycinnamides capped with a naturally occurring moiety as inhibitors of histone deacetylase. Huang WJ; Chen CC; Chao SW; Lee SS; Hsu FL; Lu YL; Hung MF; Chang CI ChemMedChem; 2010 Apr; 5(4):598-607. PubMed ID: 20209563 [TBL] [Abstract][Full Text] [Related]
15. 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 Arch Pharm Res; 2012 Oct; 35(10):1723-32. PubMed ID: 23139122 [TBL] [Abstract][Full Text] [Related]
16. Design, synthesis and anticancer evaluation of acridine hydroxamic acid derivatives as dual Topo and HDAC inhibitors. Chen J; Li D; Li W; Yin J; Zhang Y; Yuan Z; Gao C; Liu F; Jiang Y Bioorg Med Chem; 2018 Aug; 26(14):3958-3966. PubMed ID: 29954683 [TBL] [Abstract][Full Text] [Related]
17. Syntheses and Biological Evaluation of Novel Hydroxamic Acid Derivatives Containing Purine Moiety as Histone Deacetylase Inhibitors. Xu Z; Yang Y; Mai X; Liu B; Xiong Y; Feng L; Liao Y; Zhang Y; Wang H; Ouyang L; Liu S Chem Pharm Bull (Tokyo); 2018; 66(4):439-451. PubMed ID: 29607910 [TBL] [Abstract][Full Text] [Related]
18. Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors. Liu R; Wang J; Tang W; Fang H Bioorg Med Chem; 2016 Apr; 24(7):1446-54. PubMed ID: 26907204 [TBL] [Abstract][Full Text] [Related]
19. Quinazolin-4(3H)-one-Based Hydroxamic Acids: Design, Synthesis and Evaluation of Histone Deacetylase Inhibitory Effects and Cytotoxicity. Hieu DT; Anh DT; Hai PT; Thuan NT; Huong LT; Park EJ; Young Ji A; Soon Kang J; Phuong Dung PT; Han SB; Nam NH Chem Biodivers; 2019 Apr; 16(4):e1800502. PubMed ID: 30653817 [TBL] [Abstract][Full Text] [Related]
20. Synthesis and Biological Investigation of Oxazole Hydroxamates as Highly Selective Histone Deacetylase 6 (HDAC6) Inhibitors. Senger J; Melesina J; Marek M; Romier C; Oehme I; Witt O; Sippl W; Jung M J Med Chem; 2016 Feb; 59(4):1545-55. PubMed ID: 26653328 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]