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.
434 related articles for article (PubMed ID: 26890116)
21. Exploration of certain 1,3-oxazole- and 1,3-thiazole-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents. Anh DT; Hai PT; Huong LT; Park EJ; Jun HW; Kang JS; Kwon JH; Dung DTM; Anh VT; Hue VTM; Han SB; Nam NH Bioorg Chem; 2020 Aug; 101():103988. PubMed ID: 32534346 [TBL] [Abstract][Full Text] [Related]
22. Effect of C7-substitution of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines on the selectivity towards a subclass of histone deacetylases. Lee HY; Wang LT; Li YH; Pan SL; Chen YL; Teng CM; Liou JP Org Biomol Chem; 2014 Nov; 12(44):8966-76. PubMed ID: 25277250 [TBL] [Abstract][Full Text] [Related]
23. Design, synthesis and biological evaluation of indeno[1,2-d]thiazole derivatives as potent histone deacetylase inhibitors. Zhou M; Ning C; Liu R; He Y; Yu N Bioorg Med Chem Lett; 2013 Jun; 23(11):3200-3. PubMed ID: 23639537 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. 5-aryl-1,3,4-thiadiazole-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents: synthesis, bioevaluation and docking study. Huong TT; Dung do TM; Oanh DT; Lan TT; Dung PT; Loi VD; Kim KR; Han BW; Yun J; Kang JS; Kim Y; Han SB; Nam NH Med Chem; 2015; 11(3):296-304. PubMed ID: 25256241 [TBL] [Abstract][Full Text] [Related]
26. Synthesis and biological evaluation of 3-(4-substituted-phenyl)-N-hydroxy-2-propenamides, a new class of histone deacetylase inhibitors. Kim DK; Lee JY; Kim JS; Ryu JH; Choi JY; Lee JW; Im GJ; Kim TK; Seo JW; Park HJ; Yoo J; Park JH; Kim TY; Bang YJ J Med Chem; 2003 Dec; 46(26):5745-51. PubMed ID: 14667227 [TBL] [Abstract][Full Text] [Related]
27. Design, synthesis and preliminary bioactivity evaluations of substituted quinoline hydroxamic acid derivatives as novel histone deacetylase (HDAC) inhibitors. Wang L; Hou X; Fu H; Pan X; Xu W; Tang W; Fang H Bioorg Med Chem; 2015 Aug; 23(15):4364-4374. PubMed ID: 26149591 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. 1-Aroylindoline-hydroxamic acids as anticancer agents, inhibitors of HSP90 and HDAC. Ojha R; Huang HL; HuangFu WC; Wu YW; Nepali K; Lai MJ; Su CJ; Sung TY; Chen YL; Pan SL; Liou JP Eur J Med Chem; 2018 Apr; 150():667-677. PubMed ID: 29567459 [TBL] [Abstract][Full Text] [Related]
30. 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 Bioorg Med Chem Lett; 2010 Jan; 20(1):294-8. PubMed ID: 19906529 [TBL] [Abstract][Full Text] [Related]
31. (7-Diethylaminocoumarin-4-yl)methyl ester of suberoylanilide hydroxamic acid as a caged inhibitor for photocontrol of histone deacetylase activity. Ieda N; Yamada S; Kawaguchi M; Miyata N; Nakagawa H Bioorg Med Chem; 2016 Jun; 24(12):2789-93. PubMed ID: 27143132 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Design, synthesis and biological evaluation of tyrosine-based hydroxamic acid analogs as novel histone deacetylases (HDACs) inhibitors. Zhang Y; Feng J; Liu C; Fang H; Xu W Bioorg Med Chem; 2011 Aug; 19(15):4437-44. PubMed ID: 21733698 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Novel Hydroxamic Acids Incorporating 1-((1H-1,2,3-Triazol-4-yl)methyl)- 3-substituted-2-oxoindolines: Synthesis, Biological Evaluation and SAR Analysis. Dung DTM; Huan NV; Cam DM; Hieu DC; Hai PT; Huong LT; Kim J; Choi JE; Kang JS; Han SB; Nam NH Med Chem; 2018; 14(8):831-850. PubMed ID: 29807520 [TBL] [Abstract][Full Text] [Related]
36. New benzothiazole/thiazole-containing hydroxamic acids as potent histone deacetylase inhibitors and antitumor agents. Tung TT; Oanh DT; Dung PT; Hue VT; Park SH; Han BW; Kim Y; Hong JT; Han SB; Nam NH Med Chem; 2013 Dec; 9(8):1051-7. PubMed ID: 23521008 [TBL] [Abstract][Full Text] [Related]
37. Novel N-hydroxybenzamides incorporating 2-oxoindoline with unexpected potent histone deacetylase inhibitory effects and antitumor cytotoxicity. Huong TT; Dung DT; Huan NV; Cuong LV; Hai PT; Huong LT; Kim J; Kim YG; Han SB; Nam NH Bioorg Chem; 2017 Apr; 71():160-169. PubMed ID: 28196602 [TBL] [Abstract][Full Text] [Related]
38. Development of Coumarin-Based Hydroxamates as Histone Deacetylase Inhibitors with Antitumor Activities. Zhao N; Yang F; Han L; Qu Y; Ge D; Zhang H Molecules; 2020 Feb; 25(3):. PubMed ID: 32046013 [TBL] [Abstract][Full Text] [Related]
39. Development of tetrahydroisoquinoline-based hydroxamic acid derivatives: potent histone deacetylase inhibitors with marked in vitro and in vivo antitumor activities. Zhang Y; Feng J; Jia Y; Wang X; Zhang L; Liu C; Fang H; Xu W J Med Chem; 2011 Apr; 54(8):2823-38. PubMed ID: 21476600 [TBL] [Abstract][Full Text] [Related]
40. 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 Bioorg Med Chem; 2014 Nov; 22(21):5766-75. PubMed ID: 25311567 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]