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.
490 related articles for article (PubMed ID: 26732459)
21. 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]
22. Design, synthesis and biological evaluation of novel indazole-based derivatives as potent HDAC inhibitors via fragment-based virtual screening. Liu J; Zhou J; He F; Gao L; Wen Y; Gao L; Wang P; Kang D; Hu L Eur J Med Chem; 2020 Apr; 192():112189. PubMed ID: 32151834 [TBL] [Abstract][Full Text] [Related]
23. Design, Synthesis and Biological Evaluation of Novel N-hydroxyheptanamides Incorporating 6-hydroxy-2-methylquinazolin-4(3H)-ones as Histone Deacetylase Inhibitors and Cytotoxic Agents. Minh NV; Thanh NT; Lien HT; Anh DTP; Cuong HD; Nam NH; Hai PT; Minh-Ngoc L; Le-Thi-Thu H; Chinh LV; Vu TK Anticancer Agents Med Chem; 2019; 19(12):1543-1557. PubMed ID: 31267876 [TBL] [Abstract][Full Text] [Related]
24. Novel Conjugated Quinazolinone-Based Hydroxamic Acids: Design, Synthesis and Biological Evaluation. Vu TK; Thanh NT; Minh NV; Linh NH; Thao NTP; Nguyen TTB; Hien DT; Chinh LV; Duc TH; Anh LD; Hai PT Med Chem; 2021; 17(7):732-749. PubMed ID: 32310052 [TBL] [Abstract][Full Text] [Related]
25. Design, synthesis, and biological evaluation of indole-based hydroxamic acid derivatives as histone deacetylase inhibitors. Jiang BE; Hu J; Liu H; Liu Z; Wen Y; Liu M; Zhang HK; Pang X; Yu LF Eur J Med Chem; 2022 Jan; 227():113893. PubMed ID: 34656899 [TBL] [Abstract][Full Text] [Related]
26. Design, synthesis and biological evaluation of 4-anilinothieno[2,3-d]pyrimidine-based hydroxamic acid derivatives as novel histone deacetylase inhibitors. Yang W; Li L; Ji X; Wu X; Su M; Sheng L; Zang Y; Li J; Liu H Bioorg Med Chem; 2014 Nov; 22(21):6146-55. PubMed ID: 25261927 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Design, synthesis and evaluation of novel HDAC inhibitors as potential antitumor agents. Cheng J; Qin J; Guo S; Qiu H; Zhong Y Bioorg Med Chem Lett; 2014 Oct; 24(19):4768-4772. PubMed ID: 25182565 [TBL] [Abstract][Full Text] [Related]
30. Development of Purine-Based Hydroxamic Acid Derivatives: Potent Histone Deacetylase Inhibitors with Marked in Vitro and in Vivo Antitumor Activities. Chen Y; Wang X; Xiang W; He L; Tang M; Wang F; Wang T; Yang Z; Yi Y; Wang H; Niu T; Zheng L; Lei L; Li X; Song H; Chen L J Med Chem; 2016 Jun; 59(11):5488-504. PubMed ID: 27186676 [TBL] [Abstract][Full Text] [Related]
31. Development of 3-hydroxycinnamamide-based HDAC inhibitors with potent in vitro and in vivo anti-tumor activity. Li X; Hou J; Li X; Jiang Y; Liu X; Mu W; Jin Y; Zhang Y; Xu W Eur J Med Chem; 2015 Jan; 89():628-37. PubMed ID: 25462271 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Design, synthesis, and biological evaluation of 1, 3-disubstituted-pyrazole derivatives as new class I and IIb histone deacetylase inhibitors. Yao Y; Liao C; Li Z; Wang Z; Sun Q; Liu C; Yang Y; Tu Z; Jiang S Eur J Med Chem; 2014 Oct; 86():639-52. PubMed ID: 25218912 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Design, synthesis and evaluation of novel N-hydroxybenzamides/N-hydroxypropenamides incorporating quinazolin-4(3H)-ones as histone deacetylase inhibitors and antitumor agents. Hieu DT; Anh DT; Tuan NM; Hai PT; Huong LT; Kim J; Kang JS; Vu TK; Dung PTP; Han SB; Nam NH; Hoa ND Bioorg Chem; 2018 Feb; 76():258-267. PubMed ID: 29223029 [TBL] [Abstract][Full Text] [Related]
36. Novel isatin-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents. Nam NH; Huong TL; Dung do TM; Dung PT; Oanh DT; Quyen D; Thao le T; Park SH; Kim KR; Han BW; Yun J; Kang JS; Kim Y; Han SB Eur J Med Chem; 2013; 70():477-86. PubMed ID: 24185378 [TBL] [Abstract][Full Text] [Related]
37. Synthesis, Biological Evaluation, and Computer-Aided Drug Designing of New Derivatives of Hyperactive Suberoylanilide Hydroxamic Acid Histone Deacetylase Inhibitors. Zhang S; Huang W; Li X; Yang Z; Feng B Chem Biol Drug Des; 2015 Oct; 86(4):795-804. PubMed ID: 25763653 [TBL] [Abstract][Full Text] [Related]
38. 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; Mariƫn 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]
39. 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]
40. 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] [Previous] [Next] [New Search]