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.
266 related articles for article (PubMed ID: 23964961)
1. Potent histone deacetylase inhibitors derived from 4-(aminomethyl)-N-hydroxybenzamide with high selectivity for the HDAC6 isoform. Blackburn C; Barrett C; Chin J; Garcia K; Gigstad K; Gould A; Gutierrez J; Harrison S; Hoar K; Lynch C; Rowland RS; Tsu C; Ringeling J; Xu H J Med Chem; 2013 Sep; 56(18):7201-11. PubMed ID: 23964961 [TBL] [Abstract][Full Text] [Related]
2. Histone deacetylase inhibitors derived from 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine and related heterocycles selective for the HDAC6 isoform. Blackburn C; Barrett C; Brunson M; Chin J; England D; Garcia K; Gigstad K; Gould A; Gutierrez J; Hoar K; Rowland RS; Tsu C; Ringeling J; Wager K; Xu H Bioorg Med Chem Lett; 2014 Dec; 24(23):5450-4. PubMed ID: 25454270 [TBL] [Abstract][Full Text] [Related]
3. Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif. Wagner FF; Olson DE; Gale JP; Kaya T; Weïwer M; Aidoud N; Thomas M; Davoine EL; Lemercier BC; Zhang YL; Holson EB J Med Chem; 2013 Feb; 56(4):1772-6. PubMed ID: 23368884 [TBL] [Abstract][Full Text] [Related]
4. Discovery of the first histone deacetylase 6/8 dual inhibitors. Olson DE; Wagner FF; Kaya T; Gale JP; Aidoud N; Davoine EL; Lazzaro F; Weïwer M; Zhang YL; Holson EB J Med Chem; 2013 Jun; 56(11):4816-20. PubMed ID: 23672185 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. New aryldithiolethione derivatives as potent histone deacetylase inhibitors. Tazzari V; Cappelletti G; Casagrande M; Perrino E; Renzi L; Del Soldato P; Sparatore A Bioorg Med Chem; 2010 Jun; 18(12):4187-94. PubMed ID: 20576572 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Synthesis of benzothiophene-based hydroxamic acids as potent and selective HDAC6 inhibitors. De Vreese R; Van Steen N; Verhaeghe T; Desmet T; Bougarne N; De Bosscher K; Benoy V; Haeck W; Van Den Bosch L; D'hooghe M Chem Commun (Camb); 2015 Jun; 51(48):9868-71. PubMed ID: 25994553 [TBL] [Abstract][Full Text] [Related]
13. Alkyl piperidine and piperazine hydroxamic acids as HDAC inhibitors. Rossi C; Porcelloni M; D'Andrea P; Fincham CI; Ettorre A; Mauro S; Squarcia A; Bigioni M; Parlani M; Nardelli F; Binaschi M; Maggi CA; Fattori D Bioorg Med Chem Lett; 2011 Apr; 21(8):2305-8. PubMed ID: 21420859 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Discovery of potent, isoform-selective inhibitors of histone deacetylase containing chiral heterocyclic capping groups and a N-(2-aminophenyl)benzamide binding unit. Marson CM; Matthews CJ; Yiannaki E; Atkinson SJ; Soden PE; Shukla L; Lamadema N; Thomas NS J Med Chem; 2013 Aug; 56(15):6156-74. PubMed ID: 23829483 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Design, synthesis, and biological evaluation of 2-aminobenzanilide derivatives as potent and selective HDAC inhibitors. Stolfa DA; Stefanachi A; Gajer JM; Nebbioso A; Altucci L; Cellamare S; Jung M; Carotti A ChemMedChem; 2012 Jul; 7(7):1256-66. PubMed ID: 22628266 [TBL] [Abstract][Full Text] [Related]
20. The structural requirements of histone deacetylase inhibitors: SAHA analogs modified at the C5 position display dual HDAC6/8 selectivity. Negmeldin AT; Pflum MKH Bioorg Med Chem Lett; 2017 Aug; 27(15):3254-3258. PubMed ID: 28648461 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]