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.
2. Design and biological evaluation of tetrahydro-β-carboline derivatives as highly potent histone deacetylase 6 (HDAC6) inhibitors. Leonhardt M; Sellmer A; Krämer OH; Dove S; Elz S; Kraus B; Beyer M; Mahboobi S Eur J Med Chem; 2018 May; 152():329-357. PubMed ID: 29738953 [TBL] [Abstract][Full Text] [Related]
3. Design, synthesis and biological evaluation of 3, 4-disubstituted-imidazolidine-2, 5-dione derivatives as HDAC6 selective inhibitors. Liang T; Xue J; Yao Z; Ye Y; Yang X; Hou X; Fang H Eur J Med Chem; 2021 Oct; 221():113526. PubMed ID: 33992929 [TBL] [Abstract][Full Text] [Related]
4. Development of selective HDAC6 inhibitors with in vitro and in vivo anti-multiple myeloma activity. Li S; Zhao C; Zhang G; Xu Q; Liu Q; Zhao W; James Chou C; Zhang Y Bioorg Chem; 2021 Nov; 116():105278. PubMed ID: 34474303 [TBL] [Abstract][Full Text] [Related]
5. Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 Inhibitors. Vögerl K; Ong N; Senger J; Herp D; Schmidtkunz K; Marek M; Müller M; Bartel K; Shaik TB; Porter NJ; Robaa D; Christianson DW; Romier C; Sippl W; Jung M; Bracher F J Med Chem; 2019 Feb; 62(3):1138-1166. PubMed ID: 30645113 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Inhibitors of histone deacetylase 6 based on a novel 3-hydroxy-isoxazole zinc binding group. Linciano P; Pinzi L; Belluti S; Chianese U; Benedetti R; Moi D; Altucci L; Franchini S; Imbriano C; Sorbi C; Rastelli G J Enzyme Inhib Med Chem; 2021 Dec; 36(1):2080-2086. PubMed ID: 34583596 [TBL] [Abstract][Full Text] [Related]
9. Novel pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione (PBD) derivatives as selective HDAC6 inhibitors to suppress tumor metastasis and invasion in vitro and in vivo. Li Y; Quan J; Song H; Li D; Ma E; Wang Y; Ma C Bioorg Chem; 2021 Sep; 114():105081. PubMed ID: 34153811 [TBL] [Abstract][Full Text] [Related]
10. Enantioselective synthesis and biological investigation of tetrahydro-β-carboline-based HDAC6 inhibitors with improved solubility. Grünstein E; Sellmer A; Mahboobi S Arch Pharm (Weinheim); 2019 Jun; 352(6):e1900026. PubMed ID: 31056792 [TBL] [Abstract][Full Text] [Related]
11. Discovery of a potent histone deacetylase (HDAC) 3/6 selective dual inhibitor. Soumyanarayanan U; Ramanujulu PM; Mustafa N; Haider S; Fang Nee AH; Tong JX; Tan KSW; Chng WJ; Dymock BW Eur J Med Chem; 2019 Dec; 184():111755. PubMed ID: 31627059 [TBL] [Abstract][Full Text] [Related]
12. PTG-0861: A novel HDAC6-selective inhibitor as a therapeutic strategy in acute myeloid leukaemia. Gawel JM; Shouksmith AE; Raouf YS; Nawar N; Toutah K; Bukhari S; Manaswiyoungkul P; Olaoye OO; Israelian J; Radu TB; Cabral AD; Sina D; Sedighi A; de Araujo ED; Gunning PT Eur J Med Chem; 2020 Sep; 201():112411. PubMed ID: 32615502 [TBL] [Abstract][Full Text] [Related]
14. Identification of novel 1,3-diaryl-1,2,4-triazole-capped histone deacetylase 6 inhibitors with potential anti-gastric cancer activity. Zhang XH; Kang HQ; Tao YY; Li YH; Zhao JR; Ya-Gao ; Ma LY; Liu HM Eur J Med Chem; 2021 Jun; 218():113392. PubMed ID: 33831778 [TBL] [Abstract][Full Text] [Related]
15. Biological and structural investigation of tetrahydro-β-carboline-based selective HDAC6 inhibitors with improved stability. Scheuerer S; Motlova L; Schäker-Hübner L; Sellmer A; Feller F; Ertl FJ; Koch P; Hansen FK; Barinka C; Mahboobi S Eur J Med Chem; 2024 Oct; 276():116676. PubMed ID: 39067437 [TBL] [Abstract][Full Text] [Related]
16. Novel 2, 5-diketopiperazine derivatives as potent selective histone deacetylase 6 inhibitors: Rational design, synthesis and antiproliferative activity. Chen X; Chen X; Steimbach RR; Wu T; Li H; Dan W; Shi P; Cao C; Li D; Miller AK; Qiu Z; Gao J; Zhu Y Eur J Med Chem; 2020 Feb; 187():111950. PubMed ID: 31865013 [TBL] [Abstract][Full Text] [Related]
17. Multicomponent Synthesis, Binding Mode, and Structure-Activity Relationship of Selective Histone Deacetylase 6 (HDAC6) Inhibitors with Bifurcated Capping Groups. Reßing N; Sönnichsen M; Osko JD; Schöler A; Schliehe-Diecks J; Skerhut A; Borkhardt A; Hauer J; Kassack MU; Christianson DW; Bhatia S; Hansen FK J Med Chem; 2020 Sep; 63(18):10339-10351. PubMed ID: 32803970 [TBL] [Abstract][Full Text] [Related]
18. Combined Ligand and Fragment-based Drug Design of Selective Histone Deacetylase - 6 Inhibitors. Ruzic D; Petkovic M; Agbaba D; Ganesan A; Nikolic K Mol Inform; 2019 May; 38(5):e1800083. PubMed ID: 30632697 [TBL] [Abstract][Full Text] [Related]
19. Carboxylic acid derivatives display potential selectivity for human histone deacetylase 6: Structure-based virtual screening, molecular docking and dynamics simulation studies. Uba AI; Yelekçi K Comput Biol Chem; 2018 Aug; 75():131-142. PubMed ID: 29859380 [TBL] [Abstract][Full Text] [Related]
20. Development of Thiazolidinedione-Based HDAC6 Inhibitors to Overcome Methamphetamine Addiction. Sharma C; Oh YJ; Park B; Lee S; Jeong CH; Lee S; Seo JH; Seo YH Int J Mol Sci; 2019 Dec; 20(24):. PubMed ID: 31835389 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]