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.
117 related articles for article (PubMed ID: 39047608)
1. Design, synthesis, and biological activity evaluation of novel HDAC3 selective inhibitors for combination with Venetoclax against acute myeloid leukemia. Liu E; Chen Y; Qin M; Yue K; Sun S; Jiang Y; Li X Eur J Med Chem; 2024 Oct; 276():116663. PubMed ID: 39047608 [TBL] [Abstract][Full Text] [Related]
2. Synthesis, biological evaluation, and molecular docking analysis of novel linker-less benzamide based potent and selective HDAC3 inhibitors. Routholla G; Pulya S; Patel T; Abdul Amin S; Adhikari N; Biswas S; Jha T; Ghosh B Bioorg Chem; 2021 Sep; 114():105050. PubMed ID: 34120025 [TBL] [Abstract][Full Text] [Related]
3. Marine Cytotoxin Santacruzamate A Derivatives as Potent HDAC1-3 Inhibitors and Their Synergistic Anti-Leukemia Effects with Venetoclax. Hao W; Wang L; Xu T; Jia G; Jiang Y; Qin C; Li X Mar Drugs; 2024 May; 22(6):. PubMed ID: 38921561 [TBL] [Abstract][Full Text] [Related]
4. Design, synthesis and binding mode of interaction of novel small molecule o-hydroxy benzamides as HDAC3-selective inhibitors with promising antitumor effects in 4T1-Luc breast cancer xenograft model. Routholla G; Pulya S; Patel T; Adhikari N; Abdul Amin S; Paul M; Bhagavatula S; Biswas S; Jha T; Ghosh B Bioorg Chem; 2021 Dec; 117():105446. PubMed ID: 34717237 [TBL] [Abstract][Full Text] [Related]
5. Discovery of novel class of histone deacetylase inhibitors as potential anticancer agents. El-Awady R; Saleh E; Hamoudi R; Ramadan WS; Mazitschek R; Nael MA; Elokely KM; Abou-Gharbia M; Childers WE; Srinivasulu V; Aloum L; Menon V; Al-Tel TH Bioorg Med Chem; 2021 Jul; 42():116251. PubMed ID: 34116381 [TBL] [Abstract][Full Text] [Related]
6. Design, Synthesis, Molecular Modeling, and Biological Evaluation of Novel Amine-based Histone Deacetylase Inhibitors. Abdelkarim H; Neelarapu R; Madriaga A; Vaidya AS; Kastrati I; Karumudi B; Wang YT; Taha TY; Thatcher GRJ; Frasor J; Petukhov PA ChemMedChem; 2017 Dec; 12(24):2030-2043. PubMed ID: 29080240 [TBL] [Abstract][Full Text] [Related]
7. Design, synthesis and biological evaluation of novel 2-aminobenzamides containing dithiocarbamate moiety as histone deacetylase inhibitors and potent antitumor agents. Xie R; Li Y; Tang P; Yuan Q Eur J Med Chem; 2018 Jan; 143():320-333. PubMed ID: 29202397 [TBL] [Abstract][Full Text] [Related]
8. Targeting epigenetic reader and eraser: Rational design, synthesis and in vitro evaluation of dimethylisoxazoles derivatives as BRD4/HDAC dual inhibitors. Zhang Z; Hou S; Chen H; Ran T; Jiang F; Bian Y; Zhang D; Zhi Y; Wang L; Zhang L; Li H; Zhang Y; Tang W; Lu T; Chen Y Bioorg Med Chem Lett; 2016 Jun; 26(12):2931-2935. PubMed ID: 27142751 [TBL] [Abstract][Full Text] [Related]
9. Design, synthesis and biological evaluation of novel thioquinazolinone-based 2-aminobenzamide derivatives as potent histone deacetylase (HDAC) inhibitors. Cheng C; Yun F; He J; Ullah S; Yuan Q Eur J Med Chem; 2019 Jul; 173():185-202. PubMed ID: 31003060 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Design, synthesis and biological evaluation of novel isoindolinone derivatives as potent histone deacetylase inhibitors. Chen X; Zhao S; Li H; Wang X; Geng A; Cui H; Lu T; Chen Y; Zhu Y Eur J Med Chem; 2019 Apr; 168():110-122. PubMed ID: 30802729 [TBL] [Abstract][Full Text] [Related]
12. Targeting breast cancer stem cells by novel HDAC3-selective inhibitors. Hsieh HY; Chuang HC; Shen FH; Detroja K; Hsin LW; Chen CS Eur J Med Chem; 2017 Nov; 140():42-51. PubMed ID: 28923385 [TBL] [Abstract][Full Text] [Related]
13. Novel inhibitors of human histone deacetylases: design, synthesis and bioactivity of 3-alkenoylcoumarines. Seidel C; Schnekenburger M; Zwergel C; Gaascht F; Mai A; Dicato M; Kirsch G; Valente S; Diederich M Bioorg Med Chem Lett; 2014 Aug; 24(16):3797-801. PubMed ID: 25042254 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. β-Carboline tethered cinnamoyl 2-aminobenzamides as class I selective HDAC inhibitors: Design, synthesis, biological activities and modelling studies. Namballa HK; Anchi P; Lakshmi Manasa K; Soni JP; Godugu C; Shankaraiah N; Kamal A Bioorg Chem; 2021 Dec; 117():105461. PubMed ID: 34753060 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Novel Pyridine-Based Hydroxamates and 2'-Aminoanilides as Histone Deacetylase Inhibitors: Biochemical Profile and Anticancer Activity. Zwergel C; Di Bello E; Fioravanti R; Conte M; Nebbioso A; Mazzone R; Brosch G; Mercurio C; Varasi M; Altucci L; Valente S; Mai A ChemMedChem; 2021 Mar; 16(6):989-999. PubMed ID: 33220015 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]