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.
132 related articles for article (PubMed ID: 34954594)
1. Design and synthesis of HDAC inhibitors to enhance the therapeutic effect of diffuse large B-cell lymphoma by improving metabolic stability and pharmacokinetic characteristics. Cui H; Hong Q; Wei R; Li H; Wan C; Chen X; Zhao S; Bu H; Zhang B; Yang D; Lu T; Chen Y; Zhu Y Eur J Med Chem; 2022 Feb; 229():114049. PubMed ID: 34954594 [TBL] [Abstract][Full Text] [Related]
2. Preclinical evaluation and molecular docking of 1,3-benzodioxole propargyl ether derivatives as novel inhibitor for combating the histone deacetylase enzyme in cancer. Kumar N; Tomar R; Pandey A; Tomar V; Singh VK; Chandra R Artif Cells Nanomed Biotechnol; 2018 Sep; 46(6):1288-1299. PubMed ID: 28847179 [TBL] [Abstract][Full Text] [Related]
4. Discovery of 1,2,4-oxadiazole-Containing hydroxamic acid derivatives as histone deacetylase inhibitors potential application in cancer therapy. Yang Z; Shen M; Tang M; Zhang W; Cui X; Zhang Z; Pei H; Li Y; Hu M; Bai P; Chen L Eur J Med Chem; 2019 Sep; 178():116-130. PubMed ID: 31177073 [TBL] [Abstract][Full Text] [Related]
5. Discovery of Novel Janus Kinase (JAK) and Histone Deacetylase (HDAC) Dual Inhibitors for the Treatment of Hematological Malignancies. Liang X; Zang J; Li X; Tang S; Huang M; Geng M; Chou CJ; Li C; Cao Y; Xu W; Liu H; Zhang Y J Med Chem; 2019 Apr; 62(8):3898-3923. PubMed ID: 30901208 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Design, synthesis, and biological evaluation of novel histone deacetylase 1 inhibitors through click chemistry. Sun Q; Yao Y; Liu C; Li H; Yao H; Xue X; Liu J; Tu Z; Jiang S Bioorg Med Chem Lett; 2013 Jun; 23(11):3295-9. PubMed ID: 23601706 [TBL] [Abstract][Full Text] [Related]
9. Discovery of Thieno[2,3- Pan Z; Li X; Wang Y; Jiang Q; Jiang L; Zhang M; Zhang N; Wu F; Liu B; He G J Med Chem; 2020 Apr; 63(7):3678-3700. PubMed ID: 32153186 [TBL] [Abstract][Full Text] [Related]
10. Design, synthesis and biological evaluation of novel histone deacetylase inhibitors incorporating 4-aminoquinazolinyl systems as capping groups. Zhang Q; Li Y; Zhang B; Lu B; Li J Bioorg Med Chem Lett; 2017 Nov; 27(21):4885-4888. PubMed ID: 28947154 [TBL] [Abstract][Full Text] [Related]
11. Discovery of pyridone-based histone deacetylase inhibitors: approaches for metabolic stability. Cho M; Choi E; Yang JS; Lee C; Seo JJ; Kim BS; Oh SJ; Kim HM; Lee K; Park SK; Kwon HJ; Han G ChemMedChem; 2013 Feb; 8(2):272-9. PubMed ID: 23292995 [TBL] [Abstract][Full Text] [Related]
12. Design, Synthesis and Biological Evaluation of Novel Coumarin-Based Hydroxamate Derivatives as Histone Deacetylase (Hdac) Inhibitors with Antitumor Activities. Yang F; Zhao N; Song J; Zhu K; Jiang CS; Shan P; Zhang H Molecules; 2019 Jul; 24(14):. PubMed ID: 31311163 [TBL] [Abstract][Full Text] [Related]
13. Discovery of STAT3 and Histone Deacetylase (HDAC) Dual-Pathway Inhibitors for the Treatment of Solid Cancer. Ren Y; Li S; Zhu R; Wan C; Song D; Zhu J; Cai G; Long S; Kong L; Yu W J Med Chem; 2021 Jun; 64(11):7468-7482. PubMed ID: 34043359 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Synthesis and biological characterization of amidopropenyl hydroxamates as HDAC inhibitors. Thaler F; Varasi M; Colombo A; Boggio R; Munari D; Regalia N; Rozio MG; Reali V; Resconi AE; Mai A; Gagliardi S; Dondio G; Minucci S; Mercurio C ChemMedChem; 2010 Aug; 5(8):1359-72. PubMed ID: 20572281 [TBL] [Abstract][Full Text] [Related]
16. Thioether-based 2-aminobenzamide derivatives: Novel HDAC inhibitors with potent in vitro and in vivo antitumor activity. Yun F; Cheng C; Ullah S; He J; Zahi MR; Yuan Q Eur J Med Chem; 2019 Aug; 176():195-207. PubMed ID: 31103900 [TBL] [Abstract][Full Text] [Related]
17. Design, synthesis and biological evaluation of novel c-Met/HDAC dual inhibitors. Dong Y; Hu H; Sun Y; Qin M; Gong P; Hou Y; Zhao Y Bioorg Med Chem Lett; 2020 Dec; 30(23):127610. PubMed ID: 33045329 [TBL] [Abstract][Full Text] [Related]
19. Cysteine derivatives as acetyl lysine mimics to inhibit zinc-dependent histone deacetylases for treating cancer. Wang J; Cao Z; Wang F; Wang P; An J; Fu X; Liu T; Li Y; Li Y; Zhao Y; Lin H; He B Eur J Med Chem; 2021 Dec; 225():113799. PubMed ID: 34500130 [TBL] [Abstract][Full Text] [Related]
20. Discovery of 2,4-pyrimidinediamine derivatives as potent dual inhibitors of ALK and HDAC. Pan T; Dan Y; Guo D; Jiang J; Ran D; Zhang L; Tian B; Yuan J; Yu Y; Gan Z Eur J Med Chem; 2021 Nov; 224():113672. PubMed ID: 34237620 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]