Synthesis and biological evaluation of phenothiazine derivative-containing hydroxamic acids as potent class II histone deacetylase inhibitors

European Journal of Medicinal Chemistry ◽

10.1016/j.ejmech.2021.113419 ◽

2021 ◽

Vol 219 ◽

pp. 113419

Author(s):

Kai-Cheng Hsu ◽

Jung-Chun Chu ◽

Hui-Ju Tseng ◽

Chia-I Liu ◽

Hao-Ching Wang ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Class Ii ◽

Hydroxamic Acids ◽

Biological Evaluation ◽

Phenothiazine Derivative ◽

Synthesis And Biological Evaluation

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Class II (IIa)-Selective Histone Deacetylase Inhibitors. 1. Synthesis and Biological Evaluation of Novel (Aryloxopropenyl)pyrrolyl Hydroxyamides

Journal of Medicinal Chemistry ◽

10.1021/jm049002a ◽

2005 ◽

Vol 48 (9) ◽

pp. 3344-3353 ◽

Author(s):

Antonello Mai ◽

Silvio Massa ◽

Riccardo Pezzi ◽

Silvia Simeoni ◽

Dante Rotili ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Class Ii ◽

Biological Evaluation ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of di-substituted cinnamic hydroxamic acids bearing urea/thiourea unit as potent histone deacetylase inhibitors

Bioorganic & Medicinal Chemistry Letters ◽

10.1016/j.bmcl.2013.09.051 ◽

2013 ◽

Vol 23 (23) ◽

pp. 6432-6435 ◽

Author(s):

Chengqing Ning ◽

Yanjing Bi ◽

Yujun He ◽

WenYuan Huang ◽

Lifei Liu ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Hydroxamic Acids ◽

Biological Evaluation ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation

ACS Omega ◽

10.1021/acsomega.0c05870 ◽

2021 ◽

Vol 6 (7) ◽

pp. 4907-4920

Author(s):

Duong T. Anh ◽

Pham-The Hai ◽

Le D. Huy ◽

Hoang B. Ngoc ◽

Trinh T. M. Ngoc ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Synthesis and biological evaluation of acridine-based histone deacetylase inhibitors as multitarget agents against Alzheimer’s disease

European Journal of Medicinal Chemistry ◽

10.1016/j.ejmech.2020.112193 ◽

2020 ◽

Vol 192 ◽

pp. 112193 ◽

Author(s):

Hui-Ju Tseng ◽

Mei-Hsiang Lin ◽

Young-Ji Shiao ◽

Ying-Chen Yang ◽

Jung-Chun Chu ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Synthesis And Biological Evaluation

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Design, synthesis, and biological evaluation of novel 2,4-thiazolidinedione derivatives as histone deacetylase inhibitors targeting liver cancer cell line

Medicinal Chemistry Research ◽

10.1007/s00044-011-9623-3 ◽

2011 ◽

Vol 21 (7) ◽

pp. 1156-1165 ◽

Author(s):

Rhea Mohan ◽

Ajit K. Sharma ◽

Sanjay Gupta ◽

C. S. Ramaa

Keyword(s):

Liver Cancer ◽

Cell Line ◽

Histone Deacetylase ◽

Cancer Cell ◽

Histone Deacetylase Inhibitors ◽

Cancer Cell Line ◽

Biological Evaluation ◽

Liver Cancer Cell ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of 4-piperidin-4-yl-triazole derivatives as novel histone deacetylase inhibitors

BioScience Trends ◽

10.5582/bst.2019.01055 ◽

2019 ◽

Vol 13 (2) ◽

pp. 197-203 ◽

Author(s):

He Miao ◽

Jianjun Gao ◽

Zishuo Mou ◽

Baolei Wang ◽

Li Zhang ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Design Synthesis ◽

Triazole Derivatives ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of coumarin-based N-hydroxycinnamamide derivatives as novel histone deacetylase inhibitors with anticancer activities

Bioorganic Chemistry ◽

10.1016/j.bioorg.2020.104023 ◽

2020 ◽

Vol 101 ◽

pp. 104023 ◽

Author(s):

Jiaoli Ding ◽

Jing Liu ◽

Zhipeng Zhang ◽

Jie Guo ◽

Maojun Cheng ◽

...

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Anticancer Activities ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of novel 2-aminobenzamides containing dithiocarbamate moiety as histone deacetylase inhibitors and potent antitumor agents

European Journal of Medicinal Chemistry ◽

10.1016/j.ejmech.2017.08.041 ◽

2018 ◽

Vol 143 ◽

pp. 320-333 ◽

Author(s):

Rui Xie ◽

Yan Li ◽

Pingwah Tang ◽

Qipeng Yuan

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Antitumor Agents ◽

Biological Evaluation ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of novel histone deacetylase inhibitors based on virtual screening

Acta Pharmaceutica Sinica B ◽

10.1016/j.apsb.2011.10.002 ◽

2011 ◽

Vol 1 (4) ◽

pp. 240-247 ◽

Author(s):

Hui Lu ◽

Ya-dong Chen ◽

Bo Yang ◽

Qi-dong You

Keyword(s):

Virtual Screening ◽

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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Design, synthesis and biological evaluation of indeno[1,2-d]thiazole derivatives as potent histone deacetylase inhibitors

Bioorganic & Medicinal Chemistry Letters ◽

10.1016/j.bmcl.2013.04.004 ◽

2013 ◽

Vol 23 (11) ◽

pp. 3200-3203 ◽

Author(s):

Ming Zhou ◽

Chengqing Ning ◽

Ruihuan Liu ◽

Yujun He ◽

Niefang Yu

Keyword(s):

Histone Deacetylase ◽

Histone Deacetylase Inhibitors ◽

Biological Evaluation ◽

Thiazole Derivatives ◽

Design Synthesis ◽

Synthesis And Biological Evaluation

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