Design and Synthesis of C3-Substituted β-Carboline-Based Histone Deacetylase Inhibitors with Potent Antitumor Activities-Reference-Cited by-同舟云学术

Design and Synthesis of C3-Substituted β-Carboline-Based Histone Deacetylase Inhibitors with Potent Antitumor Activities

Author:

Ling Yong¹²,Feng Jiao¹,Luo Lin¹,Guo Jing¹,Peng Yanfu¹,Wang Tingting¹,Ge Xiang¹,Xu Qibing¹,Wang Xinyang¹²,Dai Hong¹³,Zhang Yanan¹

Affiliation:

1. School of Pharmacy and Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Targets; Nantong University; Nantong 226001 P.R. China

2. State Key Laboratory of Natural Medicines; China Pharmaceutical University; Nanjing 210009 P.R. China

3. College of Chemistry and Chemical Engineering; Nantong University; Nantong 226001 P.R. China

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Reference36 articles.

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