Identification of 4-aminoquinoline core for the design of new cholinesterase inhibitors

Author:

Chen Yao12,Bian Yaoyao3,Sun Yuan4,Kang Chen5,Yu Sheng1,Fu Tingming12,Li Wei1,Pei Yuqiong1,Sun Haopeng6

Affiliation:

1. School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China

2. Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, Nanjing, China

3. School of Nursing, Nanjing University of Chinese Medicine, Nanjing, China

4. Department of Chemistry and Biochemistry, Ohio State University, Columbus, OH, United States

5. Division of Pharmacology, College of Pharmacy, Ohio State University, Columbus, OH, United States

6. Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing, China

Abstract

Inhibition of acetylcholinesterase (AChE) using small molecules is still one of the most successful therapeutic strategies in the treatment of Alzheimer’s disease (AD). Previously we reported compound T5369186 with a core of quinolone as a new cholinesterase inhibitor. In the present study, in order to identify new cores for the designing of AChE inhibitors, we screened different derivatives of this core with the aim to identify the best core as the starting point for further optimization. Based on the results, we confirmed that only 4-aminoquinoline (compound 04 and 07) had cholinesterase inhibitory effects. Considering the simple structure and high inhibitory potency against AChE, 4-aminoquinoline provides a good starting core for further designing novel multifunctional AChEIs.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Top-notch Academic Programs Project of Jiangsu Higher Education Institutions

Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference22 articles.

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2. Alzheimer disease;Castellani;Disease-a-Month,2010

3. Discovery of new acetylcholinesterase inhibitors with small core structures through shape-based virtual screening;Chen;Bioorganic & Medicinal Chemistry Letters,2015

4. Recent developments in fragment-based drug discovery;Congreve;Journal of Medicinal Chemistry,2008

5. Small molecule blockers of the Alzheimer Abeta calcium channel potently protect neurons from Abeta cytotoxicity;Diaz;Proceedings of the National Academy of Sciences of the United States of America,2009

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