Synthesis and activity of miconazole derivatives as dual BChE/IDO1 inhibitors for the treatment of Alzheimer's disease

Author:

Lu Xin1,Liu Yijun1,Qin Nan2,Yang Hongyu1,Qiao Yuting1,Jiang Xueyang2,Chen Yao3,Feng Feng42,Liu Wenyuan1,Zhou You5,Sun Haopeng14

Affiliation:

1. School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China

2. Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, 211198, China

3. School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China

4. Jiangsu Food & Pharmaceutical Science College, Huaian, 223003, China

5. College of Sericulture, Textile and Biomass Sciences, Southwest University, Chongqing, 400715, China

Abstract

Background: Alzheimer's disease is a multifactorial neurological disorder seen in elderly people. Loss of cholinergic transmission and unbalanced tryptophan metabolism kynurenine pathway have been demonstrated in neuropsychiatric diseases. Methods & results: Among the two series of synthesized compounds, compounds 5c and 5h were identified as effective dual BChE/IDO1 inhibitors, with well-balanced micromolar activity. Compounds 5c and 5h exhibited promising ability to ameliorate behavioral impairment by Morris water maze. The safety of miconazole analogs was also validated by PC12 and SH-SY5Y cell lines. Conclusion: These results highlight the ability of 5c and 5h to treat Alzheimer's disease.

Funder

Fundamental Research Funds for the Central Universities

“Double First-Class” initiative Innovation team project of China Pharmaceutical University

National Natural Science Foundation of China

Basic Research and Frontier Exploration Project of Chongqing

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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