Rapid synthesis of flavone-based monoamine oxidase (MAO) inhibitors targeting two active sites using click chemistry-Reference-Cited by-同舟云学术

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Rapid synthesis of flavone-based monoamine oxidase (MAO) inhibitors targeting two active sites using click chemistry

Published:2016-09-26 Issue:1 Volume:89 Page:141-151
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Jia Wei Zhen¹,Cheng Feng¹,Zhang Yin Jun¹,Ge Jin Yan¹,Yao Shao Q.²,Zhu Qing¹

Affiliation:

1. Institute of Bioengineering; Zhejiang University of Technology; Zhejiang China

2. Department of Chemistry; National University of Singapore; Singapore Singapore

Funder

National Natural Science Foundation of China

Project of Science Technology Department of Zhejiang Province

Project of Science Technology Department of Jinhua City

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cbdd.12841/fullpdf

Reference51 articles.

1. MONOAMINE OXIDASE: From Genes to Behavior

2. The functional role of monoamine oxidases A and B in the mammalian central nervous system

3. Structure and Mechanism of Monoamine Oxidase

4. Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders

5. Interactions of Nitrogen-Containing Xenobiotics with Monoamine Oxidase (MAO) Isozymes A and B: SAR Studies on MAO Substrates and Inhibitors

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1. “Click Chemistry”: An Emerging Tool for Developing a New Class of Structural Motifs against Various Neurodegenerative Disorders;ACS Omega;2023-11-14

2. Monoamine oxidase B inhibitors based on natural privileged scaffolds: A review of systematically structural modification;International Journal of Biological Macromolecules;2023-11

3. Structure-Based Design of Novel MAO-B Inhibitors: A Review;Molecules;2023-06-16

4. Recent advancements in chromone as a privileged scaffold towards the development of small molecules for neurodegenerative therapeutics;RSC Medicinal Chemistry;2022

5. “Click” assembly of novel dual inhibitors of AChE and MAO-B from pyridoxine derivatives for the treatment of Alzheimer’s disease;Heterocyclic Communications;2022-01-01

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