4.7 Article

Synthesis and pharmacological evaluation of novel chromone derivatives as balanced multifunctional agents against Alzheimer's disease

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 25, Issue 14, Pages 3815-3826

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2017.05.027

Keywords

Alzheimer's disease; Chromone; Monoamine oxidase; Metal chelator; The blood-brain barrier

Funding

  1. National Natural Science Foundation of China [81573313]
  2. Innovative Research Team in University [IRT_15R63]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

Ask authors/readers for more resources

In a continuing effort to develop multitargeted compounds as potential treatment agents against Alzheimer's disease (AD), a series of chromone derivatives were designed, synthesized and evaluated. In vitro assay indicated that most of the target compounds have both MAOs inhibition activities, antioxidant activity and biometal chelating ability. Especially, compound s19 exhibits good inhibitory potency for inhibition of MAOs (IC50 value of 5.12 mu M for hMAO-A and 0.816 mu M for hMAO-B), moderate inhibition of A beta aggregation (75.1% at 20 mu M), metal chelation, control of ROS generation and antioxidant activity (ORAC = 3.62). In addition, s19 could reduce P02 cells death induced by oxidative stress and penetrate the blood-brain barrier (BBB). Taken together, these results suggested that s19 might be a promising multitargeted compound for AD treatment. (C) 2017 Published by Elsevier Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available