Synthesis and Biological Assessment of Racemic Benzochromenopyrimidinimines as Antioxidant, Cholinesterase, and Aβ1-42 Aggregation Inhibitors for Alzheimer's Disease Therapy.
CHEMMEDCHEM(2016)
Abstract
Given the complex nature of Alzheimer's disease (AD), compounds that are able to simultaneously address two or more AD-associated targets show greater promise for development into drugs for AD therapy. Herein we report an efficient two-step synthesis and biological evaluation of new racemic benzochromene derivatives as antioxidants, inhibitors of cholinesterase and beta-amyloid (A beta(1-42)) aggregation. Based on the results of the primary screening, we identified 15-(3-methoxyphenyl)-9,11,12,15-tetrahydro-10H,14H-benzo[5,6]chromeno[2,3-d]pyrido[1,2-a]pyrimidin-14-imine (3e) and 16-(3-methoxyphenyl)-9,10,11,12,13,16-hexahydro-15H-benzo[5',6']chromeno[2',3':4,5]pyrimido[1,2-a]azepin-15-imine (3 f) as new potential multitarget-directed ligands for AD therapy. Further indepth biological analysis showed that compound 3 f is a good human acetylcholinesterase inhibitor [IC50=(0.36 +/- 0.02) mu m], has strong antioxidant activity (3.61 mu mol Trolox equivalents), and moderate A beta(1-42) antiaggregating power (40.3%).
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Key words
Alzheimer's disease,antioxidants,inhibitors,molecular modeling,multitarget-directed ligands
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