812653-52-4

Basic information

• Product Name: N-(2-(3-(benzyloxy)-2-methyl-4-oxopyridin-1(4H)-yl)ethyl)-7-methoxy-2-oxo-2H-chromene-3-carboxamide
• Synonyms: N-(2-(3-(benzyloxy)-2-methyl-4-oxopyridin-1(4H)-yl)ethyl)-7-methoxy-2-oxo-2H-chromene-3-carboxamide
• CAS NO: 812653-52-4
• Molecular Weight: 460.486
• Mol File: 812653-52-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(2-(3-(benzyloxy)-2-methyl-4-oxopyridin-1(4H)-yl)ethyl)-7-methoxy-2-oxo-2H-chromene-3-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(3-(benzyloxy)-2-methyl-4-oxopyridin-1(4H)-yl)ethyl)-7-methoxy-2-oxo-2H-chromene-3-carboxamide(812653-52-4)
• EPA Substance Registry System: N-(2-(3-(benzyloxy)-2-methyl-4-oxopyridin-1(4H)-yl)ethyl)-7-methoxy-2-oxo-2H-chromene-3-carboxamide(812653-52-4)

Safety Data

• Hazardous Substances Data: 812653-52-4(Hazardous Substances Data)

Upstream product

• 20300-59-8 7-methoxycoumarin-3-carboxylic acid 
• 149457-89-6 1-(β-aminoethyl)-3-(benzyloxy)-2-methyl-4(1H)-pyridinone 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 6093-72-7 7-methoxycoumarin-3-carboxylic acid ethyl ester 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 61049-69-2 3-O-benzylmaltol 
• 118-71-8 Maltol 

Relevant articles and documents

Rational design, synthesis and biological evaluation of novel multitargeting anti-AD iron chelators with potent MAO-B inhibitory and antioxidant activity

A series of (3-hydroxypyridin-4-one)-coumarin hybrids were developed and investigated as potential multitargeting candidates for the treatment of Alzheimer's disease (AD) through the incorporation of iron-chelating and monoamine oxidase B (MAO-B) inhibition. This combination endowed the hybrids with good capacity to inhibit MAO-B as well as excellent iron-chelating effects. The pFe3+ values of the compounds were ranging from 16.91 to 20.16, comparable to more potent than the reference drug deferiprone (DFP). Among them, compound 18d exhibited the most promising activity against MAO-B, with an IC50 value of 87.9 nM. Moreover, compound 18d exerted favorable antioxidant activity, significantly reversed the amyloid-β1-42 (Aβ1-42) induced PC12 cell damage. More importantly, 18d remarkably ameliorated the cognitive dysfunction in a scopolamine-induced mice AD model. In brief, a series of hybrids with potential anti-AD effect were successfully obtained, indicating that the design of iron chelators with MAO-B inhibitory and antioxidant activities is an attractive strategy against AD progression.