898045-01-7

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 118708-61-5 5-p-methoxybenzyloxy-2-hydroxymethyl-4-pyrone 
• 501-30-4 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one 
• 898045-00-6 (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate 

Downstream Products

• 898045-02-8 dimethyl (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methylphosphonate 
• 1381864-88-5 5-(4-methoxybenzyloxy)-2-((quinolin-8-yloxy)methyl)-4H-pyran-4-one 
• 1381864-98-7 diethyl ((5-((4-methoxybenzyl)oxy)-4-oxo-4H-pyran-2-yl)methyl)phosphonate 
• 1443302-28-0 2-(((4-chlorophenyl)thio)methyl)-5-((4-methoxybenzyl)oxy)-4H-pyran-4-one 
• 1443302-43-9 5-(4-methoxybenzyloxy)-2-((pyrimidin-2-ylthio)methyl)-4H-pyran-4-one 
• 1443302-19-9 5-(4-methoxybenzyloxy)-2-((naphthalen-2-yloxy)methyl)-4H-pyran-4-one 
• 1443302-17-7 5-(4-methoxybenzyloxy)-2-((naphthalen-1-yloxy)methyl)-4H-pyran-4-one 
• 898045-04-0 C₂₈H₂₄O₈ 

Relevant academic research and scientific papers

D-AMINO ACID OXIDASE INHIBITORS AND THERAPEUTIC USES THEREOF

The present invention relates to compounds of Formula (I): or a pharmaceutically acceptable salt thereof, wherein: each of A, B, C, D, and E, independently, is C, N, N—H, O, S, or absent is a single bond or a double bond; each of X, Y, and Z, independentl

Synthesis of kojic acid-derived copper-chelating apoptosis inducing agents

Three classes of kojic acid derivatives were synthesized and examined for their antiproliferative activity against HeLa cells. Both 8b and 11 co-treated with copper ion exhibited synergistic effect on the HeLa cell growth inhibition with GI50 v

Synthesis of kojic acid derivatives as secondary binding site probes of d-amino acid oxidase

A series of kojic acid (5-hydroxy-2-hydroxymethyl-4H-pyran-4-one) derivatives were synthesized and tested for their ability to inhibit d-amino acid oxidase (DAAO). Various substituents were incorporated into kojic acid at its 2-hydroxymethyl group. These

Synthesis of tyrosinase inhibitory kojic acid derivative

Kojic acid derivative 2 was synthesized by joining two pyrone rings through an ethylene linkage by Horner-Emmons reaction of phosphonate 6 with aldehyde 7. The intermediates 6 and 7 were derived from kojic acid. The tyrosinase inhibitory activity of 2 was