69882-69-5

Upstream product

• 28030-16-2 3-(4-methoxyphenyl)-2-oxopropanoic acid 
• 69274-58-4 2,2-Dimethoxy-3-(4-methoxy-phenyl)-propionic acid methyl ester 
• 41339-41-7 ethyl 3-cyano-3-(p-methoxyphenyl)-pyruvate 
• 68383-86-8 2-hydroxy-3-(4-methoxyphenyl)acrylic acid 
• 74-88-4 methyl iodide 
• 4410-99-5 2-mercaptophenylethane 
• 96125-49-4 methyl trans-3-(4-methoxyphenyl)glycidate 

Downstream Products

• 858216-86-1 4-(4-methoxy-phenyl)-5-phenyl-dihydro-furan-2,3-dione 
• 100474-32-6 3-[4-Hydroxy-3-(4-methoxy-phenyl)-5-oxo-2,5-dihydro-furan-2-yl]-propionic acid ethyl ester 
• 473401-85-3 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 86603-45-4 methyl 3-bromo-3-(4-methoxyphenyl)pyruvate 
• 100474-78-0 3-[4-Hydroxy-3-(4-methoxy-phenyl)-5-oxo-2,5-dihydro-furan-2-yl]-propionic acid 
• 142011-36-7 2-<(4-methoxyphenyl)methyl>-2-thiazolidinecarboxylic acid methyl ester 
• 170238-94-5 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Synthesis and biological evaluation of analogues of butyrolactone I and molecular model of its interaction with CDK2.

A series of analogues of butyrolactone I, a natural product isolated from Aspergillus terreus that selectively inhibits the CDK2 and CDK1 kinases and that has been found to exhibit an interesting antiproliferative activity, have been synthesized. Its anti