Article: Reports from P. Bandyopadhyay et al highlight recent research in agricultural and food chemistry.

According to recent research published in the Journal of Agricultural and Food Chemistry, "Several novel picolyl alkyl amine derivatives (A-L) were synthesized, and the influence of hydrophobicity and substitution on the inhibition of mushroom tyrosinase toward both monophenolase and diphenolase activities are described. alpha-, beta-, and gamma-picolyl amines are neither the substrates nor the inhibitors; however, the inhibition is induced by the incorporation of an alkyl chain."

"The inhibition was strongly dependent on the substitution on a pyridine ring, and the inhibition follows the trend of alpha-picolyl alkyl amines (A, D, G)

The researchers concluded: ...

Related newspaper, magazine, and journal articles:

 
 
Newsweek Harper's Magazine The Washington Post Chicago Tribune Crain's Chicago Business PRNewswire Pediatric News The Nation Advertising Age The Economist (US) A FREE trial gives you access to over 80 million articles! Access over 6,500 publications with a FREE trial!