A Structure–Activity Relationship Study on the Antioxidant Properties of Dithiocarbamic Flavanones

• DOI: 10.3390/antiox13080963
• Publication Date: 2024-08-09T13:48:54Z
• Authors: Mihail Lucian Birsa; Laura Gabriela Sarbu
• Keywords: Butylated hydroxytoluene; Moiety; ABTS; Flavanone

The antioxidant properties of 3-dithiocarbamic flavanones have been investigated. influence the halogen substituents on ring A and nature secondary amine from dithiocarbamic moiety accounted. results indicated that presence a substituent at C-8 position benzopyran induce better against DPPH ABTS than butylated hydroxytoluene (BHT) ascorbic acid. mentioned appears to higher stability for free radical intermediate C-3 ring. enolate is most likely be involved in activity this flavanone. It stable supports reported flavanones.