“…It was found that only compounds 4 and 6 with phenolic groups demonstrated a radical scavenging activity (Table 2), which indicated that these compounds act mainly through the HAT mechanism; for compound 6 the IC 50 value was 20.09 ± 0.02 µM [29]. The obtained data were consistent with the literature data, according to which sterically hindered phenols are good antioxidants due to their ability to form stable aroxyl radicals [30].…”
Section: Reducing Activity Of Compoundssupporting
confidence: 87%
“…The addition of diphenyltrisulfide 1 to the liver homogenate reduced the level of TBARS after 1 h of incubation by 64%, but the efficiency of the antioxidant action decreased after 24 h to 48%, and after 48 h to 37% without inversion of properties. In the previous research, we found that bis(3,5-di-tert-butyl-4-hydroxyphenyl) disulfide 6 exhibited a pronounced antioxidant effect at all stages of LPO, and diphenyl disulfide 5 had a prolonged prooxidant activity [29]. It was previously shown that the rate of interaction of polysulfides with peroxides was proportional to the number of sulfur atoms in the polysulfide structure [54].…”
Section: Determination Of the Accumulation Level For Tbars In The Liv...mentioning
confidence: 92%
“…The studied disulfides 4 (TCI, 98%) and 5 (Sigma Aldrich, Burlington, MA, USA, 99%) are commercially available compounds. Disulfide 6 was synthesized according to the previously described method with slight modifications [29,69].…”
Section: General Procedures and Synthesesmentioning