k 2019

New 1 3 5-triazine Derivatives Incorporating Aminobenzenesulfonamide, Aminoalcohol, Piperazine, Chalcone or Stilbene Structural Motifs and Evaluation of Their Antioxidative Activity (PDF) New 1,3,5-triazine Derivatives Incorporating Aminobenzenesulfonamide, Aminoalcohol, Piperazine, Chalcone or Stilbene Structural Motifs and Evaluation of Their Antioxidative Activity. Available from: https://www.researchgate.net/publication/337285387_New_135-triazine_Derivatives_Incorporating_Aminobenzenesulfonamide_Aminoalcohol_Piperazine_Chalcone_or_Stilbene_Structural_Motifs_and_Evaluation_of_Their_Antiox

HAVRÁNKOVÁ, Eva; Nikola ČALKOVSKÁ; Tereza PADRTOVÁ; Jozef CSÖLLEI; Radka OPATŘILOVÁ et al.

Základní údaje

Originální název

New 1 3 5-triazine Derivatives Incorporating Aminobenzenesulfonamide, Aminoalcohol, Piperazine, Chalcone or Stilbene Structural Motifs and Evaluation of Their Antioxidative Activity (PDF) New 1,3,5-triazine Derivatives Incorporating Aminobenzenesulfonamide, Aminoalcohol, Piperazine, Chalcone or Stilbene Structural Motifs and Evaluation of Their Antioxidative Activity. Available from: https://www.researchgate.net/publication/337285387_New_135-triazine_Derivatives_Incorporating_Aminobenzenesulfonamide_Aminoalcohol_Piperazine_Chalcone_or_Stilbene_Structural_Motifs_and_Evaluation_of_Their_Antiox

Autoři

HAVRÁNKOVÁ, Eva ORCID; Nikola ČALKOVSKÁ; Tereza PADRTOVÁ; Jozef CSÖLLEI; Radka OPATŘILOVÁ a Pavel PAZDERA

Vydání

The 23rd International Electronic Conference on Synthetic Organic Chemistry, 2019

Další údaje

Jazyk

angličtina

Typ výsledku

Prezentace na konferencích

Obor

10401 Organic chemistry

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Označené pro přenos do RIV

Ne

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

1 3 5-triazine; 4-aminophenol; hydroxychalcone; hydroxystilbene; antioxidative activity; ABTS method
Změněno: 23. 2. 2021 12:20, Mgr. Hana Hurtová

Anotace

V originále

A series of 1,3,5-triazine derivatives, incorporating aminobenzenesulfonamide, aminoalcohol/phenol, piperazine, chalcone, or stilbene structural motifs, were evaluated as potential antioxidants. The compounds were prepared by using step by step nucleophilic substitution of chlorine atoms in starting 2,4,6-trichloro-1,3,5-triazine. Reactions were catalyzed by Cu(I)-supported on a weakly acidic resin. The radical scavenging activity was determined in terms of %inhibition activity and IC50, using the ABTS method. Trolox and ascorbic acid (ASA) were used as standards. In the lowest used concentration 1 × 10-4 M, the %inhibition activity at time 0 min was comparable with both standards at least for 10 compounds. After 60 min compounds 1, 2, 9 and 25 showed nearly twice %inhibition (73.44–87.09%) in comparison with standards (Trolox = 41.49%; ASA = 31.07%). Values of IC50 correlated with %inhibition activity. For compounds 1, 2, 9 and 25 values of IC50 in time 60 min (17.16–27.78 μM) were 5 times lower than IC50 of both standards (Trolox = 178.33 μM; ASA = 147.47 μM). Based on these results, the presented 1,3,5-triazine derivatives and their analogs have a high potential in the treatment of illnesses caused or related to oxidative stress.