Pregled bibliografske jedinice broj: 956106
Amino substituted benzamide derivatives as potential antioxidants
Amino substituted benzamide derivatives as potential antioxidants // 17. Ružičkini dani "Danas znanost – sutra industrija" : knjiga sažetaka = 17th Ružička days "Today science – tomorrow industry" : Book of Abstracts / Tomas, Srećko ; Ačkar, Đurđica (ur.).
Zagreb: Prehrambeno tehnološki fakultet Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2018. str. 27-27 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 956106 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Amino substituted benzamide derivatives as potential antioxidants
Autori
Perin, Nataša ; Hranjec, Marijana ; Roškarić, Petra ; Sović, Irena ; Boček, Ida ; Vianello, Robert ; Starčević, Kristina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
17. Ružičkini dani "Danas znanost – sutra industrija" : knjiga sažetaka = 17th Ružička days "Today science – tomorrow industry" : Book of Abstracts
/ Tomas, Srećko ; Ačkar, Đurđica - Zagreb : Prehrambeno tehnološki fakultet Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2018, 27-27
ISBN
978-953-6894-65-9
Skup
17. Ružičkini dani "Danas znanost - sutra industrija"
Mjesto i datum
Vukovar, Hrvatska, 19.09.2018. - 21.09.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
benzamide derivatives ; antioxidative potential ; computational study
Sažetak
In the last few decades, the search for the novel antioxidants led to the synthesis or isolation of different organic molecules which showed promising and more effective antioxidant activity in comparison with the standard antioxidants, such as vitamins C and A or BHT[1]. We prepared a range of N-arylbenzamides with a variable number of methoxy and hydroxy groups, bearing either amino or amino protonated moieties, and used DPPH and FRAP assays to evaluate their antioxidant capacity[2]. Most of the systems exhibit improved antioxidative properties relative to the reference BHT molecule in both assays. Combining results from both sets of experiments, the most promising antioxidative potential was displayed by the trihydroxy derivative, which we propose as a lead compound for a further optimization of the benzamide scaffold. Computational analysis helped in interpreting the observed trends and demonstrated that protonated systems are better antioxidants than their neutral counterparts, while underlying the positive influence of the electron-donating methoxy group on the antioxidant properties, thus confirming the experiments. It also revealed that the introduction of the hydroxy groups shifts the reactivity from both amide and amine groups towards this moiety and additionally enhances antioxidative features.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-3386 - Dizajn i sinteza novih dušikovih heterocikličkih fluorofora i fluorescentnih nanomaterijala kao kemijskih senzora za pH i metalne ione (iNFiNiTE–SENS) (Vianello, Robert, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Veterinarski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Kristina Starčević
(autor)
Robert Vianello
(autor)
Irena Sović
(autor)
Ida Boček Pavlinac
(autor)
Petra Roškarić
(autor)
Marijana Hranjec
(autor)
Nataša Perin
(autor)