Pregled bibliografske jedinice broj: 1011823
Time-dependent cytotoxicity of pyridinium antidotes
Time-dependent cytotoxicity of pyridinium antidotes // Final Programme of the 44th FEBS Congress and Book of Abstract at the 19th YSF FEBS 2019, Krakow, Poland
Kraków, Poljska, 2019. str. 46-46 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1011823 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Time-dependent cytotoxicity of pyridinium antidotes
Autori
Zandona, Antonio ; Madunić Josip ; Katalinić, Maja
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Final Programme of the 44th FEBS Congress and Book of Abstract at the 19th YSF FEBS 2019, Krakow, Poland
/ - , 2019, 46-46
Skup
44th FEBS Congress and the 19th FEBS Young Scientists' Forum
Mjesto i datum
Kraków, Poljska, 03.07.2019. - 11.07.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
time-dependent, cytotoxicity, oximes, pyridinium, antidotes
Sažetak
The better selection of a lead candidate for preclinical drug development has come into strong demand in recent years. In that sense, early, rapid and robust results, that unambiguously rank compounds for their desirable and undesirable effects, put cell- based in vitro toxicology in major focus. In the preclinical selection of the most efficient antidotes for organophosphorus pesticide and nerve warfare agents poisoning, we evaluated the time-dependent cytotoxicity of the leading oxime compounds. We evaluated a structurally dependent series of oximes bearing up to two chlorine atoms that showed a promising antidote potential in the previous studies. The cytotoxic effect was evaluated on several cell lines in a wide oxime concentration range and at least three time points. The results were compared to the oxime HI-6, which is used today as an antidote in medical practice. As results indicate, time-dependent toxicity of tested oximes was strongly related to their structure and the ones having both a but-2(E)-en-1, 4-diyl linker and chlorine atoms were the most toxic to all cells tested. The IC50 determined by the MTS assay was in the μM range. This effect was also confirmed by additionally testing the ATP status of the cells. Though the mechanism behind this toxicity needs to be confirmed, such a result indicates that these oximes have limitations if considered for further antidote development. Acknowledgment: This work was supported in part by the Croatian Science Foundation under the project UIP-2017-05-7260.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
HRZZ-UIP-2017-05-7260 - MOLEKULARNI MEHANIZMI TOKSIČNOSTI PROTUOTROVA I POTENCIJALNIH LIJEKOVA (CellToxTargets) (Katalinić, Maja, HRZZ - 2017-05) ( CroRIS)
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb