Pregled bibliografske jedinice broj: 1080365
Interactions of novel amidino-substituted aryl- bis(benzazoles) with DNA/RNA
Interactions of novel amidino-substituted aryl- bis(benzazoles) with DNA/RNA // Book of abstracts, 18th Ružička Days: Today science – tomorrow industry / Jukić, Ante (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2020. str. 46-46 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1080365 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Interactions of novel amidino-substituted aryl-
bis(benzazoles) with DNA/RNA
Autori
Ptiček, Lucija ; Racane, Livio ; Zonjić, Iva ; Tumir, Lidija-Marija ; Radić Stojković, Marijana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts, 18th Ružička Days: Today science – tomorrow industry
/ Jukić, Ante - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2020, 46-46
ISBN
978-953-6894-75-8
Skup
18. Ružičkini dani "Danas znanost - sutra industrija"
Mjesto i datum
Vukovar, Hrvatska, 16.09.2020. - 18.09.2020
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
amidines ; benzazoles ; interactions ; DNA/RNA
Sažetak
Series of eleven novel amidino-substituted bis(benzazoles), differing in heteroaromatic scaffolds as well as in type and position of amidine moiety, were studied for their binding abilities for DNA and RNA. By introducing different types of amidinic substituents and heteroaromatic substructure, namely benzothiazole, benzimidazole and benzoxazole, presented compounds were synthesized by condensation reaction of amidino-substituted 2- aminothiophenols, 2-aminophenols or o- phenylenediamines with isomeric aromatic dialdehydes or dicarboxylic acids by our previously developed method [1, 2]. Noncovalent binding interactions with DNA and RNA like intercalation, groove and electrostatic binding can be investigated by variety of methods. In order to detect possible presence of DNA/RNA active compounds in extracts, we utilized the most common methods in DNA binding studies: CD spectroscopy and the thermal denaturation of polynucleotides. While the former method monitors the impact of studied compounds on CD spectra of polynucleotides, the latter provides the information about the polynucleotide stabilization driven by compounds (ΔTm value). We used fluorimetry for the evaluation of the binding affinities. Competition dialysis experiment was used to probe the multitude of ligand-polynucleotide interactions. An array of different nucleic acid structures (single- stranded, double-stranded, DNA-RNA hybrid and triple helixes) were dialyzed against the compound solution for the assay. Dicationic compound 2-(2-(3-(6- carboximidamidiumbenzothiazole-2-yl)phenyl)- (benzothiazole-6-yl))-4, 5-dihydro-1H- imidazolium was identified as the most interesting one, as it showed high selectivity combined with high affinity over a particular polynucleotide structure. This compound was selected for detailed analysis with hybrid structure poly dA – poly rU by aforementioned methods.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
--IP-2018-01-4694 - Molekularno prepoznavanje DNA:RNA hibridnih i višelančanih struktura u bioanalitičkim i in vitro sustavima (DNARNAHyB-MolBio) (Radić Stojković, Marijana) ( CroRIS)
HRZZ-IP-2018-01-4379 - Istraživanje antioksidativnog djelovanja benzazolskog skeleta u dizajnu novih antitumorskih agensa (AntioxPot) (Hranjec, Marijana, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Tekstilno-tehnološki fakultet, Zagreb
Profili:
Marijana Radić Stojković (autor)
Lucija Ptiček (autor)
Iva Zonjić (autor)
Lidija-Marija Tumir (autor)
Livio Racane (autor)