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Pregled bibliografske jedinice broj: 884230

Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding


Husak, Antonija; Matić, Josipa; Piantanida, Ivo; Basarić, Nikola
Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding // 10th Joint Meeting of Medicinal Chemistry / Dubrovnik, Hrvatska
Dubrovnik, Hrvatska, 2017. str. 121-121 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding

Autori
Husak, Antonija ; Matić, Josipa ; Piantanida, Ivo ; Basarić, Nikola

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
10th Joint Meeting of Medicinal Chemistry / Dubrovnik, Hrvatska / - , 2017, 121-121

ISBN
978-953-55232-8-4

Skup
10th Joint Meeting of Medicinal Chemistry / Dubrovnik, Hrvatska

Mjesto i datum
Dubrovnik, Hrvatska, 25-28.06. 2017

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Quinone methides, peptides, DNA

Sažetak
Quinone methides (QMs) are recative intermediates with a potential in the development of new leads for drugs owing to their reactivity with DNA, proteins and enzymes [1]. In particular, some anticancer antibiotics such as mitomycine base their action on metabolic formation of QMs and subsequent DNA cross-linking. Therefore, it is important to investigate different classes of simple QMs as potential anticancer agents. However, QM are reactive intermediates with short inherent lifetimes, so they have to be prepared in situ in the living cells. An excellent methodology for the generation of QMs in the biological systems are photochemical reactions of deamination or dehydration [2]. We have recently demonstrated that tyrosine derivatives can be modified into QM precursors and imbedded in proteins where they remain photochemically reactive [3]. Furthermore, it is known that photo-triggered DNA alkylation by QMs can be significantly enhanced by binding QM precursors to the DNA intercallators [4]. Here we present synthesis of dipeptides 1 and 2 that contain two unnatural amino acids, photochemically reactive tyrosine derivative and aminoacid bearing DNA intercalators- phenantridine [5] or pyrene [6]. Their non-colvalent and photo-triggered covalent DNA binding ability will be investigated.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2013-11-1477 - Višenamjensko očitavanje DNA / RNA sekundarne strukture molekularnim kemijskim senzorima (Ivo Piantanida, )
HRZZ-IP-2014-09-6312 - Supramolekulska kontrola fotokemijskih reakcija eliminacije (Nikola Basarić, )

Ustanove
Institut "Ruđer Bošković", Zagreb