Pregled bibliografske jedinice broj: 1032095
Quinone Methide Precursors with BODIPY Chromophore: Synthesis, Photochemistry and Biological Activity
Quinone Methide Precursors with BODIPY Chromophore: Synthesis, Photochemistry and Biological Activity // 3rd mini symposium of medicinal and pharmaceutical section / Fidelta d.o.o., Zagreb
Zagreb, Hrvatska, 2019. str. 8-8 (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1032095 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Quinone Methide Precursors with BODIPY Chromophore: Synthesis, Photochemistry and Biological Activity
Autori
Zlatić, Katarina ; Uzelac, Lidija ; Kralj, Marijeta ; Basarić, Nikola
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
3rd mini symposium of medicinal and pharmaceutical section / Fidelta d.o.o., Zagreb
/ - , 2019, 8-8
Skup
3rd mini symposium of medicinal and pharmaceutical section
Mjesto i datum
Zagreb, Hrvatska, 12.11.2019
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
photochemistry ; quinone methide ; BODIPY
Sažetak
Quinone methides (QM) are reactive intermediers that can be generated in photochemical reactions, such as photodeamination.1-4 QMs exhibit biological activity, which is related to their ability to react in Michael addition reactions with various amines and sulfides, including amino acids and nucleotides.5-6 Reaction with nucleotides induce DNA alkylation and cross-linking, and consequently, cytotoxicity.7-9 Photochemical generation of QMs under mild conditions and citotoxic biological activity make QM precursor molecules potential photoactivable anticancer drugs. We incorporated QM precursor units into BODIPY chromophore to obtain molecules with desired photochemical properties which can be excited by visible light.10 BODIPY derivates are commonly used as dyes for biomolecular labeling since they are characterized by good photochemical stability and excellent photophysical and spectral properties.11 Several BODIPY-QM precursor molecules have been synthesized and their photophisical properties and photochemical reactivity were investigated. The experimental observations were backed up by TD-DFT calculations. Non-covalent interactions of BODIPY-QM precursors with biomacromolecules and the ability of photochemically formed QMs to alkylate biomacromolecules were demonstrated by photonduced fluorescent labeling of bovine serum albumin.12 Furthermore, antiproliferative activity of synthesized BODIPY-QM precursors was investigated using MTT assay on several human cancer cell lines with and without irradiation.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
HRZZ-IP-2013-11-5660 - Mulitidisciplinarni pristup otkriću lijekova s ciljanim djelovanjem na matične stanice tumora – uloga transporta kalija (MultiCaST) (Kralj, Marijeta, HRZZ - 2013-11) ( CroRIS)
HRZZ-IP-2014-09-6312 - Supramolekulska kontrola fotokemijskih reakcija eliminacije (SupraPhotoE) (Basarić, Nikola, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Lidija Uzelac
(autor)
Marijeta Kralj
(autor)
Katarina Zlatić
(autor)
Nikola Basarić
(autor)