Pregled bibliografske jedinice broj: 478556
Synthesis, antitumor activity in vitro and interaction with ct-DNA of novel benzimidazo[1, 2-a]quinoline derivatives
Synthesis, antitumor activity in vitro and interaction with ct-DNA of novel benzimidazo[1, 2-a]quinoline derivatives // IUPAC ICOS-18, The 18th International Conference on Organic Synthesis, August 1-6, 2010, Bergen, Norveška / Hans-Rene Bjorsvik (ur.).
Bergen: Allkopi, 2010. str. 063-457 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 478556 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis, antitumor activity in vitro and interaction with ct-DNA of novel benzimidazo[1, 2-a]quinoline derivatives
Autori
Perin, Nataša ; Hranjec, Marijana ; Marjanović, Marko ; Kralj, Marijeta ; Karminski-Zamola, Grace
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
IUPAC ICOS-18, The 18th International Conference on Organic Synthesis, August 1-6, 2010, Bergen, Norveška
/ Hans-Rene Bjorsvik - Bergen : Allkopi, 2010, 063-457
ISBN
978-82-992954-5-8
Skup
18th International Conference on Organic Synthesis
Mjesto i datum
Bergen, Norveška, 01.08.2010. - 06.08.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Synthesis; antitumor activity in vitro and interaction with ct-DNA of novel benzimidazo[1; 2-a]quinoline derivatives
Sažetak
One of the most important goals in medicinal chemistry is the development of new heterocyclic compounds with antitumor activity. Since the benzimidazole unit is the key building block for a variety of compounds which have crucial roles in the functions of biologically important molecules, there is a constant and growing interest over the past few years for the synthesis and biological studies of benzimidazole derivatives.1, 2 As a part of our continuing research in the field of medicinal chemistry, novel nitro- and amino substituted benzimidazole and benzimidazo[1, 2- a]quinoline derivatives as a potential biologically active agents were synthesized. For the preparation of targeted compounds, clasicall reactions of organic chemistry and photochemistry were used. All compounds were characterized by 1H, 13C NMR, IR, UV/Vis and fluorimetric spectroscopy. Preliminary interaction of amino-benzimidazo[1, 2- a]quinolines 5 and 8 with ct-DNA was studied by UV/Vis and fluorimetric spectroscopy and from obtained results we can conclude that this compounds showed strong interaction with ct- DNA. One of examinated compound showed increase of fluorescence intensity during the titration with ct-DNA and thus have possible application as fluorescent probe for nucleic acid detection in biomedicine. Antitumor activity in vitro of prepared compounds was tested on several human tumour cell lines.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
098-0982464-2514 - Uloga različitih mehanizama odgovora stanica na terapiju oštećenjem DNA (Kralj, Marijeta, MZOS ) ( CroRIS)
125-0982464-1356 - Novi heterocikli kao antitumorski i antivirusni (pametni) lijekovi (Hranjec, Marijana, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Marko Marjanović
(autor)
Grace Karminski-Zamola
(autor)
Marijeta Kralj
(autor)
Nataša Perin
(autor)
Marijana Hranjec
(autor)