Pregled bibliografske jedinice broj: 478562
Synthesis, photochemical synthesis and antitumor evaluation in vitro of novel derivatives of benzothieno and thienothieno quinolones
Synthesis, photochemical synthesis and antitumor evaluation in vitro of novel derivatives of benzothieno and thienothieno quinolones // IUPAC ICOS-18 / Hans-Rene Bjorsvik (ur.).
Bergen: Allkopi, 2010. str. 102-442 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 478562 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis, photochemical synthesis and antitumor evaluation in vitro of novel derivatives of benzothieno and thienothieno quinolones
Autori
Aleksić, Maja ; Uzelac, Lidija ; Kralj, Marijeta ; Karminski-Zamola, Grace
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
IUPAC ICOS-18
/ Hans-Rene Bjorsvik - Bergen : Allkopi, 2010, 102-442
ISBN
978-82-992954-5-8
Skup
The 18 International Conference of Organic Synthesis
Mjesto i datum
Bergen, Norveška, 01.08.2010. - 06.08.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Synthesis; photochemical synthesis and antitumor evaluation in vitro; benzothieno and thienothieno quinolones
Sažetak
Heterocyclic amides and their cyclic derivatives, quinolones, are structural part of a large number of natural compounds. Due to the wide range of biological activities, they are the subject of intense research of synthetic organic and medicinal chemists with the aim of finding selective therapeutic agents.1 Previously prepared derivatives of benzo[b]thieno-, thieno[2', 3':4, 5]thieno- and thieno[3', 2':4, 5]thieno[2, 3-c]quinolones showed very good antitumor activity in vitro on a number of human tumor cell lines. Some of these compounds efficiently bind to double- stranded polynucleotides by intercalation.2, 3 Searching for compounds related to these classes of biologically and pharmacologically active compounds, new derivatives of benzo[b]thiophene, thieno[2, 3-b]thiophene and thieno[3, 2-b]thiophene carboxamides were prepared in a multistep synthesis.4 Their cyclic analoges were prepared by photochemical dehydrohalogenation. All compounds were characterized by 1H, 13C NMR, IR and UV/Vis spectroscopy. Antitumor activity in vitro was tested on 5 human tumor cell lines. Based on in vitro screening results all compounds showed high antiproliferative effect.
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:
Lidija Uzelac
(autor)
Grace Karminski-Zamola
(autor)
Marijeta Kralj
(autor)
Maja Cindrić
(autor)