Pregled bibliografske jedinice broj: 86061
Synthesis And Biological Evaluation Of Fluorinated And Iodinated Purine Acyclic Nucleoside Analogues
Synthesis And Biological Evaluation Of Fluorinated And Iodinated Purine Acyclic Nucleoside Analogues // XV International Round Table "Nucleosides, Nucleotides & Nucleic Acids" : abstracts ; P-79 / De Clercq, Erik, Herdewijn, Piet (ur.).
Leuven, 2002. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 86061 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis And Biological Evaluation Of Fluorinated And Iodinated Purine Acyclic Nucleoside Analogues
Autori
Prekupec, Svjetlana ; Gazivoda, Tatjana ; Raić-Malić, Silvana ; Balzarini, Jan ; De Clercq, Erik ; Mintas, Mladen
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
XV International Round Table "Nucleosides, Nucleotides & Nucleic Acids" : abstracts ; P-79
/ De Clercq, Erik, Herdewijn, Piet - Leuven, 2002
Skup
International Round Table "Nucleosides, Nucleotides & Nucleic Acids" (15 ; 2002)
Mjesto i datum
Leuven, Belgija, 10.09.2002. - 14.09.2002
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Sažetak
Gene therapy (suicide gene therapy) is a method which uses herpes simplex virus thymidine kinase (HSV-1 TK) and prodrug (ganciclovir-GCV) combination for the treatment of cancer. That approach has been succesfully applied for the treatment of bone marrow transplantation and for patients who developed lymphomas. However, one of the limitations of this method is ganciclovir resistance to cytomegalovirus infections that frequently occur in allo-BMT patients. The main goal of this study is to synthesize the new acyclic nucleosides as prodrugs which could find a succesful application in gene therapy of cancer. It was found that acyclic nucleoside analogues with 9-(2-hydroxypropyl) and 9-(2-hydroxyetoxymethyl) side chain act as fraudulent substrates for HSV-1 TK. Therefore, the new acyclic nucleoside derivatives (A and B) were synthesized. The novel compounds were evaluated against: murine leukemia (L1210/0), murine mammary carcinoma (FM3A) and human T-lymphocytes (Molt4/C8 and CEM/0). Acetylated acyclic nucleosides containing iodine and chlorine in the positions 2 and 6, respectively, exhibit marked inhibitory effects against malignant tumor cell lines: L1210/0, Molt4/C8 and CEM/0. [1] P. Pospisil, B. D. Pilger, P. Schelling, C. Wurth, L. Scapozza, G. Folkers, M. Pongracic, M. Mintas and S. Raic-Malic, Helv. Chim. Acta, submitted.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
0125003
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Mladen Mintas
(autor)
Svjetlana Krištafor
(autor)
Silvana Raić-Malić
(autor)
Tatjana Gazivoda Kraljević
(autor)