Pregled bibliografske jedinice broj: 296310
New Acyclic Purine Nucleoside Analoques Containing Exocyclic Pyrrolo Moiety: Synthetic and X-Ray Crystal Structure Study
New Acyclic Purine Nucleoside Analoques Containing Exocyclic Pyrrolo Moiety: Synthetic and X-Ray Crystal Structure Study // The tenth Dubrovnik International Course and Conference on the Interfaces among Mathematics, Chemistry and Computer Sciences : abstracts
Dubrovnik, Hrvatska, 1995. (poster, nije recenziran, neobjavljeni rad, znanstveni)
CROSBI ID: 296310 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
New Acyclic Purine Nucleoside Analoques Containing Exocyclic Pyrrolo Moiety: Synthetic and X-Ray Crystal Structure Study
Autori
Raić, Silvana ; Pongračić, Mario ; Vorkapić-Furač, Jasna ; Hergold-Brundić, Antonija ; Nagl, Ante ; Mintas, Mladen
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, neobjavljeni rad, znanstveni
Izvornik
The tenth Dubrovnik International Course and Conference on the Interfaces among Mathematics, Chemistry and Computer Sciences : abstracts
/ - , 1995
Skup
Dubrovnik International Course and Conference on the Interfaces among Mathematics, Chemistry and Computer Sciences
Mjesto i datum
Dubrovnik, Hrvatska, 26.06.1995. - 01.07.1995
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
aciklički purinski nukleozidni analozi ;
(acyclic purine nucleoside analogues ; potential antiviral agents)
Sažetak
There has been considerable interest in nucleosites modified on the sugar moiety as potential antiviral agents. The search for new antiviral drugs led to the synthesis of a large number of acyclic nucleosides. Furthermore, adenine analofues have been used as plant growth factors (cytokinines) important for plant cell division and differentiation. In the search of molecules related to those classes of biologically and pharmacologically active compounds and in continuation to our previous research in this field, we have prepared the novel 6-(N-pyrroly) purine nucleoside analogues l -7 with acyclic side chains attached to the N-9 position of the purine ring. The site of alkylation of the purine ring was deduced on the basis of their lH and 13C NMR spectra. The conformation of the dimeric structure 6 was determined by its X-ray crystalographic analysis.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Mladen Mintas
(autor)
Mario Pongračić
(autor)
Silvana Raić-Malić
(autor)
Antonija Hergold-Brundić
(autor)
Jasna Vorkapić-Furač
(autor)