Pregled bibliografske jedinice broj: 21690
Synthesis and Spectroscopic Evidences of Aminoacid Esters of 4',5'-Isobutyliden-O-protected Pyridoxine
Synthesis and Spectroscopic Evidences of Aminoacid Esters of 4',5'-Isobutyliden-O-protected Pyridoxine // European Journal of Pharmaceutical Sciences-Abstracts of Fourth European Congress of Pharmaceutical Sciences / Junginger, Hans E. ; Mulder, Gerard J. (ur.).
Amsterdam: Elsevier, 1998. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 21690 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and Spectroscopic Evidences of Aminoacid Esters of 4',5'-Isobutyliden-O-protected Pyridoxine
Autori
Jadrijević-Mladar Takač, Milena ; Vuković, Jadranka ; Vikić-Topić, Dražen
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Journal of Pharmaceutical Sciences-Abstracts of Fourth European Congress of Pharmaceutical Sciences
/ Junginger, Hans E. ; Mulder, Gerard J. - Amsterdam : Elsevier, 1998
Skup
Fourth European Congress of Pharmaceutica Science
Mjesto i datum
Milano, Italija, 11.09.1998. - 13.09.1998
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Amino acid esters; B6 vitamin; isobutylidenpyridoxine; 1D and 2D NMR; 1H and 13 C NMR spectroscopy
(Amino acid esters; B6 vitamin; isobutylidenpyridoxine; 1D and 2D NMR; 1H and 13C NMR spectroscopy)
Sažetak
The preparation of ?-aminoacid esters with pyridoxine (B6 vitamin) were investigated. The scope of investigation was the synthesis of the potential "pro drug" substances for the therapy of metabolic disorders that required an increased input of the corresponding essential ?-aminoacid (i.e., cirrhosis, hepatic encephalophaty, liver and renal failure). For this purpose both ?-aminoacid esters from BOC- and Z-N-protected aminoacids (Gly-OH, Ala-OH, Leu-OH and Phe-OH) and 4', 5'- isobutyliden pyridoxine with addition of DCC were synthesized. Chemical structures of obtained esters were determined by IR, one- and two-dimensional, homo- and heteronuclear 1H and 13C NMR correlation spectra (COSY, NOESY, HETCOR and HMBC). BOC-N-protected aminoacids gave better yields in comparing to Z-aminoacids, and the most reactive was BOC-Phe-OH. The use of unprotected pyridoxine, as an alcoholic component, in the same reaction condition with excess of amino acid and DCC (pyridoxine:aminoacid:DCC=1:3:3), gave a mixture of mono-, di- and tri-esters. The removing of protecting group by trifluoroacetic acid, from aminoacid's part of ester, gave and other products of reaction, so the selective removings of protecting group remain for the further investigation.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb
Profili:
Jadranka Vuković Rodriguez
(autor)
Milena Jadrijević-Mladar Takač
(autor)
Dražen Vikić-Topić
(autor)