Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "aminoacyl adenylate analogues" wg kryterium: Temat


Wyświetlanie 1-1 z 1
Tytuł:
Bioaktywne N-acyloamidofosforanowe pochodne nukleozydów
Bioactive N-acylphosphoramidate nucleoside derivatives
Autorzy:
Kulik, K.
Powiązania:
https://bibliotekanauki.pl/articles/172366.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
ugrupowanie N-acyloamidofosforanowe
analogi aminoacyloadenylanów
analogi nukleozydów
Fosmidozyna
N-acylphosphoramidate function
aminoacyl adenylate analogues
nucleoside analogues
Phosmidosine
Opis:
Natural nucleotide antibiotics such as Agrocin 84, Dinoguellin, Microcin C and Phosmidosine have a N-acylphosphoramidate linkage at the 5’-hydroxyl of the adenosine derivatives (Fig. 1, 2) [1–3]. They exhibit interesting antifungal, antiemetics and anticancer properties. To synthesize these products, the construction of the N-acylphosphoramidate linkages seems to be a key step. Many groups have described the preparation of such a type of analogues but none of those methods was general. Grandas has for the first time reported the synthesis, of N-acylphosphoramidate peptide-oligonucleotide hybrids via condensation of N-phosphitylated carboxyamides with alcohols in the presence of 1H-tetrazole [9]. Based on this strategy Sekine synthesized aminoacyl adenylate (aa-AMP) analogues which could be useful in the studies on the recognition mechanism of the aminoacylation of tRNA and other biochemical reactions [10]. Since aa-AMPs are extremely unstable under aqueous conditions more stable analogues were required. Aminoacyl-adenylate analogues having an N-acylphosphoramidate linkage (aa-AMPN) could behave as potent, selective asparagine synthetase (AS) inhibitors because of its structural similarity to β-aspartyl-AMP (β AspAMP) which is natural product of AS [17]. Among natural N-acylphosphormiadates, Phosmidosine which connects a nucleoside analogue, 8-oxoadenosine, with an L-proline residue is unique because of its significant antitumor activities and property of stopping cell growth at the G1 phase in the cell cycle (Fig. 2) [2, 13]. The main difficulty during the synthesis of this compound is an extreme instability under weak basic conditions which excludes the use of labile protecting group of basic properties [14]. Stability studies have shown that under basic conditions phosphoryl group of Phosmidosine underwent rapid N–N migration (Scheme 9) [16]. Many modifications have been introduced to improve Phosmidosine properties [16]. Analogues such as demethylated species (Phosmidosine B) have proven to be stable under both basic and acid conditions and are also potential candidates for antitumor drugs [14].
Źródło:
Wiadomości Chemiczne; 2013, 67, 9-10; 877-897
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-1 z 1

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies