Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Guanosine, 5 -phosphate, preparation

Enzyme preparations that can convert a-D-mannopyranosyl or 6-deoxy-a-D-Zt/xo-hexopyranosyl-4-ulose esters of guanosine 5 -pyro-phosphate into the /3-L-fucopyranosyl ester were obtained from Aerobacter aerogenes,99 432 Escherichia coli,100 Salmonella strains,433 higher plants,92 and animal tissues.434 Further purification of these enzymes will be necessary for mechanistic studies. [Pg.384]

Salts of the tetrafluoroaluminate (TFA) anion have been known for many years. Yet aqueous routes to pure materials have not been established despite the substantial amount of literature available on the subject. The present review will discuss the various synthetic methods that have been employed and will demonstrate a revised method for preparing pure TFA salts. These materials are important because TFA is able to stimulate various guanosine nucleotide-binding proteins (G-proteins) and inhibit P-type ATPases by serving as a nonhydrolyzing phosphate mimic. Additionally, various TFA salts serve as precursors to aluminum trifluoride, which is used as a catalyst for chlorofluorocarbon isomerizations and fluorinations. [Pg.181]

Chemical Synthesis.—Purine nucleoside 5 -monophosphates enriched with or 0 on the phosphate group are conveniently prepared by treating phosphorus pentachloride in dry triethyl phosphate with one equivalent of the appropriately labelled water to give PO]- or P 0]P0Cl3, which is not isolated but mixed with adenosine or guanosine in the same solvent. Work-up of the resulting 5 -phos-phorodichloridate in similarly labelled water permits the formation of pO]-or P 0]AMP (or GMP) in fair yield with good enrichment. The 5 -monophos-phates of the 5 -C-methyl uridines derived from 6-deoxy-D-allose and 6-deoxy-L-talose have been prepared via phosphorylation of the 2, 3 -0,0-ethoxymethyl-idene derivative of the nucleosides (1) with -cyanoethyl phosphate and DCC or TPS-Cl. The same method has been used to phosphorylate iV -benzoylated 2, 3 -0,C -isopropylidene derivatives of various 5 -C-alkyladenosine species (2) and also 4 -allyladenosine (3) as part of a study in which derivatives of AMP... [Pg.157]


See other pages where Guanosine, 5 -phosphate, preparation is mentioned: [Pg.131]    [Pg.355]    [Pg.60]    [Pg.92]    [Pg.155]    [Pg.28]    [Pg.238]    [Pg.339]    [Pg.343]    [Pg.118]    [Pg.120]    [Pg.210]    [Pg.305]    [Pg.135]    [Pg.118]    [Pg.120]    [Pg.52]    [Pg.55]    [Pg.185]    [Pg.137]    [Pg.170]    [Pg.66]    [Pg.54]    [Pg.180]    [Pg.185]    [Pg.423]    [Pg.591]    [Pg.149]    [Pg.577]    [Pg.156]    [Pg.134]    [Pg.268]    [Pg.360]    [Pg.208]    [Pg.220]    [Pg.229]    [Pg.185]    [Pg.162]    [Pg.166]    [Pg.183]    [Pg.268]    [Pg.220]    [Pg.78]    [Pg.150]   
See also in sourсe #XX -- [ Pg.54 ]




SEARCH



Guanosin

Guanosine

© 2024 chempedia.info