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Bioorg Khim ; 13(5): 648-53, 1987 May.
Article in Russian | MEDLINE | ID: mdl-3040014

ABSTRACT

Phosphonate analogues of 2-N-stearoyl- (I) and 2-N-(undec-10-enoyl)-sphingomyelins (II) have been synthesised. Compound (II) was used as a starting product for preparation of a sorbent for sphingomyelinase affinity chromatography. The double bond of the unsaturated undec-10-enoyl moiety of the phosphonate analogue (II) was oxidized, and the modified (II) was coupled to amino-Toyopearl HW-65 to give a sorbent containing 4 mumoles of ligand per milliliter of the swollen resin.


Subject(s)
Organophosphorus Compounds/chemical synthesis , Phosphoric Diester Hydrolases/isolation & purification , Sphingomyelin Phosphodiesterase/isolation & purification , Sphingomyelins/chemical synthesis , Bacillus cereus/enzymology , Chemical Phenomena , Chemistry , Chromatography, Affinity , Ligands
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