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Antibiotiki ; 23(1): 26-30, 1978 Jan.
Article in Russian | MEDLINE | ID: mdl-623445

ABSTRACT

A non-reducing disugar and amino acid were isolated in the studies on the structure of parvulomycin. The acid hydrolysis of the disugar revealed the presence of 2 moles of D-glucose. Acetylation of the disugar resulted in formation of octa-O-acetyl-alpha,alpha-tregalose, saponification of which resulted in formation of alpha,alpha-tregalose. Its physical parameters, i.e. melting point of the mixed sample, optical rotation, IR-spectrum coincided with those of the authentic alpha,alpha-tregalose. The isolated amino acid proved to be L-glutamic acid on thin-layer chromatography with witness and comparison of the physico-chemical properties of their hydrochlorides.


Subject(s)
Antifungal Agents/analysis , Disaccharides/isolation & purification , Glutamates/isolation & purification , Trehalose/isolation & purification , Acetylation , Amino Acids/analysis , Aminoglycosides , Chromatography , Chromatography, Paper , Glycosides/analysis , Hydrolysis , Magnetic Resonance Spectroscopy , Methylation , Molecular Conformation
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