Abstract

Accrding to the procedure of Osipow, sucrose was partially acylated with palmitic, stearic, hydnocarpic, and ricinoleic acids. In the similar manner, the selective esterification of trehalose was performed, using caprylic, lauric, myristic, and stearic acids. The ester compositions of the resulting preparations were preliminarilly analysed by means of thin-layer chromatography and gas chromatography, and the major components contained in them were tentatively assigned to the 6-monoesters of these disaccharides. All the preparations obtained proved to exert considerable antitumor effect against Ehrlich ascites carcinoma in mice by intraperitoneal administration.

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