Glucoside. I
نویسندگان
چکیده
منابع مشابه
Properties of pyridoxine glucoside.
Intact pyridoxine glucoside showed about 20% of microbiological activity of equivalent mole of pyridoxine for Saccharomyces carlsbergensis 4228 ATCC 9080. The activity was gradually increased accompanied with the prolonged incubation. It seems that pyridoxine glucoside is hydrolyzed to pyridoxine and glucose by a-glucosidase of Saccharomyces carlsbergensis 4228 ATCC 9080 and can be bioassayed a...
متن کاملStudies on the alpha-glucoside hydrolase inhibitor, adiposin. I. Isolation and physicochemical properties.
In the case of metabolic disorders such as diabetes, hyperglycemia, or hyperlipemia, it is well known that the blood levels of glucose, insulin, and lipoprotein, especially after food intake, differ from the normal levels. One of the reasonable countermeasures to these carbohydrate dependent diseases will be to limit intestinal carbohydrate digestion by the administration of a-glucoside hydrola...
متن کاملHYDROLYSIS OF SUCROSE BY INVERTASE IN THE PRESENCE OF (r-METHYL GLUCOSIDE. I.*
It has been observed by Michaelis and Pechstein (1) and others, that a-methyl glucoside manifests a marked retarding influence on the hydrolysis of sucrose by invertase. The curves given in Fig. 1 represent the hydrolysis of a 10 per cent sucrose solution by invertase in the presence and absence of the glucoside. Nelson and Hitchcock (2) found that the hydrolysis of 10 per cent sucrose solution...
متن کاملStudies of mammalian glucoside conjugation.
The mammalian glucoside-conjugation pathway was studied by using p-nitrophenol as the model substrate and mouse liver microsomal preparations as the source of enzyme. The microsomal preparations supplemented with UDP-glucose glucosylated p-nitrophenol; p-nitrophenyl glucoside was identified by chromatography in six solvent systems. The unsolubilized glucosyltransferase of fresh microsomal prepa...
متن کاملThiazolylmethyl ortho-substituted phenyl glucoside library as novel C-aryl glucoside SGLT2 inhibitors.
In order to investigate SAR regarding proximal phenyl ring in novel C-aryl glucoside SGLT2 inhibitors containing a thiazole motif, a series of chemical modifications on proximal phenyl ring was conducted. During a series of lead optimization efforts, ortho-allyloxyphenyl 10p or ortho-hydroxyphenyl 11a showed subnanomolar inhibitory activity against hSGLT2.
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ژورنال
عنوان ژورنال: NIPPON KAGAKU KAISHI
سال: 1930
ISSN: 0369-4208,2185-0909
DOI: 10.1246/nikkashi1921.51.357