Biosynthesis of alkaloids in Sophora alopecuroides

Autor:	S. Kuchkarov, Kh. A. Aslanov, Kh. R. Sohütte, Yu. K. Kushmuradov
Rok vydání:	1977
Předmět:	Stereochemistry Alkaloid Sparteine Reverse transition Pachycarpine Plant Science General Chemistry General Biochemistry Genetics and Molecular Biology chemistry.chemical_compound Cytisine Biosynthesis chemistry medicine Sophora alopecuroides Allomatrine medicine.drug
Zdroj:	Chemistry of Natural Compounds. 13:207-210
ISSN:	1573-8388 0009-3130
DOI:	10.1007/bf00563949
Popis:	The interconversions of the alkaloids of Sophora alopecuroides L. have been studied by feeding the plants with tritium-labelled alkaloids ([3H]sophoridine, [3H]pachycarpine, [3H]cytisine, [3H]isosophoridine, [3H]allomatrine, and [3H]N-methylcytisine). It has been established that the conformationally stable isomers of the alkaloids — isosophoridine and allomatrine — do not take part actively in the metabolism of the alkaloids. It has also been shown that the alkaloids of the sparteine group are converted into martrine alkaloids in the development of the plant. The methylation of cytisine to N-methylcytisine and the reverse transition have been shown experimentally in the plant organism.
Databáze:	OpenAIRE
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