The chemotaxonomic significance of laricytrin and medicagenic acid in the tribe Trigonelleae

1988 ◽  
Vol 66 (2) ◽  
pp. 363-367 ◽  
Author(s):  
M. Jurzysta ◽  
S. Burda ◽  
W. Oleszek ◽  
M. Ploszynski
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Leaf Tissue ◽  
Taxonomic Position ◽  
Chemical Affinity ◽  
Chemical Markers ◽  
Plant Kingdom ◽  
Medicagenic Acid ◽  
Layer Chromatography

Flavonoids from fresh flowers of 35 species and medicagenic acid from leaf tissue of 44 species of the tribe Trigonelleae Schulz (Fabaceae) were examined using thin-layer chromatography. Moreover, medicagenic acid glycosides in the leaf tissue were also analyzed by the hemolytic test. Compounds tentatively identified as kaempferol, quercetin, myricetin, laricytrin, and medicagenic acid were present in hydrolysates of all species of the genus Medicago, including five species of debated taxonomic position, M. radiata, M. hybrida, M. cretacea, M. arborea, and M. lupulina. Laricytrin and medicagenic acid, while rarely occurring in the plant kingdom, may be regarded as chemical markers that distinguish the genus Medicago in Trigonelleae and may further support the placement of the five questionable species into Medicago. Laricytrin and medicagenic acid were also found in hydrolysates of three species of the section Buceras of the genus Trigonella (T. monantha, T. monspeliaca, and T. polyceratia) and were not found in any of the remaining tested species of Trigonella or in the genus Melilotus. This chemical affinity of the three Trigonella species to Medicago gives further support to the placement of these species in genus Medicago.

scholarly journals Isolation and chemical characterization of saponins from lucerne seeds (Medicago media Pers.)

2015 ◽  
Vol 42 (2) ◽  
pp. 201-207 ◽  
Author(s):  
Marian Jurzysta
Keyword(s):  
Thin Layer ◽  
Red Blood Cells ◽  
Thin Layer Chromatography ◽  
Blood Cells ◽  
Glucuronic Acid ◽  
Chemical Characterization ◽  
Acid Hydrolysate ◽  
Medicagenic Acid ◽  
Layer Chromatography

Saponins of lucerne seeds have been prepared by two different methods. It was found by thin-layer chromatography that these glycosides consist of at least four components with one dominant. Soyasapogenols B, C and E were identified in acid hydrolysate of these saponins and in carbohydrate moiety glucose, galactose, rhamnose, small quantity of arabinose and xylose and glucuronic acid. It was established that saponins of lucerne seeds do not haemolyse red blood cells, contrary to top, root and blossom saponins. That may be due to the lack of medicagenic acid glycosides.

Thin-Layer Chromatography

1965 ◽  
Author(s):  
H. R. Bolliger ◽  
M. Brenner ◽  
H. Gänshirt ◽  
Helmut K. Mangold ◽  
H. Seiler ◽  
...  
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Layer Chromatography

THE LESS-POLAR METABOLITES PRODUCED BY INCUBATION OF TESTOSTERONE-4-14C WITH RAT AND BOVINE BRAIN

1969 ◽  
Vol 61 (4) ◽  
pp. 641-648 ◽  
Author(s):  
Leon J. Sholiton ◽  
Emile E. Werk
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Paper Chromatography ◽  
Specific Activity ◽  
Bovine Brain ◽  
Polar Fraction ◽  
End Products ◽  
Polar Metabolites ◽  
Layer Chromatography ◽  
Constant Specific Activity

ABSTRACT Rat and bovine brain have been incubated with testosterone-4-14C under standard conditions. With use of paper chromatography, the extracted metabolites were noted to fall into less-polar, iso-polar, and more polar fractions. The components of the less-polar fraction were separated by acetylation and thin-layer chromatography and the major end-products identified by recrystallization to constant specific activity or constant 3H/14C ratios. Androst-4-enedione and 5α-dihydrotestosterone were formed consistently under the conditions utilized. Trace amounts of other less-polar metabolites were noted occasionally.

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