Antioxidant dehydrotocopherols as a new chemical character of Stemona species

Abstract

From the roots of various Stemona species four new dehydrotocopherols (chromenols) were isolated and their structures and stereochemistry elucidated by spectroscopic methods. The double bond between C-3 and C-4 proved to be a typical chemical character of the genus found in most of the species. Various C-methylations of the aromatic ring reflect differences in methyltransferase activities and agreed with the current species delimitations showing an exclusive accumulation of dehydro-δ-tocopherol for the Stemona tuberosa group, whereas different provenances of Stemona curtisii were characterized by dehydro-γ-tocopherol accompanied by small amounts of dehydro-α-tocopherol. From Stemona collinsae all four tocopherols were isolated with a clear preponderance of dehydro-δ-tocopherol accompanied by smaller amounts of the rare dehydro-β-tocopherol. Stemona burkillii and a group of unidentified species showed a weak accumulation trend towards dehydro-α-tocopherol, whereas Stemona cochinchinensis and especially Stemona kerrii clearly differed by a preponderance of chromanol derivatives. In Stemona cf. pierrei no tocopherols could be detected at all. Based on TLC tests and microplate assays with the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH ) the antioxidant capacities of all chromenol derivatives were comparable with that of α-tocopherol showing no significant differences among each other, except for a more rapid kinetic behaviour of the 5,7,8-methylated dehydro-α-tocopherol.