RESUMEN
A new stigmasterol ester: stigmasterol tetracosanoate (3), along with 7 compounds: ß-sitosterol (1), stigmasterol (2), (2S,3S,4R)-2[(2'R)-2'-(hydroxyeicosanoyl amino) octadecane-1,3,4-triol (4), apigenin (5), ß-sitosterol-3-O-ß-D-glucopyranoside (6), stigmasterol-3-O-ß-D-glucopyranose (7), and apigenin-7-O-ß-D-glucopyranoside (8) were isolated from Blepharis ciliaris aerial parts. Compounds 1, 2, and 5-7 are reported here for the first time from the plant and 4 for the first time from the family. GCMS analysis revealed the presence of 45 fatty acids, 53 hydrocarbons, and 24 sterols. The different fractions exhibited mild cytotoxic in brine shrimp assay and anti-hyperglycaemic activities. The EtOAc fraction and TME (total MeOH extract) showed weak anti-malarial activity against P. falciparum. The CHCl3 fraction gave potent -anti-inflammatory activity compared with indomethacin.
Asunto(s)
Acanthaceae/química , Ésteres/aislamiento & purificación , Ésteres/farmacología , Ácidos Grasos/farmacología , Estigmasterol/análogos & derivados , Estigmasterol/aislamiento & purificación , Animales , Antiinflamatorios/aislamiento & purificación , Antiinflamatorios/farmacología , Antimaláricos/aislamiento & purificación , Antimaláricos/farmacología , Ácidos Grasos/aislamiento & purificación , Hipoglucemiantes/aislamiento & purificación , Hipoglucemiantes/farmacología , Masculino , Ratones , Estructura Molecular , Componentes Aéreos de las Plantas/química , Ratas , Estigmasterol/farmacologíaRESUMEN
A new pentacyclic oleanene triterpene, 2beta, 3beta, 16alpha, 28-tetrahydroxy-olean-12-ene-23-oic acid (1), as well as the known pentacyclic triterpene medicagenic acid (2), have been isolated by different chromatographic techniques from the acid hydrolysate of the saponin fraction of Gladiolus segetum. The identification of these compounds was established by different methods of physical, chemical and spectral evidence.
Asunto(s)
Iridaceae/química , Ácido Oleanólico/aislamiento & purificación , Saponinas/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura MolecularRESUMEN
An aqueous extract of mesocarps of the fruits of Balanites aegyptiaca exhibited a prominent antidiabetic activity by oral administration in streptozotocin induced diabetic mice. From one of the active fractions of this extract, two new steroidal saponins were isolated, and their structures were determined as 26-O-beta-D-glucopyranosyl-(25R)-furost-5-ene-3 beta,22,26-triol 3-O-[alpha-L-rhamnopyranosyl-(1----2)]-[beta-D-xylopyranosyl-(1---- 3)]-[alpha-L-rhamnopyranosyl-(1----4)]-beta-D-glucopyranoside and its 22-methyl ether. In addition, two known saponins, 26-O-beta-D-glucopyranosyl-(25R)-furost-5-ene-3 beta,22,26-triol 3-O-(2,4-di-O-alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside and its methyl ether were isolated and identified. It was revealed that the individual saponins did not show antidiabetic activity, while the recombination of these saponins resulted in significant activity. From an ethanolic extract of the epicarps, two known flavonol glycosides, isorhamnetin-3-O-robinobioside and isorhamnetin-3-O-rutinoside were isolated and identified.