Browsing by Author "Bermejo, J."
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- Constituintes orgânicos do bivalve: Cerastoderma edulePublication . Matos, M.; Amado, J.; Rauter, A. P.; Samapayo, M.; Justino, Jorge; Bermejo, J.
- A new dihydroxysterol from the marine phytoplankton Diacronema sp.Publication . Rauter, A. P.; Filipe, M.M.; Prata, C.; Noronha, J.P.; Sampayo, M.A.M.; Justino, Jorge; Bermejo, J.Diacronema sp. was cultured and its sterols were separated by column chromatography on silica gel. The new sterol 24-ethyl-4α-methyl-cholestane-3,20-diol (1) was characterised by NMR and MS spectrometry, as well as (22E)-24-ethyl-4α-methyl-5α-cholest-22-en-3β-ol (2) and β-sitosterol, the major components of the sterol fractions. Neither the biosynthetic origin of the new dihydroxysterol nor its role in the biochemistry of Diacronema is known.
- A new lupene triterpenetriol and anticholinesterase activity of Salvia sclareoidesPublication . Rauter, A. P.; Branco, I.; Lopes, R. G.; Justino, Jorge; Silva, Filipa; Noronha, J. P.; Cabrita, E. J.; Brouard, I.; Bermejo, J.A new lupene triterpenetriol was isolated from the acetone extract of the aerial parts of Salvia sclareoides and characterised as (1β,3β)-lup-20(29)-ene-1,3,30-triol (1). In addition, nepetidin (2), nepeticin (3), lupendiol (4), (1β,11α)-dihydroxy-lup-20(29)-en-3-one (5), ursolic acid (6), sumaresinolic acid (7) and hederagenin (8), were identified in this Salvia sp. To the best of our knowledge, the compounds 2 and 7 are new constituents in Salvia spp. The acetone, ethanol, butanol and water extracts of the plant were screened for the in vitro inhibitory activity of acetylcholinesterase (AChE) and butyrilcholinesterase (BChE), enzymes which play a role in the Alzheimer disease. All extracts inhibited acetylcholinesterase activity at 10 μg/ml, a remarkable activity since the standard drug rivastigmine does not inhibit acetylcholinesterase at the same concentration. Regarding the butyrilcholinesterase, the acetone extract at 1000 μg/ml was able to inhibit completely the enzyme activity and the butanol and ethanol extracts, at this concentration, produced a potent inhibition of BchE.
- A novel pentacyclic triterpene from Leontodon filiiPublication . Tostão, Z.; Noronha, J.P.; Cabrita, E.J.; Medeiros, J.; Justino, Jorge; Bermejo, J.; Rauter, A. P.A novel oleanene triterpenetetrol was isolated from the chloroform extract of the aerial parts of Leontodon filii. Its structure was shown to be 2β,3β,15α,21β-olean-12-ene-2,3,15,21-tetrol by chemical and spectroscopic methods. The fungicidal efficacy of the chloroform and methanol extracts of the plant was also evaluated, a protective effect being found against Plasmopara viticola, Botrytis cinerea, particularly powerful against Pyricularia oryzae.