RESUMEN
Dihydrochelerythrine was isolated from the ethanol extract of Corydalis yanhusuo by chromatographic and recrystallization techniques. To our knowledge, this is the first report that dihydrochelerythrine was found to be unstable. The NMR, HPLC, and LC-MS were applied to monitor the structural conversion process of dihydrochelerythrine. The results showed that when dissolved in polar deuteration solvent (e.g., DMSO-₆ & MeOD), dihydrochelerythrine is directly converted to chelerythrine gradually. However, if used non-polar reagent (e.g.,CD₂Cl₂), the sample of dihydrochelerythrine undergoes the formation of pseudobase, chelerythrine, and bimolecular ether then followed by oxidation to oxychelerythrine as the major final product. Which leads to this phenomenon maybe is that the C-6 in dihydrochelerythrine is highly reactive to nucleophiles, and is easily converted to different derivatives in different solvents attributed to the solvent effect. This finding will contribute to the extraction and isolation, bioactivity screening, and quality evaluation of medicinal materials containing dihydrochelerythrine and other similar derivatives.
RESUMEN
Objective To study the anti-HBV constituents from Corydalis saxola. Methods The constituents were repeatedly purified by column chromatography and were identified on the basis of spectral analysis and comparison of their spectral data with those previously reported. Compounds isolated in large amounts were assayed against HBV. Results Sixteen compounds were identified to be dihydrosanguinarine (1), d-corydaline (2), cavidine (3), stylopine (4), 6-acetonyl-5, 6-dihydrosanguinarine (5), dihydrochelerythrine (6), tetrahydropalmatine (7), adlumidine (8), (-)-salutaridine (9), palmatine (10), protopine (11), berberine (12), coptisine (13), thalifaurine (14), dehydroapocavidine (15), and (+)-magnoflorine (16). Compounds 5, 6, 8-11, 13, and 16 with high amounts were chosen to detect anti-HBV activities. Compounds 5 and 8 were moderately active, compounds 11 and 16 showed weak inhibitory effects, while compound 6 exihibited the most potent activity against HBsAg and HBeAg secretions in HepG 2.2.15 cell line, followed by compound 9. Conclusion Compounds 1, 4-6, 8, 9, 13, 14, and 16 are isolated from C. saxicola for the first time. Compound 10 is the main constituent and compound 6 exihibits the most potent activity against HBV.
RESUMEN
Com o aumento da resistência bacteriana aos antibióticos disponíveis, tornou-se imprescindível a busca por novos fármacos ou protótipos. Os metabólitos secundários produzidos por alguns vegetais como cumarinas, alcaloides e terpenoides podem apresentar várias atividades biológicas, dentre elas, atividade antibiótiotica. O objetivo deste trabalho foi avaliar a atividade antimicrobiana in vitro, pelo método de difusão em disco, das diferentes partes de duas espécies pertencentes à família Rutaceae coletadas na Chapada Diamantina, Bahia, Brasil: Spiranthera odoratissima A. St.-Hil. e Zanthoxylum stelligerum Turcz., bem como do alcaloide diidroqueleritrina, isolado do extrato metanólico de Z. stelligerum frente a cepas padrão de microrganismos e isolados clínicos. Os resultados apresentados indicam que o extrato da raiz da espécie Z. stelligerum e o alcaloide extraído desta apresentaram propriedades antimicrobianas contra as cepas Gram positivas e leveduras. A E. coli foi a única cepa Gram negativa que se mostrou sensível ao extrato e ao alcaloide.
With the increase in bacterial resistance to available antibiotics, it became imperative to search for new drugs or prototypes. The secondary metabolites produced by some plants as coumarins, alkaloids and terpenoids have several biological activities, among them, antibiotic activity. The objective of this study was to evaluate the antimicrobial activity in vitro by the disk diffusion method, from different parts of two species belonging to the family Rutaceae, collected in the Chapada Diamantina, Bahia, Brazil: Spiranthera odoratissima A. St Hil. and Zanthoxylum stelligerum Turcz., and the alkaloid dihydrochelerythrine, isolated from the methanolic extract of Z. stelligerum front of standard strains of microorganisms and clinical isolates. The results indicate that the extract from the roots of Z. stelligerum and the alkaloid had antimicrobial properties against Gram positive and yeast strains. The E. coli was the only Gram negative strain that was sensitive to extract and the alkaloid.