Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros




Base de datos
Intervalo de año de publicación
1.
Phytochemistry ; 224: 114140, 2024 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-38750709

RESUMEN

Eight previously undescribed cevanine-type steroidal alkaloids, cirrhosinones I-N and cirrhosinols A-B, along with five known analogs, were isolated from the bulbs of Fritillaria cirrhosa D. Don. Their structures were elucidated on the basis of comprehensive analysis of HRESIMS, 1D and 2D NMR spectroscopic data, and single-crystal X-ray diffraction analyses. All compounds revealed weak NO inhibitory activities in the LPS-stimulated NR8383 cells at the concentration of 20 µM, with inhibition ratios ranging from 5.1% to 14.3%.


Asunto(s)
Alcaloides , Fritillaria , Raíces de Plantas , Fritillaria/química , Raíces de Plantas/química , Estructura Molecular , Alcaloides/química , Alcaloides/aislamiento & purificación , Alcaloides/farmacología , Cevanas/química , Cevanas/farmacología , Cevanas/aislamiento & purificación , Óxido Nítrico/antagonistas & inhibidores , Óxido Nítrico/biosíntesis , Lipopolisacáridos/farmacología , Lipopolisacáridos/antagonistas & inhibidores , Animales , Conformación Molecular , Cristalografía por Rayos X , Línea Celular , Ratas , Esteroides/química , Esteroides/aislamiento & purificación , Esteroides/farmacología , Relación Dosis-Respuesta a Droga , Relación Estructura-Actividad , Modelos Moleculares
2.
Steroids ; 181: 108977, 2022 05.
Artículo en Inglés | MEDLINE | ID: mdl-35134432

RESUMEN

Seven undescribed steroidal alkaloids, including two jervine-type steroidal alkaloids, fritiunibras A-B (1-2), and five cevanine-type steroidal alkaloid glycosides, fritiunibras C-G (3-7), along with six known cevanine-type steroidal alkaloids and their glycosides (8-13) were isolated from the bulbs of Fritillaria unibracteata Hsiao et K. C. Hsia. Their structures were determined by interpretation of comprehensive spectroscopic and single-crystal X-ray diffraction analysis. The absolute configurations of sugar moieties were determined by HPLC analysis and compared with standards after hydrolysis and derivatization. Furthermore, their inhibitory effects on NO production and cytotoxic activities were evaluated.


Asunto(s)
Alcaloides , Fritillaria , Alcaloides/química , Alcaloides/farmacología , Fritillaria/química , Glicósidos/farmacología , Estructura Molecular , Esteroides/química
3.
Parasitol Res ; 112(3): 1197-203, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23271568

RESUMEN

The aim of this research was to determine larvicidal activity of the essential oil derived from roots of Toddalia asiatica (L.) Lam. and the isolated constituents against the larvae of the Culicidae mosquito Aedes albopictus. Essential oil of T. asiatica roots was obtained by hydrodistillation and analyzed by GC and GC-MS. A total of 58 components of the essential oil of T. asiatica roots were identified. The essential oil has almost same content of (35.41 %) of sesquiterpenoids and monoterpenoids (31.87 %). The principal compounds in T. asiatica essential oil were geraniol (9.84 %), D-limonene (7.52 %), isopimpinellin (6.62 %), α-gurjunene (6.25 %), and 4-vinylguaiacol (5.94 %). Based on bioactivity-directed fractionation, geraniol, D-limonene, and isopimpinellin were isolated from T. asiatica root essential oil. Geraniol, D-limonene, and isopimpinellin exhibited strong larvicidal activity against A. albopictus with LC(50) values of 30.13, 19.84, and 32.05 µg/ml, respectively, while the essential oil of T. asiatica had an LC(50) value of 69.09 µg/ml. The result indicated that the essential oil of T. asiatica roots and the three isolated constituents have potential for use in control of A. albopictus larvae and could be useful in search of newer, safer, and more effective natural compounds as larvicides.


Asunto(s)
Aedes/efectos de los fármacos , Insecticidas/farmacología , Aceites Volátiles/análisis , Aceites Volátiles/farmacología , Rutaceae/química , Animales , Bioensayo , Cromatografía de Gases y Espectrometría de Masas , Insecticidas/química , Insecticidas/aislamiento & purificación , Larva/efectos de los fármacos , Aceites Volátiles/aislamiento & purificación , Raíces de Plantas/química , Análisis de Supervivencia
4.
Molecules ; 17(12): 14870-81, 2012 Dec 13.
Artículo en Inglés | MEDLINE | ID: mdl-23519259

RESUMEN

The aim of this research was to determine chemical composition and insecticidal activity of the essential oil of Illicium pachyphyllum fruits against two grain storage insects, Sitophilus zeamais and Tribolium castaneum, and to isolate any insecticidal constituents from the essential oil. The essential oil of I. pachyphyllum fruits was obtained by hydrodistillation and analyzed by GC-MS. A total of 36 components of the essential oil were identified, with the principal compounds in the essential oil being trans-ρ-mentha-1(7),8-dien-2-ol (24.56%), D-limonene (9.79%), caryophyllene oxide (9.32%), and cis-carveol (5.26%) followed by ß-caryophyllene (4.63%) and bornyl acetate. Based on bioactivity-guided fractionation, the three active constituents were isolated and identified as trans-ρ-mentha-1(7),8-dien-2-ol, D-limonene and caryophyllene oxide. The essential oil of I. pachyphyllum fruits exhibited contact toxicity against S. zeamais and T. castaneum adults, with LD(50) values of 17.33 µg/adult and 28.94 µg/adult, respectively. trans-p-Mentha-1(7),8-dien-2-ol (LD(50) = 8.66 µg/adult and 13.66 µg/adult, respectively) exhibited stronger acute toxicity against S. zeamais and T. castaneum adults than either caryophyllene oxide (LD(50) = 34.09 µg/adult and 45.56 µg/adult) and D-limonene (LD(50) = 29.86 µg/adult and 20.14 µg/adult). The essential oil of I. pachyphyllum possessed fumigant toxicity against S. zeamais and T. castaneum adults with LC(50) values of 11.49 mg/L and 15.08 mg/L, respectively. trans-p-Mentha-1(7),8-dien-2-ol exhibited stronger fumigant toxicity against S. zeamais and T. castaneum adults, respectively, with LC(50) values of 6.01 mg/L and 8.14 mg/L, than caryophyllene oxide (LC(50) = 17.02 mg/L and 15.98 mg/L) and D-limonene (LC(50) = 33.71 mg/L and 21.24 mg/L). The results indicate that the essential oil of I. pachyphyllum fruits and its constituent compounds have potential for development into natural insecticides or fumigants for the control of insects in stored grains.


Asunto(s)
Frutas/química , Illicium/química , Insecticidas/química , Aceites Volátiles/química , Animales , Canfanos/análisis , Canfanos/química , Canfanos/farmacología , Monoterpenos Ciclohexánicos , Ciclohexenos/análisis , Ciclohexenos/química , Ciclohexenos/farmacología , Grano Comestible , Conservación de Alimentos , Almacenamiento de Alimentos , Cromatografía de Gases y Espectrometría de Masas , Concentración 50 Inhibidora , Insecticidas/análisis , Insecticidas/farmacología , Limoneno , Monoterpenos/análisis , Monoterpenos/química , Monoterpenos/farmacología , Aceites Volátiles/análisis , Aceites Volátiles/farmacología , Sesquiterpenos Policíclicos , Sesquiterpenos/análisis , Sesquiterpenos/química , Sesquiterpenos/farmacología , Terpenos/análisis , Terpenos/química , Terpenos/farmacología , Tribolium/efectos de los fármacos , Gorgojos/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA