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1.
Mem Inst Oswaldo Cruz ; 104(6): 813-7, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19876552

RESUMEN

Three Plumbago spp have been tested for mosquito larvicidal activity. The crude extracts exhibiting the highest larvicidal activity against Anopheles gambiae were hexane (LC50 = 6.4 microg/mL) and chloroform (LC50 = 6.7 microg/mL) extracts from Plumbago zeylanica Linn, chloroform (LC50 = 6.7 ug/mL) extract from Plumbago stenophylla Bull and ethyl acetate (LC50 = 4.1 microg/mL) extract from Plumbago dawei Rolfe. These LC50 values were within 95% confidence limits. 5-hydroxy-2-methyl-1,4-naphthoquinone (plumbagin) 1 (LC50 = 1.9 microg/mL) and beta-sitosterol 2 were characterised from ethyl acetate extract of root bark of P. dawei, a native medicinal plant growing in Kenya, based on spectral analysis and comparisons with data in literature.


Asunto(s)
Anopheles , Insecticidas , Extractos Vegetales/farmacología , Plumbaginaceae/química , Animales , Larva/efectos de los fármacos , Plumbaginaceae/clasificación
2.
Mem. Inst. Oswaldo Cruz ; 104(6): 813-817, Sept. 2009. ilus, tab
Artículo en Inglés | LILACS | ID: lil-529551

RESUMEN

Three Plumbago spp have been tested for mosquito larvicidal activity. The crude extracts exhibiting the highest larvicidal activity against Anopheles gambiae were hexane (LC50 = 6.4 μg/mL) and chloroform (LC50 = 6.7 μg/mL) extracts from Plumbago zeylanica Linn, chloroform (LC50 = 6.7 ug/mL) extract from Plumbago stenophylla Bull and ethyl acetate (LC50 = 4.1 μg/mL) extract from Plumbago dawei Rolfe. These LC50 values were within 95 percent confidence limits. 5-hydroxy-2-methyl-1,4-naphthoquinone (plumbagin) 1 (LC50 = 1.9 μg/mL) and β-sitosterol 2 were characterised from ethyl acetate extract of root bark of P. dawei, a native medicinal plant growing in Kenya, based on spectral analysis and comparisons with data in literature.


Asunto(s)
Animales , Anopheles , Insecticidas , Extractos Vegetales/farmacología , Plumbaginaceae/química , Larva/efectos de los fármacos , Plumbaginaceae/clasificación
3.
Planta Med ; 68(7): 615-20, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12142995

RESUMEN

A new isoflavanone namely 3,5,7,2',4'-pentahydroxy-8,3'-di(gamma,gamma-dimethylallyl)isoflavanone (bolusanthin II) and four new pterocarpans identified as 3-hydroxy-6',6'-dimethylpyrano[2',3':1,2] [6a R,11a R]-8,9-methylenedioxypterocarpan (bolucarpan A), 3-hydroxy-6',6'-dimethyl-4',5'-dihydropyrano[2',3':1,2][6a R,11a R]- 8,9-methylenedioxypterocarpan (bolucarpan B), 3-hydroxy-9-methoxy-6',6'-dimethylpyrano-[2',3':1,2][6a R,11a R]-pterocarpan (bolucarpan C) and 3-hydroxy-9-methoxy-6',6'-dimethyl-4',5'-dihydropyrano[2',3':1,2][6a R,11a R]-pterocarpan (bolucarpan D) and three known isoflavonoids were isolated from the methanolic extracts of the root bark, while eight known isoflavonoids were isolated from the stem bark of Bolusanthus speciosus. These compounds showed antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Saccharomyces cerevisiae and Candida mycoderma using the agar overlay technique.


Asunto(s)
Antiinfecciosos/farmacología , Fabaceae/química , Flavonoides/farmacología , Antibacterianos , Antiinfecciosos/química , Antiinfecciosos/aislamiento & purificación , Bacillus subtilis/efectos de los fármacos , Escherichia coli/efectos de los fármacos , Flavonoides/química , Flavonoides/aislamiento & purificación , Pruebas de Sensibilidad Microbiana , Conformación Molecular , Saccharomyces cerevisiae/efectos de los fármacos
4.
Planta Med ; 68(7): 640-2, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12143000

RESUMEN

The seed pods of Erythrina latissima yielded erysotrine, erysodine, syringaresinol, vanillic acid, a new erythrina alkaloid, (+)-10,11-dioxoerysotrine, which was lethal to brine shrimp and 2-(5'-hydroxy-3'-methoxy phenyl)-6-hydroxy-5-methoxybenzofuran, which showed strong antimicrobial activity against the yeast spores, Gram-positive and Gram-negative bacteria. The root bark gave four known pterocarpans which showed moderate to strong antifungal activity against the yeast spores and three known flavonoids showed antimicrobial activity against all test microorganisms.


Asunto(s)
Antiinfecciosos/farmacología , Benzofuranos/farmacología , Erythrina/química , Flavonoides/farmacología , Alcaloides/química , Alcaloides/aislamiento & purificación , Alcaloides/farmacología , Antibacterianos , Antiinfecciosos/química , Antiinfecciosos/aislamiento & purificación , Benzofuranos/química , Benzofuranos/aislamiento & purificación , Escherichia coli/efectos de los fármacos , Flavonoides/química , Flavonoides/aislamiento & purificación , Pruebas de Sensibilidad Microbiana , Pseudomonas aeruginosa/efectos de los fármacos , Saccharomyces cerevisiae/efectos de los fármacos , Staphylococcus aureus/efectos de los fármacos
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