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1.
Nat Prod Res ; 36(23): 5991-5998, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-35369818

RESUMEN

Chemical investigation of the MeOH extract of the leaves of Scyphocephalium mannii (Benth. & Hook.f.) Warb. (Myristicaceae) led to the isolation and characterization of one new metabolite (+)-(7'S, 8S, 8'S)-4,4'-dihydroxy-3,3',5,5'-tetramethoxy-2,7'-cyclolignan (1) along with five known compounds. Their structures were elucidated by spectroscopic means, including 1 D and 2 D NMR, HRESI-MS and by comparison with published data. The absolute configuration of compound 1 was determined by single-crystal X-RAY diffraction. Compound 1 showed moderate antifungal activity against Cryptococcus neoformans with respective MIC and MMC values of 64 and 256 µg/mL.


Asunto(s)
Antiinfecciosos , Myristicaceae , Estructura Molecular , Espectroscopía de Resonancia Magnética , Hojas de la Planta , Antiinfecciosos/farmacología
2.
Nat Prod Res ; 32(1): 85-90, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28587572

RESUMEN

One new degraded diterpenoid 3,6-dihydroxy-1,7-dimethyl-9,10-phenantroquinone (neomacrodione) (1) together seven known compounds were isolated from the roots of Neoboutonia macrocalyx (Euphorbiaceae). The structures of the compounds were established based on their NMR and mass spectrometric data in conjunction with those previously reported in the literature. Compound (1) displayed moderate antibacterial activities.


Asunto(s)
Antibacterianos/química , Diterpenos/química , Euphorbiaceae/química , Fenantrenos/química , Antibacterianos/farmacología , Diterpenos/farmacología , Evaluación Preclínica de Medicamentos/métodos , Espectroscopía de Resonancia Magnética , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Fenantrenos/farmacología , Raíces de Plantas/química
3.
Rev. bras. farmacogn ; 27(2): 251-253, Mar.-Apr. 2017. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1042249

RESUMEN

ABSTRACT Four compounds including beauvericin, parahydroxybenzaldehyde, indole-3-carboxylic acid and quinizarin were isolated from endophytic fungus Epicoccum nigrum and their cytotoxicity, antibacterial and antioxidant activity were evaluated. Beauvericin had remarkable activity against two Gram-negative strains (Bacillus cereus and Salmonella typhimurium) with respective MIC values of 3.12 and 6.25 µg/ml. All the compounds had weak cytotoxic effect on both normal and tumor cells. LC50 values ranged from 40.42 to 86.56 µg/ml, 31.87 to 86.57 µg/ml and 21.59 to 67.27 µg/ml on Vero cells, THP-1 and RAW 264.7 respectively. The present study showed that these compounds could be developed for the formulation of antioxidant-rich therapeutic diets and as a therapeutic agent against bacterial infections.

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