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1.
Mar Drugs ; 16(11)2018 Oct 25.
Artículo en Inglés | MEDLINE | ID: mdl-30366373

RESUMEN

One new neolignan, racelactone A (1), together with seven known compounds (2-8) were isolated from the methanolic extract of the leaves and twigs of Lumnitzera racemosa. The structure of racelactone A (1) was determined on the basis of the mass and NMR spectroscopic data interpretation. With respect to bioactivity, compound 1 displayed an anti-angiogenic effect by suppressing tube formation. Furthermore, compounds 1, 4, and 5 showed significant anti-inflammatory effects with IC50 values of 4.95 ± 0.89, 1.95 ± 0.40, and 2.57 ± 0.23 µM, respectively. The plausible biosynthesis pathway of racelactone A (1) was proposed.


Asunto(s)
Inhibidores de la Angiogénesis/química , Inhibidores de la Angiogénesis/farmacología , Antiinflamatorios/química , Antiinflamatorios/farmacología , Combretaceae/química , Lignanos/química , Lignanos/farmacología , Inhibidores de la Angiogénesis/aislamiento & purificación , Antiinflamatorios/aislamiento & purificación , Apoptosis/efectos de los fármacos , Avicennia , Células Progenitoras Endoteliales/efectos de los fármacos , Humanos , Lignanos/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Hojas de la Planta/química
2.
Mar Drugs ; 16(2)2018 Jan 31.
Artículo en Inglés | MEDLINE | ID: mdl-29385063

RESUMEN

Three new compounds, tuberazines A-C (1-3), and eleven known compounds (4-14) were obtained from the ethanolic extract of Taiwanese zoanthid Palythoa tuberculosa. Compounds 1-4 are rare marine natural products with a pyrazine moiety, and compound 5 is a tricyclic tryptamine derivative isolated from nature for the first time. The structures of all isolated metabolites were determined by analyzing their IR, Mass, NMR, and UV spectrometric data. The absolute configuration of 1 was confirmed by comparing the trend of experimental electronic circular dichroism (ECD) with calculated ECD spectra. The anti-lymphangiogenic activities of new compounds were evaluated in human lymphatic endothelial cells (LECs). Of these, new compound 3 displayed the most potent anti-lymphangiogenesis property by suppressing cell growth and tube formation of LECs.


Asunto(s)
Inhibidores de la Angiogénesis/farmacología , Antozoos/química , Linfangiogénesis/efectos de los fármacos , Animales , Antineoplásicos/farmacología , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Células Endoteliales/efectos de los fármacos , Humanos , Modelos Moleculares , Conformación Molecular , Taiwán , Extractos de Tejidos/farmacología
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