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1.
Mar Drugs ; 20(2)2022 Feb 16.
Artículo en Inglés | MEDLINE | ID: mdl-35200673

RESUMEN

In this review, we summarized the distribution of the chemically investigated Oceanapia sponges, including the isolation and biological activities of their secondary metabolites, covering the literature from the first report in 1989 to July 2019. There have been 110 compounds reported during this period, including 59 alkaloids, 33 lipids, 14 sterols and 4 miscellaneous compounds. Besides their unique structures, they exhibited promising bioactivities ranging from insecticidal to antibacterial. Their complex structural characteristics and diverse biological properties have attracted a great deal of attention from chemists and pharmaceuticals seeking to perform their applications in the treatment of disease.


Asunto(s)
Productos Biológicos/aislamiento & purificación , Poríferos/metabolismo , Alcaloides/química , Alcaloides/aislamiento & purificación , Alcaloides/farmacología , Animales , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Productos Biológicos/química , Productos Biológicos/farmacología , Humanos , Insecticidas/química , Insecticidas/aislamiento & purificación , Insecticidas/farmacología , Lípidos/química , Lípidos/aislamiento & purificación , Lípidos/farmacología , Metabolismo Secundario , Esteroles/aislamiento & purificación , Esteroles/farmacología
2.
J Asian Nat Prod Res ; 14(2): 182-5, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22296160

RESUMEN

A new chiro-inositol ester, 4-hydroxyphenylacetyl-3-d-chiro-inositol ester (1), was isolated from the whole plants of Prenanthes macrophylla Franch., along with 10 known compounds, 4-hydroxyphenylacetic acid (2), trans-ethyl caffeate (3), cis-ethyl caffeate (4), protocatechualdehyde (5), luteolin (6), luteolin-7-O-ß-d-glucoside (7), 15-hydroxy-2-oxo-guai-3-en-1α,5α,6ß,7α,10α,11ßH-12,6-olide (8), 15-glucopyranosyloxy-2-oxo-guaia-3,11(13)-dien-1α,5α,6ß,7α,10αH-12,6-olide (9), ursolic acid (10), and oleanolic acid (11). Their structures were elucidated on the basis of spectroscopic analyses including HR-ESI-MS, ESI-MS, (1)H and (13)C NMR, HSQC, HMBC, and ROESY, and chemical evidences.


Asunto(s)
Asteraceae/química , Medicamentos Herbarios Chinos/aislamiento & purificación , Inositol/análogos & derivados , Inositol/aislamiento & purificación , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Inositol/química , Inositol/farmacología , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular
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