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1.
Nat Prod Res ; 30(14): 1591-7, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26710827

RESUMEN

A new alkylated coumarin derivative, hexapetarin (1) along with three other xanthones, trapezifolixanthone (2), cudraxanthone G (3) and 1,3,7-trihydroxy-2,4-di (3-methyl-2-butenyl)xanthone (4), and four common triterpenoids, friedelin (5), stigmasterol (6), beta-sitosterol (7) and gamma-sitosterol (8) were isolated from the stem bark of Mesua hexapetala (Clusiaceae), a plant, native to Malaysia. The structures of these compounds were elucidated and determined using spectroscopic techniques such as NMR and MS. Anti-inflammatory activity assay indicated hexapetarin (1) to possess moderate anti-inflammatory activity, while 1,3,7-trihydroxy-2,4-di (3-methyl-2-butenyl)xanthone (4) gave very good activity.


Asunto(s)
Clusiaceae/química , Cumarinas/química , Corteza de la Planta/química , Tallos de la Planta/química , Antiinflamatorios no Esteroideos/farmacología , Células Cultivadas , Cumarinas/farmacología , Humanos , Espectroscopía de Resonancia Magnética , Malasia , Espectrometría de Masas , Extractos Vegetales/química , Espectrofotometría Infrarroja , Espectrofotometría Ultravioleta
2.
Nat Prod Res ; 28(19): 1534-8, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24897077

RESUMEN

A new coumarin, hoseimarin (1), together with four other xanthones, trapezifolizanthone (2), osajaxanthone (3), ß-mangostin (4) and caloxanthone A (5), were isolated from the stem bark of Calophyllum hosei. The structures of these compounds were established by using spectroscopic analysis which included (1)H NMR, (13)C NMR, COSY, DEPT, HMQC and HMBC experiments.


Asunto(s)
Antiinflamatorios/aislamiento & purificación , Calophyllum/química , Cumarinas/aislamiento & purificación , Plantas Medicinales/química , Animales , Antiinflamatorios/química , Antiinflamatorios/farmacología , Cumarinas/química , Cumarinas/farmacología , Isoflavonas/química , Isoflavonas/aislamiento & purificación , Lipopolisacáridos/farmacología , Macrófagos/efectos de los fármacos , Ratones , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Corteza de la Planta/química , Xantonas/química , Xantonas/aislamiento & purificación
3.
J Asian Nat Prod Res ; 10(5-6): 475-9, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18464091

RESUMEN

Our current interest in searching for natural anti-cancer lead compounds from plants has led us to the discovery that the stem and roots of Garcinia mangostana can be a source of such compounds. The stem furnished 2,8-dihydroxy-6-methoxy-5-(3-methylbut-2-enyl)-xanthone (1), which is a new xanthone. Meanwhile, the root bark of the plant furnished six xanthones, namely alpha-mangostin (2), beta-mangostin (3), gamma-mangostin (4), garcinone D (5), mangostanol (6), and gartanin (7). The hexane and chloroform extracts of the root bark of G. mangostana as well as the hexane extract of the stem bark were found to be active against the CEM-SS cell line. gamma-Mangostin (4) showed good activity with a very low IC(50) value of 4.7 microg/ml, while alpha-mangostin (2), mangostanol (6), and garcinone D (5) showed significant activities with IC(50) values of 5.5, 9.6, and 3.2 microg/ml, respectively. This is the first report on the cytotoxicity of the extracts of the stem and root bark of G. mangostana and of alpha-mangostin, mangostanol, and garcinone D against the CEM-SS cell line.


Asunto(s)
Antineoplásicos Fitogénicos/aislamiento & purificación , Garcinia mangostana/química , Xantonas/aislamiento & purificación , Antineoplásicos Fitogénicos/farmacología , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Humanos , Estructura Molecular , Corteza de la Planta/química , Extractos Vegetales/farmacología , Xantonas/química , Xantonas/farmacología
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