Vitro antitumor activity and synthesis of the key intermediate of bakuchiol / 药学学报
Acta Pharmaceutica Sinica
; (12): 467-470, 2010.
Article
en Zh
| WPRIM
| ID: wpr-353374
Biblioteca responsable:
WPRO
ABSTRACT
The in vitro antitumor activity of bakuchiol was exploited, compared with tamoxifen. The result of biological activities showed that bakuchiol could inhibit human breast cancer and the IC50 values were 2.89 x 10(-5) mol L(-1) and 8.29 x 10(-3) mol L(-1) against the cells line T-47D and MDA-MB-231 respectively. On the other hand, the key intermediate to synthesize bakuchiol was obtained by the method of Ireland-Claisen rearrangement. Comparing with traditional Claisen rearrangement, the reaction conditions are milder and the reaction reagents are safer.
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Patología
/
Farmacología
/
Fenoles
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Plantas Medicinales
/
Tamoxifeno
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Neoplasias de la Mama
/
Química
/
Antineoplásicos Hormonales
/
Concentración 50 Inhibidora
/
Psoralea
Límite:
Female
/
Humans
Idioma:
Zh
Revista:
Acta Pharmaceutica Sinica
Año:
2010
Tipo del documento:
Article