New cytotoxic tetrahydrofuran- and dihydrofuran-type lignans from the stem of Beilschmiedia tsangii

Planta Medica

Volumn 72, Issue 4, 2006, Pages 351-357

  Chen, Jih Jung ^a   Chou, En Tzu ^a   Duh, Chang Yih ^b   Yang, Sheng Zehn ^c   Chen, Ih Sheng ^d  

^a TAJEN UNIVERSITY   (Taiwan)

^b NATIONAL SUN YAT SEN UNIVERSITY   (Taiwan)

^c NATIONAL PINGTUNG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Taiwan)

^d KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

Author keywords

1 phenylbutyl benzoates; Beilschmiedia tsangii; Beilschmin A; Beilschmin B; Beilschmin C; Cytotoxicity; Dihydrofuran type lignan; Lauraceae; Tetrahydrofuran type lignans; Tsangin A; Tsangin B

Indexed keywords

2,6,11 TRIMETHYLDODECA 2,6,10 TRIENE; ALPHA TOCOPHERYLQUINONE; ALPHA TOCOSPIRO B; BEILSCHMIN A; BEILSCHMIN B; BEILSCHMIN C; BENZOIC ACID DERIVATIVE; DIHYDROFURAN; LIGNAN DERIVATIVE; PLANT EXTRACT; TETRAHYDROFURAN; TSANGIN A; TSANGIN B; UNCLASSIFIED DRUG;

ANGIOSPERM; ARTICLE; BEILSCHMIEDIA TSANGII; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; IN VITRO STUDY; PLANT; SPECTROSCOPY;

ANIMALS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; FURANS; HT29 CELLS; HUMANS; INHIBITORY CONCENTRATION 50; LAURACEAE; LIGNANS; MICE; PHYTOTHERAPY; PLANT EXTRACTS; PLANT STEMS; STRUCTURE-ACTIVITY RELATIONSHIP;

BEILSCHMIEDIA; LAURACEAE; MAGNOLIOPHYTA;

EID: 33645523496     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-916220     Document Type: Article

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