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Chem Pharm Bull (Tokyo) ; 55(4): 666-8, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17409569

ABSTRACT

Two 27C hydroperoxysterols, 7beta-hydroperoxycholesterol (1) and its stereoisomer 7alpha-hydroperoxycholesterol (2), were isolated from the lipophilic extracts of a Formosan tunicate belonging to the genus Eudistoma. The structures of sterols 1 and 2 were elucidated on the basis of extensive spectral data analyses. Cytotoxicity of sterols 1 and 2 against a limited panel of cancer cell lines is also described. Sterol 1 show weak inhibitory effects on human neutrophil elastase release.


Subject(s)
Sterols/isolation & purification , Urochordata/chemistry , Animals , Cell Line, Tumor , Chromatography, High Pressure Liquid , Drug Screening Assays, Antitumor , Humans , Magnetic Resonance Spectroscopy , Sterols/chemistry , Sterols/pharmacology
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