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ApoE secretion modulating bromotyrosine derivative from the Australian marine sponge Callyspongia sp.
Affiliation:1. Eskitis Institute, Griffith University, Brisbane, QLD 4111, Australia;2. Centre for Drug Research and Development, Vancouver, BC V6T 1Z3, Canada;3. Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC V6T 1Z4, Canada;4. Queensland Museum, South Brisbane, QLD 4101, Australia
Abstract:High throughput screening of a pre-fractionated natural product library identified 11 active fractions showing ApoE modulation activity. Mass-directed fractionation of one active crude extract from the Australian marine sponge Callyspongia sp. resulted in the isolation of 13 metabolites, including three new bromotyrosine derivatives, callyspongic acid (1), 3,5-dibromo-4-methoxyphenylpyruvic acid (2), N-acetyl-3-bromo-4-hydroxylphenylethamine (3), and ten known compounds (413). The structure elucidation of compounds 13 was based on their 1D and 2D NMR and MS spectroscopic data. 3,5-Dibromo-4-methoxyphenylpyruvic acid (2) showed weak activity in increasing the apolipoprotein E secretion from human CCF-STTG1 cells at the concentration of 40 μM.
Keywords:Bromotyrosine derivatives  Bastadin  ApoE modulation activity
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