Glaucumolides A and B, Biscembranoids with New Structural Type from a Cultured Soft Coral Sarcophyton glaucum

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作者
Chiung-Yao Huang
Ping-Jyun Sung
Chokkalingam Uvarani
Jui-Hsin Su
Mei-Chin Lu
Tsong-Long Hwang
Chang-Feng Dai
Shwu-Li Wu
Jyh-Horng Sheu
机构
[1] National Sun Yat-sen University,Department of Marine Biotechnology and Resources
[2] National Museum of Marine Biology & Aquarium,Department of Medical Research
[3] Institute of Marine Biotechnology,undefined
[4] National Dong Hwa University,undefined
[5] Graduate Institute of Natural Products,undefined
[6] School of Traditional Chinese Medicine,undefined
[7] College of Medicine,undefined
[8] Chang Gung University,undefined
[9] Institute of Oceanography,undefined
[10] National Taiwan University,undefined
[11] General Study Center,undefined
[12] National Kaohsiung Marine University,undefined
[13] China Medical University Hospital,undefined
[14] China Medical University,undefined
[15] Graduate Institute of Natural Products,undefined
[16] Kaohsiung Medical University,undefined
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摘要
Glaucumolides A (1) and B (2), novel biscembranes composed of an unprecedented α,β-unsaturated ε-lactone, along with the known metabolites ximaolide A (3) and isosarcophytonolide D (4), were isolated from the cultured soft coral Sarcophyton glaucum. The structures of the new metabolites were determined by extensive spectroscopic analyses. Compounds 1 and 2 were shown to exhibit cytotoxicity against a limited panel of cancer cell lines. In anti-inflammation assay, compounds 1 and 2 displayed strong inhibition of superoxide anion generation and elastase release in human neutrophils stimulated by fMLP/CB. Furthermore, both 1 and 2 were shown to significantly inhibit the accumulation of the pro-inflammatory inducible nitric oxide synthase protein and compounds 1−3 were found to effectively reduce the expression of cyclooxygenase-2 protein, in lipopolysaccharide-stimulated RAW264.7 macrophage cells.
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