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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/45906

Title: Angiogenesis inhibitors and anti-inflammatory agents from Phoma sp. NTOU4195
Authors: Ming-Shian Lee;Shih-Wei Wang;Guei-Jane Wang;Ka-Lai Pang;Ching-Kuo Lee;Yueh-Hsiung Kuo;Hyo-Jung Cha;Ruo-Kai Lin;Tzong-Huei Lee
Contributors: 國立臺灣海洋大學:海洋生物研究所
Date: 2016
Issue Date: 2018-04-16T08:30:25Z
Publisher: Journal of Natural Products
Abstract: Abstract: Seven new polyketides, phomaketides A–E (1–5) and pseurotins A3 (6) and G (7), along with the known compounds FR-111142, pseurotins A, A1, A2, D, and F2, 14-norpseurotin A, α-carbonylcarbene, tyrosol, cyclo(-l-Pro-l-Leu), and cyclo(-l-Pro-l-Phe), were purified from the fermentation broth and mycelium of the endophytic fungal strain Phoma sp. NTOU4195 isolated from the marine red alga Pterocladiella capillacea. The structures were established through interpretation of spectroscopic data. The antiangiogenic and anti-inflammatory effects of 1–7 and related analogues were evaluated using human endothelial progenitor cells (EPCs) and lipopolysaccharide (LPS)-activated murine macrophage RAW264.7 cells, respectively. Of the compounds tested, compound 1 exhibited the most potent antiangiogenic activity by suppressing the tube formation of EPCs with an IC50 of 8.1 μM, and compound 3 showed the most selective inhibitory activity of LPS-induced NO production in RAW264.7 macrophages with an IC50 value of 8.8 μM.
Relation: 79(12)
URI: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/45906
Appears in Collections:[海洋生物研究所] 期刊論文

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