Chemical investigation of a marine-derived fungus, Penicillium steckii 108YD142, resulted in the discovery of a new tanzawaic acid derivative, tanzawaic acid Q (1), together with four known analogues, tanzawaic acids A (2), C (3), D (4), and K (5). The structures of tanzawaic acid derivatives 1-5 were determined by the detailed analysis of 1D, 2D NMR and LC-MS data, along with chemical methods and literature data analysis. These compounds significantly inhibited nitric oxide (NO) production and the new tanzawaic acid Q (1) inhibited the lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) proteins and mRNA expressions in RAW 264.7 macrophages. Additionally, compound 1 reduced the mRNA levels of inflammatory cytokines. Taken together, the results of this study demonstrated that the new tanzawaic acid derivative inhibits LPS-induced inflammation. This is the first report on the anti-inflammatory activity of tanzawaic acid Q (1).
Anti-Inflammatory Activity of Tanzawaic Acid Derivatives from a Marine-Derived Fungus Penicillium steckii 108YD142.
海洋真菌 Penicillium steckii 108YD142 的丹泽酸衍生物的抗炎活性
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作者:Shin Hee Jae, Pil Gam Bang, Heo Soo-Jin, Lee Hyi-Seung, Lee Jong Seok, Lee Yeon-Ju, Lee Jihoon, Won Ho Shik
| 期刊: | Marine Drugs | 影响因子: | 5.400 |
| 时间: | 2016 | 起止号: | 2016 Jan 8; 14(1):14 |
| doi: | 10.3390/md14010014 | 研究方向: | 炎症/感染 |
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