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塔拉尔霉素 A-F:来源于节肢动物内生真菌塔马尔氏青霉的呋甾烷二萜。

Talarmalnoids A-F: Fusicoccane diterpenoids from an arthropod-derived endophytic fungus Talaromyces malicola.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China.

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China.

出版信息

Fitoterapia. 2024 Dec;179:106262. doi: 10.1016/j.fitote.2024.106262. Epub 2024 Oct 23.

Abstract

The metabolites from the endophytic fungus Talaromyces malicola hosted in the gastrointestinal tract of the arthropods Armadillidium vulgare were investigated, and six undescribed fusicoccane diterpenoids, talarmalnoids A-F (1-6), along with three known analogs were isolated. Talarmalnoid C (3) was an unprecedented fusicoccane diterpenoid with two sugar units, i.e., 6-O-methyl-α-d-glucose and α-d-glucose. Talarmalnoids D and E (4 and 5) were fusicoccane-type diterpenoids with unusual seven-membered rings attached at the C-3' and C-4' positions. Their structures and absolute configurations were identified by NMR, HRESIMS analyses, X-ray single crystal diffraction, GC-MS, ECD analyses, C NMR calculations, and DP4+ probability analyses. Bioassay results showed that talarmalnoid B (2) exhibited significant inhibitory activities against the LPS-inducted production of NO in RAW 264.7 cells, with IC value of 0.83 μM.

摘要

对节肢动物犰狳卷甲虫胃肠道内生真菌塔玛多毛孢中代谢产物进行了研究,从中分离得到了 6 个未描述的呋甾烷二萜类化合物,即塔拉霉素 A-F(1-6),以及 3 个已知类似物。塔拉霉素 C(3)是一种具有两个糖单元,即 6-O-甲基-α-d-葡萄糖和α-d-葡萄糖的前所未有的呋甾烷二萜类化合物。塔拉霉素 D 和 E(4 和 5)是具有异常七元环的呋甾烷型二萜类化合物,分别连接在 C-3'和 C-4'位置。通过 NMR、HRESIMS 分析、X 射线单晶衍射、GC-MS、ECD 分析、C NMR 计算和 DP4+概率分析确定了它们的结构和绝对构型。生物测定结果表明,塔拉霉素 B(2)对 LPS 诱导的 RAW 264.7 细胞中 NO 的产生具有显著的抑制活性,IC 值为 0.83 μM。

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