Pan Fen-Cong, Liu Han-Fei, Shu Xiao-Die, Yang Xiao-Qiao, Lou Hua-Yong, Pan Wei-Dong, Zhang Ni, Li Jin-Yu
State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University, Baijin Road No.3491, Guiyang, 550014, China; Natural Products Research Center of Guizhou Province, Baijin Road No.3491, Guiyang, 550014, China.
State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University, Baijin Road No.3491, Guiyang, 550014, China.
Phytochemistry. 2025 Sep;237:114517. doi: 10.1016/j.phytochem.2025.114517. Epub 2025 Apr 25.
Saleucanes A-J (1-10), ten unprecedented neo-clerodane diterpenoids, and twenty-two knowns were isolated from the whole plant of Salvia leucantha. Their structures including absolute configurations were elucidated by extensive spectroscopic methods, single-crystal X-ray crystallographic and ECD calculation. Compound 7 possesses an unusual 6/5/6/4/6/5-hexacyclic fused ring skeleton, with a rare oxetane unit. All compounds were evaluated for their inhibitory effect on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in BV-2 cells. The results showed that five compounds exhibited significant NO inhibitory effects, with IC values ranging from 3.29 to 6.65 μM, which were better than the positive control minocycline hydrochloride (IC = 18.81 μM). Among them, compound 5 showed significant inhibitory effect, which significantly suppressed the production of IL-6, IL-1β, and TNF-α, as well as iNOS and COX-2 in a concentration-dependent manner. Further investigation results showed that compound 5 exerts anti-inflammatory effect via the TLR4/MYD88/NF-κB signaling pathway. To summarize, these findings supported the great hope of compound 5 as a potential novel inhibitor of neuroinflammation.
从白花丹参全草中分离得到了10个前所未有的新克罗烷二萜类化合物萨鲁卡内斯A-J(1-10)以及22个已知化合物。通过广泛的光谱方法、单晶X射线晶体学和ECD计算阐明了它们的结构,包括绝对构型。化合物7具有不寻常的6/5/6/4/6/5-六环稠合环骨架,并带有一个罕见的氧杂环丁烷单元。对所有化合物进行了评估,考察其对BV-2细胞中脂多糖(LPS)诱导的一氧化氮(NO)生成的抑制作用。结果表明,5个化合物表现出显著的NO抑制作用,IC值范围为3.29至6.65 μM,优于阳性对照盐酸米诺环素(IC = 18.81 μM)。其中,化合物5表现出显著的抑制作用,以浓度依赖性方式显著抑制IL-6、IL-1β和TNF-α以及诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的生成。进一步的研究结果表明,化合物5通过TLR4/MYD88/NF-κB信号通路发挥抗炎作用。总之,这些发现支持了化合物5作为神经炎症潜在新型抑制剂的巨大希望。