Konya Rima, Reis Rengin, Sipahi Hande, Barta Anita, Hohmann Judit, Kırmızıbekmez Hasan
Department of Pharmacognosy, Faculty of Pharmacy, Yeditepe University, Kayışdağı, İstanbul, Türkiye.
Department of Toxicology, Faculty of Pharmacy, Acibadem Mehmet Ali Aydinlar University, İstanbul, Türkiye.
Nat Prod Res. 2023 Aug-Sep;37(18):3025-3032. doi: 10.1080/14786419.2022.2144301. Epub 2022 Nov 8.
A previously unreported secoiridoid glycoside, cruciatoside () was isolated from the aerial parts of L. along with ten known compounds eustomoside (), eustomorusside (), gentiopicroside (), 6'--β-D-glucopyranosyl gentiopicroside (), loganic acid (), isoorientin (), isovitexin (), isovitexin 2''ferulate (), mangiferin (), and 2-methyl-inositol (). The chemical structures of the isolates were elucidated based on extensive 1 D and 2 D NMR experiments as well as HRMS analysis. All isolates were evaluated for their anti-inflammatory and analgesic activities. Compounds , , and (200 µM) showed moderate anti-inflammatory activity by inhibiting nitrite production from LPS-induced RAW 264.7 macrophage cells, with the inhibition rates of 39.5%, 25.8% and 22.9% respectively without exhibiting substantial cytotoxicity. Besides, , , , and exerted the highest decrease in IL-6 levels. Moreover, compound showed analgesic activity by decreasing the PGE level comparable to the reference drugs.
从**[植物名称未给出]**的地上部分分离出一种先前未报道的裂环烯醚萜苷,即十字花苷(),同时还分离出十种已知化合物,分别是常春花苷()、常春乌苏苷()、龙胆苦苷()、6'-O-乙酰基-β-D-吡喃葡萄糖基龙胆苦苷()、马钱子酸()、异荭草素()、异牡荆素()、异牡荆素2''-阿魏酸酯()、芒果苷()和2-甲基肌醇()。基于广泛的一维和二维核磁共振实验以及高分辨质谱分析,阐明了分离物的化学结构。对所有分离物进行了抗炎和镇痛活性评估。化合物、和(200µM)通过抑制脂多糖诱导的RAW 264.7巨噬细胞产生亚硝酸盐,显示出中等程度的抗炎活性,抑制率分别为39.5%、25.8%和22.9%,且未表现出明显的细胞毒性。此外,、、和使白细胞介素-6水平下降最多。此外,化合物通过降低前列腺素E水平显示出镇痛活性,与参考药物相当。