State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization and The Key Laboratory of Plant Resources and Chemistry of Arid Zone, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; University of the Chinese Academy of Sciences, Beijing 100039, China.
State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization and The Key Laboratory of Plant Resources and Chemistry of Arid Zone, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Chinese-Tajik Innovation Center of Natural Products of the National Academy Scinces of Tajikistan, Ainy St. 299/2, Dushanbe 734063, Tajikistan.
Fitoterapia. 2024 Jul;176:106035. doi: 10.1016/j.fitote.2024.106035. Epub 2024 May 25.
Six undescribed bicyclic sesquiterpene coumarins, kuhistanin A, ferukrin isovalerate, 9'β,12'α - ferukrin isovalerate, (17'E)- 9'α, 12'β - isomarcandin, (17'Z)- 9'α, 12'β - isomarcandin and (17'E) - isomarcandin, together with nine known ones were isolated from the roots of Ferula kuhistanica Korovin. The structures of them were elucidated using NMR and HRESIMS data analysis. The relative configurations of the isolates were confirmed by NOE correlations and NMR calculation. The absolute configurations of them were confirmed by X-ray diffraction analysis and ECD calculation. Anti-vitiligo, anti-inflammatory and cytotoxicity of the isolates were tested. Acetyl feselol, feselol, ferusingensine I and farnesiferol A significantly increased the melanin content at the concentration of 10 μM. (17'E) - 9'α, 12'β - isomarcandin exhibited strong cytotoxicity against HT-29 cell line with IC values of 8.94 ± 0.47 μM, and (17'E) - isomarcandin demonstrated strong cytotoxicity against Hela, A549 and HT-29 cell lines with IC values of 5.29 ± 0.25, 4.01 ± 0.20, and 4.16 ± 0.21 μM, respectively. This study concluded that, isolated compounds from F. kuhistanica demonstrated strong bioactivity towards anti-vitiligo and cytotoxicity and active compounds are suggested as anti-vitiligo and cytotoxicity agent for future drug development.
从 Ferula kuhistanica Korovin 的根部分离得到了六个未描述的双环倍半萜香豆素,分别为 kuhistanin A、ferukrin 异戊酸酯、9'β,12'α-ferukrin 异戊酸酯、(17'E)-9'α,12'β-isomarcandin、(17'Z)-9'α,12'β-isomarcandin 和 (17'E)-isomarcandin,以及另外九个已知化合物。它们的结构通过 NMR 和 HRESIMS 数据分析进行了阐明。通过 NOE 相关和 NMR 计算确定了它们的相对构型。通过 X 射线衍射分析和 ECD 计算确定了它们的绝对构型。对分离物进行了抗白癜风、抗炎和细胞毒性测试。乙酰 feselol、feselol、ferusingensine I 和 farnesiferol A 在 10 μM 浓度下显著增加黑色素含量。(17'E)-9'α,12'β-isomarcandin 对 HT-29 细胞系表现出强烈的细胞毒性,IC 值为 8.94±0.47 μM,而 (17'E)-isomarcandin 对 Hela、A549 和 HT-29 细胞系表现出强烈的细胞毒性,IC 值分别为 5.29±0.25、4.01±0.20 和 4.16±0.21 μM。本研究表明,从 F. kuhistanica 中分离得到的化合物具有很强的抗白癜风和细胞毒性活性,建议将活性化合物作为抗白癜风和细胞毒性药物,用于未来的药物开发。