Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, 35516 Mansoura, Egypt; National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS 38677, USA.
National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS 38677, USA.
Fitoterapia. 2024 Sep;177:106106. doi: 10.1016/j.fitote.2024.106106. Epub 2024 Jun 28.
The Cichorium plants are particularly notable due to their remarkable therapeutic and medicinal properties, besides being used as food and conventional medication. Although Cichorium plants have been studied for their phytoconstituents and biological activities, there is limited knowledge about the constituents of the roots of C. bottae. A phytochemical study of the 90% MeOH extract of C. bottae roots resulted in the isolation of twelve compounds belonging to guaianolide sesquiterpene lactones, sesquiterpene lactone glucosides, and phenolic derivatives, of which two compounds designated as 9α-hydroxycrepediaside B (1) and cichobotinal (2) were previously undescribed. The isolated compounds were assessed for their anti-inflammatory potential through the inhibition of inducible nitric oxide synthase (iNOS) and resultant decrease in nitric oxide generation in LPS-induced macrophages. Among the isolates, compounds 2 and 11 (8-deoxylactucin) inhibited iNOS activity with IC values of 21.0 ± 4 and 6.8 ± 0.1 μM, respectively. The methanolic extract of C. bottae inhibited iNOS with an IC of 10.5 ± 0.5 μg/mL.
菊苣属植物不仅可作为食物和传统药物使用,还具有显著的治疗和药用特性,因此尤为引人注目。虽然已经对菊苣属植物的植物成分和生物活性进行了研究,但对于菊苣属植物的根的成分知之甚少。对菊苣属植物根的 90%甲醇提取物进行了植物化学研究,结果分离得到了 12 种化合物,它们属于愈创木烷型倍半萜内酯、倍半萜内酯糖苷和酚类衍生物,其中两种化合物被命名为 9α-羟基克劳迪苷 B(1)和菊苣醇(2),它们以前未被描述过。通过抑制诱导型一氧化氮合酶(iNOS)和 LPS 诱导的巨噬细胞中一氧化氮的产生,评估了分离得到的化合物的抗炎潜力。在分离得到的化合物中,化合物 2 和 11(8-去氧乳清酸)对 iNOS 活性的抑制作用分别为 21.0 ± 4 和 6.8 ± 0.1 μM,IC 值。菊苣属植物的甲醇提取物对 iNOS 的抑制作用 IC 为 10.5 ± 0.5 μg/mL。