Psoralidin(补骨脂定,补骨酯定)是一种从香豆素中提取出的天然产物,也是COX-2和5-LOX的双重抑制剂。Psoralidin不仅可以诱导ROS的生成,还能下调NOTCH信号通路,在转录上抑制Akt磷酸化和磷脂酰肌醇3激酶的激活。Psoralidin具有多种生物活性,如抗癌、抗炎、抗氧化、抗抑郁、胰岛素信号的调节等。Psoralidin还是雌激素受体(ER)α和ERβ的激动剂,IC50值分别为1.03 μM和24.6 μM。
参考文献
[1] Zhai Y, Li Y, et al. Psoralidin, a prenylated coumestan, as a novel anti-osteoporosis candidate to enhance bone formation of osteoblasts and decrease bone resorption of osteoclasts. Eur J Pharmacol. 2017 Apr 15; 801:62-71. doi: 10.1016/j.ejphar.2017.03.001. Epub 2017 Mar 8. PMID: 28283388.
[2] Rao Z, et al. Protective effects of psoralidin on IL‑1β‑induced chondrocyte apoptosis. Mol Med Rep. 2018 Feb;17(2):3418-3424. doi: 10.3892/mmr.2017.8248. Epub 2017 Dec 11. PMID: 29257269.
[3] Li J, et al. Psoralidin inhibits the proliferation of human liver cancer cells by triggering cell cycle arrest, apoptosis and autophagy and inhibits tumor growth in vivo. J BUON. 2019 Sep-Oct;24(5):1950-1955. PMID: 31786860.
[4] Xin Z, et al. Mechanisms explaining the efficacy of psoralidin in cancer and osteoporosis, a review. Pharmacol Res. 2019 Sep; 147:104334. doi: 10.1016/j.phrs.2019.104334. Epub 2019 Jun 28. PMID: 31255708.
[5] Zhang R, et al. Biological activity and health promoting effects of psoralidin. Pharmazie. 2019 Feb 1;74(2):67-72. doi: 10.1691/ph.2019.8619. PMID: 30782253.
冰袋运输。粉末直接保存于-20℃,有效期2年。建议分装后-20℃避光保存,避免反复冻融。