生物活性 | |||
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描述 | Chelidonine is a benzophenanthridine alkaloid isolated from Chelidonium majus L.. Chelidonine potently induced apoptosis of Jurkat A3 T-lymphoma cells within 24 hours at a concentration of 1μM[3]. HepG2 cells also showed apoptotic features after 24 hours of chelidonine treatment (LD50 = 12μM)[4]. In human glioblastoma T98G cells, treatment with chelidonine at 0.2–1.0μM induced G2/M arrest and increased the sub-G1/0 population size in a concentration-dependent manner[5]. Chelidonine at a non-cytotoxic dose (5mg/kg) enhanced the antitumor effect of lenvatinib on the intrahepatic growth of hepatocellular carcinoma MHCC97-H cells in nude mice[6]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.83mL 0.57mL 0.28mL |
14.15mL 2.83mL 1.41mL |
28.30mL 5.66mL 2.83mL |
参考文献 |
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