中文名 | 防己诺林碱 |
英文名 | Fangchinoline |
中文别名 | 汉防己乙素 |
英文别名 | Hanfangchin B; 12-O-Methylatherospermoline; Menisidine |
来源 | 粉防己Stephania tetrandra S. Moore |
化合物类型 | 生物碱(Alkaloids)>异喹啉生物碱>双苄基异喹啉生物碱 |
化学式 | C37H40N2O6 |
分子量 | 608.72 |
CAS号 | 436-77-1 |
纯度 | 98%, HPLC |
溶剂/溶解度 | DMSO: 50 mg/ml (82.14 mM) |
溶液配制 | 10mg加入1.64ml DMSO,或者每6.09mg加入1ml DMSO,配制成10mM溶液。 |
产品描述 | Fangchinoline is isolated from Stephania tetrandra with extensive biological activities, such as enhancing immunity, anti-inflammatory sterilization and anti-atherosclerosis. Fangchinoline, a novel HIV-1 inhibitor, inhibits HIV-1 replication by impairing gp160 proteolytic processing. Fangchinoline targets Focal adhesion kinase (FAK) and suppresses FAK-mediated signaling pathway in tumor cells which highly expressed FAK. Fangchinoline induces apoptosis and adaptive autophagy in bladder cancer. | ||||
信号通路 | HIV-1; Apoptosis; Autophagy | ||||
靶点 | Focal adhesion kinase (FAK) | - | - | - | - |
IC50 | - | - | - | - | - |
体外研究 | Fangchinoline (2.5-40 µM; 24-96 hours) inhibits both T24 and 5637 cells in dose-dependent manner, the IC50 values of Fangchinoline in T24 cells are 19.0 µM (24 h), 12.0 µM (48 h) and 7.57 µM (72 h), and 11.9 µM (24 h), 9.92 µM (48 h) and 7.13 µM (72 h) in 5637 cells. Fangchinoline (5 µM; 24 hours) induces a significant increase in the LC3-II/LC3-I ratio and a decrease in p62 in both T24 and 5637 cells, and causes a significant increase in the cleavage of caspase-3. | ||||
体内研究 | N/A | ||||
临床实验 | N/A |
1.Wan Z, et al. PLoS One. 2012,7(6):e39225.
2.Guo B, et al. J Drug Target. 2015,23(3):266-74.
3.Fan B, et al. Cell Physiol Biochem. 2017,43(3):1003-1011.
包装清单:产品编号 | 产品名称 | 包装 |
SM4116-10mM | 防己诺林碱(98%, HPLC) | 10mM×0.2ml |
SM4116-25mg | 防己诺林碱(98%, HPLC) | 25mg |
SM4116-100mg | 防己诺林碱(98%, HPLC) | 100mg |
- | 说明书 | 1份 |
-20℃避光保存,至少一年有效。固体粉末4℃避光保存,至少一个月有效。如果溶于非DMSO溶剂,建议分装后-80℃避光保存,预计6个月内有效。
注意事项:本产品可能对人体有一定的毒害作用,请注意适当防护,以避免直接接触人体或吸入体内。
本产品仅限于专业人员的科学研究用,不得用于临床诊断或治疗,不得用于食品或药品,不得存放于普通住宅内。
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