epiberberine是一种从黄连中提取的生物碱,作为 AChE 和 BChE 的有效抑制剂,同时也是 BACE1 的非竞争性抑制剂,具有抗氧化和抗阿尔茨海默症的作用,适用于神经退行性疾病和代谢疾病的研究。


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| Concentration | Treated Time | Description | References | |
| FaDu cells | 10, 20, 40 μM | 24 hours | To evaluate the effect of epiberberine on the migration and invasion of FaDu cells. Results showed that epiberberine significantly inhibited cell migration and invasion in a dose-dependent manner. | J Cell Mol Med. 2023 Dec;27(23):3796-3804 |
| Ca9-22 cells | 10, 20, 40 μM | 24 hours | To evaluate the effect of epiberberine on the migration and invasion of Ca9-22 cells. Results showed that epiberberine significantly inhibited cell migration and invasion in a dose-dependent manner. | J Cell Mol Med. 2023 Dec;27(23):3796-3804 |
| rat liver microsomes | 2.5, 5, 10, 20 μM | 120 minutes | Evaluate the inhibitory properties of EPI on CYP2D6, results showed that EPI had obvious noncompetitive inhibitory effects on CYP2D6 | Drug Des Devel Ther. 2017 Dec 28;12:57-65 |
| human liver microsomes | 2.5, 5, 10, 20 μM | 120 minutes | Evaluate the inhibitory properties of EPI on CYP2C9 and CYP2D6, results showed that EPI had obvious noncompetitive inhibitory effects on CYP2C9 and CYP2D6 | Drug Des Devel Ther. 2017 Dec 28;12:57-65 |
| Administration | Dosage | Frequency | Description | References | ||
| Sprague Dawley rats | Normal rats | Oral | 10, 54, 81 mg/kg | Single dose | Evaluate the pharmacokinetics and oral bioavailability of EPI in rats, results showed that EPI was rapidly absorbed and metabolized, with Tmax of 0.37–0.42 h, T1/2 of 0.49–2.73 h, and oral absolute bioavailability of 14.46% | Drug Des Devel Ther. 2017 Dec 28;12:57-65 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.97mL 0.59mL 0.30mL |
14.87mL 2.97mL 1.49mL |
29.73mL 5.95mL 2.97mL |
|
| CAS号 | 6873-09-2 |
| 分子式 | C20H18NO4 |
| 分子量 | 336.36 |
| SMILES Code | COC1=CC2=C(C3=[N+](CC2)C=C4C(OCO5)=C5C=CC4=C3)C=C1OC |
| MDL No. | MFCD01547982 |
| 别名 | |
| 运输 | 蓝冰 |
| InChI Key | FPJQGFLUORYYPE-UHFFFAOYSA-N |
| Pubchem ID | 160876 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 3 mg/mL(8.92 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
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