Berbamine 是一种从黄柏中提取的天然化合物,具有抗肿瘤、免疫调节和心血管作用。Berbamine是一种钙通道阻滞剂,并通过靶向 CaMKII 抑制肝癌生长。


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| 产品名称 | CaMKII ↓ ↑ | CaMKIII ↓ ↑ | CaMKKα ↓ ↑ | CaMKKβ ↓ ↑ | PKD ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| KN-62 |
+
CaMKII, Ki: 0.9 μM |
99% | |||||||||||||||||
| KN-93 |
++
CaMKII, Ki: 0.37 μM |
99% | |||||||||||||||||
| NH125 |
+++
eEF-2 kinase, IC50: 60 nM |
99%+ | |||||||||||||||||
| STO-609 |
++
CaM-KKα, Ki: 0.25 μM |
++++
CaM-KKβ, Ki: 47 nM |
98% | ||||||||||||||||
| CID755673 |
+++
PKD1, IC50: 180 nM PKD2, IC50: 227 nM |
99%+ | |||||||||||||||||
| CRT0066101 2HCl |
++++
PKD1, IC50: 1 nM PKD2, IC50: 2 nM |
99%+ | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Berbamine, a natural product isolated and purified from the roots of Cocculus orbiculatus (L.) DC., has high binding affinity toward the (GGA)8 G-quadruplex, and is a promising agent to suppress liver cancer growth by targeting CAMKII. |
| Concentration | Treated Time | Description | References | |
| PK-15 cells | 0.3-5 µM | 24 hours | Inhibited ASFV B646L gene transcription | J Virol. 2024 Aug 20;98(8):e0032724. |
| 3D4/21 cells | 0.4-6.4 µM | 24 hours | Inhibited ASFV B646L gene transcription | J Virol. 2024 Aug 20;98(8):e0032724. |
| Human intestinal epithelial monolayers | 36.7 μM | 5 days | To evaluate the inhibitory effect of Berbamine on SARS-CoV-2 pseudovirus entry into human intestinal epithelial monolayers. Results showed that Berbamine significantly inhibited SARS-CoV-2 pseudovirus entry. | Emerg Microbes Infect. 2023 Dec;12(1):2195020. |
| Caco-2 cells | 14.7, 7.3, 3.7 μM, or 1.8 μM | 72 hours | To evaluate the inhibitory effect of Berbamine on SARS-CoV-2 pseudovirus entry into Caco-2 cells. Results showed that Berbamine significantly inhibited SARS-CoV-2 pseudovirus entry. | Emerg Microbes Infect. 2023 Dec;12(1):2195020. |
| Porcine alveolar macrophages (PAMs) | 5 µM | 72 hours | Inhibited ASFV B646L gene transcription and p72 protein expression, completely suppressed virus titer | J Virol. 2024 Aug 20;98(8):e0032724. |
| Vero E6 cells | 0-200 μmol/L | 72 hours | Assess the inhibitory effect of berbamine hydrochloride on EBOV-EGFP and wild-type MARV infection, showing effective suppression of viral replication. | Acta Pharm Sin B. 2022 Dec;12(12):4378-4389. |
| HEK293T cells | 10 μmol/L | 48 hours | Evaluate the inhibitory effect of berbamine hydrochloride on EBOV pseudovirus infection, showing significant inhibition. | Acta Pharm Sin B. 2022 Dec;12(12):4378-4389. |
| BHK-21 cells | 15, 20 μM | 24 hours | To assess the inhibitory effect of Berbamine on cell fusion | iScience. 2024 Nov 8;27(12):111347. |
| Caco2 cells | 1.0 to 20 μM | To evaluate the antiviral activity of Berbamine against SARS-CoV-2 | iScience. 2024 Nov 8;27(12):111347. | |
| A549 cells | 1.0 to 20 μM | To evaluate the antiviral activity of Berbamine against SARS-CoV-2 | iScience. 2024 Nov 8;27(12):111347. | |
| Vero-E6 cells | 1.0 to 20 μM | To evaluate the antiviral activity of Berbamine against SARS-CoV-2 | iScience. 2024 Nov 8;27(12):111347. | |
| U87.LC3-mCherry-GFP cells | 73.4 μM | 24 hours | To evaluate the effect of Berbamine on autophagy flux. Results showed that Berbamine significantly inhibited autophagy flux. | Emerg Microbes Infect. 2023 Dec;12(1):2195020. |
| SMMC-7721 cells | 5 μM | 24 hours | BBM treatment resulted in accumulation of LC3B-II and SQSTM1, indicating autophagosome accumulation. | Cell Death Dis. 2018 Feb 14;9(2):243. |
| Eca109 cells | 5 μM | 24 hours | BBM treatment resulted in accumulation of LC3B-II and SQSTM1, indicating autophagosome accumulation. | Cell Death Dis. 2018 Feb 14;9(2):243. |
| A549 cells | 5 μM | 24 hours | BBM treatment resulted in accumulation of LC3B-II and SQSTM1, indicating autophagosome accumulation. | Cell Death Dis. 2018 Feb 14;9(2):243. |
| MDA-MB-231 cells | 5 μM | 24 hours | BBM treatment resulted in accumulation of LC3B-II and SQSTM1, indicating autophagosome accumulation. | Cell Death Dis. 2018 Feb 14;9(2):243. |
| MCF-7 cells | 5 μM | 24 hours | BBM treatment resulted in accumulation of LC3B-II and SQSTM1, indicating autophagosome accumulation. | Cell Death Dis. 2018 Feb 14;9(2):243. |
| Huh7 cells | 10 μM | 24 hours | Reduced ACE2 levels at the cell surface | Signal Transduct Target Ther. 2021 Apr 24;6(1):168. |
| HEK293T cells | 10 μM | Inhibited the entry of SARS-CoV-2 S pseudotyped particles into cells | Signal Transduct Target Ther. 2021 Apr 24;6(1):168. | |
| HeLa cells | 10 μM | 30 minutes | To evaluate the effect of Berbamine on intracellular calcium concentration. Results showed that Berbamine significantly inhibited GPN- or ML-SA1-induced lysosomal calcium release. | Emerg Microbes Infect. 2021 Dec;10(1):1257-1271. |
| A549 cells | 1.62 μM (EC50) | 48 hours | To evaluate the inhibitory effect of Berbamine on JEV infection. Results showed that Berbamine significantly inhibited JEV infection. | Emerg Microbes Infect. 2021 Dec;10(1):1257-1271. |
| 3D4/21 cells | 5 μM | 24 hours | To evaluate the inhibitory effect of berbamine hydrochloride on ASFV in 3D4/21 cells, results showed that berbamine hydrochloride significantly inhibited ASFV B646L gene transcription level. | Molecules. 2022 Dec 25;28(1):170. |
| PK-15 cells | 5 μM | 24 hours | To evaluate the inhibitory effect of berbamine hydrochloride on ASFV in PK-15 cells, results showed that berbamine hydrochloride significantly inhibited ASFV B646L gene transcription level. | Molecules. 2022 Dec 25;28(1):170. |
| Porcine alveolar macrophages (PAMs) | 0-5 μM | 24 hours | To evaluate the inhibitory effect of berbamine hydrochloride on African swine fever virus (ASFV) infection, results showed that berbamine hydrochloride inhibits ASFV in a dose-dependent manner. | Molecules. 2022 Dec 25;28(1):170. |
| Porcine alveolar macrophages (PAMs) | 50 µM | 24 hours | Evaluate the antiviral activity of Berbamine against ASFV Arm/07 strain, showing significant reduction in viral titer | Virol J. 2024 Apr 25;21(1):95. |
| Administration | Dosage | Frequency | Description | References | ||
| BALB/c mice | EBOV infection model | Oral | 100 mg/kg | Once daily for 6 days | Evaluate the protective effect of berbamine hydrochloride in EBOV-infected mice, showing significant improvement in survival rate. | Acta Pharm Sin B. 2022 Dec;12(12):4378-4389. |
| HACE2.Tg mice | SARS-CoV-2 infection model | Oral | 100 mg/kg body weight | 12 h before and immediately after infection, till 6 dpi | To evaluate the prophylactic effect of Berbamine against SARS-CoV-2 infection | iScience. 2024 Nov 8;27(12):111347. |
| BALB/c mice | JEV infection model | Intraperitoneal injection | 15 mg/kg | Twice daily for 14 days | To evaluate the protective effect of Berbamine on JEV-infected mice. Results showed that Berbamine significantly increased the survival rate (75% vs 12.5%) and alleviated brain damage. | Emerg Microbes Infect. 2021 Dec;10(1):1257-1271. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.64mL 0.33mL 0.16mL |
8.21mL 1.64mL 0.82mL |
16.43mL 3.29mL 1.64mL |
|
| CAS号 | 478-61-5 |
| 分子式 | C37H40N2O6 |
| 分子量 | 608.72 |
| SMILES Code | COC1=C(C2=C(C=C1OC)CCN([C@@]2(C3)[H])C)OC4=CC5=C(C=C4OC)CCN(C)[C@]([H])5CC(C=C6)=CC=C6OC7=CC3=CC=C7O |
| MDL No. | MFCD11501559 |
| 别名 | BA; BBM |
| 运输 | 蓝冰 |
| 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: 105 mg/mL(172.49 mM),配合低频超声助溶,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 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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