Ambeed.cn

首页 / / / / Berbamine/小檗胺

Berbamine/小檗胺 {[allProObj[0].p_purity_real_show]}

货号:A145417 同义名: BA; BBM

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。

Berbamine/小檗胺 化学结构 CAS号:478-61-5
Berbamine/小檗胺 化学结构
CAS号:478-61-5
Berbamine/小檗胺 3D分子结构
CAS号:478-61-5
Berbamine/小檗胺 化学结构 CAS号:478-61-5
Berbamine/小檗胺 3D分子结构 CAS号:478-61-5
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} 现货 1周 咨询 - +
购物车0 收藏 询单

Berbamine/小檗胺 纯度/质量文件 产品仅供科研

货号:A145417 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

全球学术期刊中引用的产品

Nature, 2025, 645, 793-800. Ambeed. [ A201204 , A444152 , A344107 , A952055 ]
Cell, 2025. Ambeed. [ A122167 ]
Science, 2025, 387(6729): eadp5637. Ambeed. [ A875019 ]
Sig. Transduct. Target. Ther., 2025, 10, 257. Ambeed. [ A104916 ]
Nat. Nanotechnol., 2025. Ambeed. [ A243018 , A1216705 , A522597 , A125401 , A1355641 ]
更多 >
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。

Berbamine/小檗胺 生物活性

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.

Berbamine/小檗胺 细胞实验

Cell Line
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.

Berbamine/小檗胺 动物实验

Species
Animal Model
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.

Berbamine/小檗胺 参考文献

[1]Parhi P, Suklabaidya S, et al. Enhanced anti-metastatic and anti-tumorigenic efficacy of Berbamine loaded lipid nanoparticles in vivo. Sci Rep. 2017 Jul 19;7(1):5806.

[2]Zhao Y, Lv JJ, et al. Berbamine inhibited the growth of prostate cancer cells in vivo and in vitro via triggering intrinsic pathway of apoptosis. Prostate Cancer Prostatic Dis. 2016 Dec;19(4):358-366.

Berbamine/小檗胺 实验方案

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

Berbamine/小檗胺 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
方案 二
AmBeed 相关网站 AmBeed.cn AmBeed.com
AmBeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    AmBeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。