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Dauricine/蝙蝠葛碱 {[allProObj[0].p_purity_real_show]}

货号:A157527

Dauricine 是一种双苯异喹啉生物碱,具有抗炎活性。它通过抑制 NF-κB 激活,抑制结肠癌细胞的增殖和侵袭,并诱导细胞凋亡,且具剂量依赖性。

Dauricine/蝙蝠葛碱 化学结构 CAS号:524-17-4
Dauricine/蝙蝠葛碱 化学结构
CAS号:524-17-4
Dauricine/蝙蝠葛碱 3D分子结构
CAS号:524-17-4
Dauricine/蝙蝠葛碱 化学结构 CAS号:524-17-4
Dauricine/蝙蝠葛碱 3D分子结构 CAS号:524-17-4
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Dauricine/蝙蝠葛碱 纯度/质量文件 产品仅供科研

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产品名称 NF-κB 其他靶点 纯度
Ammonium pyrrolidine-1-carbodithioate 98%
QNZ ++++

NF-κB, IC50: 11 nM

99%+
Sodium 4-Aminosalicylate Dihydrate 98%
Sodium Salicylate 95%
Parthenolide p53 97% HPLC
JSH-23 +

NF-κB, IC50: 7.1 μM

98%
Phenethyl caffeate 98%
Andrographolide 98+%
Curcumin Nrf2,HDAC 98%
SC75741 +++

NF-κB, EC50: 200 nM

99%+
CBL0137 HCl ++

NF-κB, EC50: 0.47 μM

p53 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。

Dauricine/蝙蝠葛碱 生物活性

描述 Dauricine, a bisbenzylisoquinoline alkaloid derived from Menispermum dauricum, exhibits anti-inflammatory properties. It hampers cell proliferation and invasion and prompts apoptosis by inhibiting NF-κB activation in a dose- and time-dependent manner in colon cancer[1].
体内研究

Dauricine, when administered subcutaneously at 40 mg/kg every two days for nine days, inhibits the growth of colonic tumors in a HCT116 xenograft mouse model[1].

Dauricine, given intraperitoneally at 1 or 10 mg/kg, mitigates cognitive impairment, diminishes Aβ accumulation, and curtails Tau hyperphosphorylation in 3xTg-Alzheimer's Disease mice[2].

体外研究

Dauricine, at concentrations ranging from 0 to 20 μM over a period of 8 days, suppresses the growth of HCT116, HCT8, SW620, and SW480 cells[1].

Dauricine, at concentrations from 0 to 20 μM, induces G1 phase cell-cycle arrest in HCT116 cells after 12 and 24 hours of treatment[1].

Dauricine, in concentrations ranging from 0 to 20 μM over a period of 36 hours, induces apoptosis in HCT116 cells and inhibits their invasion[1].

Dauricine, administered at 0-20 μM for 6 hours, suppresses the activation of the NF-κB signaling pathway in HCT116 cells[1].

Dauricine (1 and 2 μg/mL, 24 h) inhibits glucose glycolysis and increased oxidative phosphorylation in HepG2 and Huh-7 cells[3].

Dauricine (2 μg/mL, 48 h) increases the sensitivities of HCC cell lines to both Cisplatin and Sorafenib[3].

Dauricine/蝙蝠葛碱 细胞实验

Cell Line
Concentration Treated Time Description References
A549 cells 5 and 15 µM 24 h To evaluate the effect of Dauricine on the proliferation of lung adenocarcinoma cells, results showed significant reduction in cell proliferation Cells. 2025 May 12;14(10):698
SH-SY5Y neuroblastoma cells 1 μM 24 h Evaluate the neuroprotective effects of DPM against Fe2+-induced toxicity, DPM significantly increased cell viability J Nanobiotechnology. 2020 Apr 19;18(1):61

Dauricine/蝙蝠葛碱 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice Subcutaneous cell line-derived syngeneic model Intraperitoneal injection 20 mg/kg Once daily for 21 days To evaluate the inhibitory effect of Dauricine on lung adenocarcinoma tumor growth in vivo, results showed significant inhibition of tumor growth Cells. 2025 May 12;14(10):698
Mice 3xTg-AD mouse model Intraperitoneal injection 1 or 10 mg/kg Once daily for 2 months DAU significantly improved cognitive impairments in 3xTg-AD mice by decreasing Aβ plaques and hyperphosphorylated tau and increasing the hippocampal ATP level. Front Cell Dev Biol. 2021 Feb 5;8:624339
C57BL/6 mice Autologous whole blood double infusion ICH model Tail vein injection 100 mg/kg DPM (equivalent to 10.1 mg/kg DRC) Administered immediately after ICH surgery, evaluated at 24 h Assess the improvement of DPM on neurological deficits, brain edema, and BBB permeability post-ICH, DPM significantly improved neurological scores, reduced brain water content and Evans blue leakage J Nanobiotechnology. 2020 Apr 19;18(1):61

Dauricine/蝙蝠葛碱 参考文献

[1]Yang Z, et al. Dauricine induces apoptosis, inhibits proliferation and invasion through inhibiting NF-kappaB signaling pathway in colon cancer cells. J Cell Physiol. 2010 Oct;225(1):266-75.

[2]Chen C, et al. Dauricine Attenuates Spatial Memory Impairment and Alzheimer-Like Pathologies by Enhancing Mitochondrial Function in a Mouse Model of Alzheimer's Disease. Front Cell Dev Biol. 2021 Feb 5;8:624339.

[3]Li W, et al. Dauricine upregulates the chemosensitivity of hepatocellular carcinoma cells: Role of repressing glycolysis via miR-199a:HK2/PKM2 modulation. Food Chem Toxicol. 2018 Nov;121:156-165.

Dauricine/蝙蝠葛碱 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.60mL

0.32mL

0.16mL

8.00mL

1.60mL

0.80mL

16.01mL

3.20mL

1.60mL

Dauricine/蝙蝠葛碱 技术信息

CAS号524-17-4
分子式C38H44N2O6
分子量 624.77
SMILES Code OC1=CC=C(C[C@H]2N(C)CCC3=C2C=C(OC)C(OC)=C3)C=C1OC4=CC=C(C[C@H]5N(C)CCC6=C5C=C(OC)C(OC)=C6)C=C4
MDL No. MFCD26960929
别名
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(168.06 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
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