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 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
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。 |
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]. |
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 |
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 |
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 |
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 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
|