Rubusoside是一种天然甜味剂和溶解剂,具有抗血管生成、抗癌、抗过敏等作用,并能减轻气道炎症、抑制脂毒性,广泛应用于呼吸道疾病及代谢相关疾病的研究。
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描述 | Rubusoside is a natural sweetener and a solubilizing agent with antiangiogenic and antiallergic properties. |
Concentration | Treated Time | Description | References | |
GLUT1 | 20 mM | 1 minute | Rub inhibits GLUT1-mediated glucose transport with an IC50 of 4.6 ± 0.3 mM. | Sci Rep. 2015 Aug 26;5:12804 |
GLUT5 | 20 mM | 1 minute | Rub inhibits GLUT5-mediated fructose transport with an IC50 of 6.7 ± 0.2 mM. | Sci Rep. 2015 Aug 26;5:12804 |
MCF-7 cells | 23 µM CUR and 110 µM RES | 24 hours | To evaluate the anti-cancer effect of RUB/CUR + RES micelles on MCF-7 cells, results showed that RUB/CUR + RES micelles had more significant toxicity on MCF-7 cells compared to RUB/CUR micelles + RUB/RES micelles. | Nanoscale Res Lett. 2017 Dec;12(1):274 |
Streptococcus mutans ATCC25175 | 1% | 5 days | To evaluate the effect of Rubusoside on Streptococcus mutans biofilm formation and virulence gene expression. Results showed that Rubusoside significantly reduced biofilm accumulation, bacterial viability, and polysaccharide production, and inhibited virulence gene expression. | Appl Environ Microbiol. 2020 Aug 3;86(16):e01012-20 |
Administration | Dosage | Frequency | Description | References | ||
Nude mice | OVCAR-3 or A2780 xenograft tumor model | Intraperitoneal injection | 1 mg/kg | Once every 3 days for 24 days | To evaluate the effect of Cer-RUB nanomicelles on tumor growth, results showed that Cer-RUB nanomicelles significantly inhibited the growth of OVCAR-3 tumors | Mol Cancer Ther. 2020 Feb;19(2):564-574 |
Sprague Dawley rats | Pre-cannulated rat model | Oral gavage and intravenous injection | Oral 20 mg/kg, intravenous 2 mg/kg | Single dose, observed for 24 hours | Compare pharmacokinetic parameters of Nano-PTX and Taxol? formulations in rat model, results showed oral bioavailability of Nano-PTX formulation was 1.7%, 88% higher than Taxol? formulation (1.3%) | Pharmaceutics. 2024 Aug 22;16(8):1104 |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.56mL 0.31mL 0.16mL |
7.78mL 1.56mL 0.78mL |
15.56mL 3.11mL 1.56mL |
CAS号 | 64849-39-4 |
分子式 | C32H50O13 |
分子量 | 642.73 |
SMILES Code | O=C(C1(C)C2CCC(CC([C@]3(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)CC5)=C)(C3)[C@]5([H])[C@]2(C)CCC1)O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6 |
MDL No. | MFCD06799426 |
别名 | 甜叶悬钩子苷 |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
溶解方案 |
DMSO: 105 mg/mL(163.37 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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