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Chemical Structure| 64849-39-4 Chemical Structure| 64849-39-4

Structure of Rubusoside
CAS No.: 64849-39-4

Chemical Structure| 64849-39-4

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Rubusoside is a natural sweetener and a solubilizing agent with antiangiogenic and antiallergic properties.

Synonyms: Rubusoside

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Product Details of Rubusoside

CAS No. :64849-39-4
Formula : C32H50O13
M.W : 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
Synonyms :
Rubusoside
MDL No. :MFCD06799426

Safety of Rubusoside

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
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

In Vivo:

Species
Animal Model
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

Protocol

Bio Calculators
Preparing Stock Solutions 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

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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