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Chemical Structure| 603-61-2 Chemical Structure| 603-61-2

Structure of Tamarixetin
CAS No.: 603-61-2

Chemical Structure| 603-61-2

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Tamarixetin (4'-O-Methyl Quercetin) is a natural flavonoid derivative of quercetin with antioxidant and anti-inflammatory properties. Tamarixetin prevents myocardial hypertrophy.

Synonyms: 4'-O-Methyl Quercetin; 4'-methoxy Quercetin

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Product Details of Tamarixetin

CAS No. :603-61-2
Formula : C16H12O7
M.W : 316.26
SMILES Code : O=C1C(O)=C(C2=CC=C(OC)C(O)=C2)OC3=CC(O)=CC(O)=C13
Synonyms :
4'-O-Methyl Quercetin; 4'-methoxy Quercetin
MDL No. :MFCD00017308

Safety of Tamarixetin

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
MCF-7 50 µM 48 hours Inhibition of cell proliferation, inhibition rate of 92.70% Sci Rep. 2022 Mar 10;12(1):3966
NRK-52E cells 12.5 µM 24 hours Tamarixetin did not show significant cytoprotective effects in NRK-52E cells. Molecules. 2022 Feb 15;27(4):1319
HK-2 cells 12.5 µM 24 hours Tamarixetin showed a cytoprotective trend in HK-2 cells, but the results were not significant. Molecules. 2022 Feb 15;27(4):1319
T47D 100 µM 48 hours Inhibition of cell proliferation, inhibition rate of 86.68% Sci Rep. 2022 Mar 10;12(1):3966
MDA-MB-453 50 µM 48 hours Inhibition of cell proliferation, inhibition rate of 44.97% Sci Rep. 2022 Mar 10;12(1):3966
MDA-MB-468 50 µM 48 hours Inhibition of cell proliferation, inhibition rate of 88.14% Sci Rep. 2022 Mar 10;12(1):3966
MDA-MB-231 50 µM 48 hours Inhibition of cell proliferation, inhibition rate of 71.02% Sci Rep. 2022 Mar 10;12(1):3966
Primary breast cancer cells 50 µM 48 hours Inhibition of cell proliferation, inhibition rate of 87.20% Sci Rep. 2022 Mar 10;12(1):3966
Chondrocytes differentiated from human bone-marrow-derived mesenchymal stem cells (hBMMSCs) 2, 5, 10, 20 µM 48 hours To evaluate the effects of Tamarixetin on chondrocyte viability and chondrogenic properties. Results showed that Tamarixetin did not induce observable cytotoxicity and significantly increased glycosaminoglycan (GAG) content and the expression of chondrogenic markers (COL2, ACAN, and SOX9). Antioxidants (Basel). 2024 Sep 25;13(10):1166

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.16mL

0.63mL

0.32mL

15.81mL

3.16mL

1.58mL

31.62mL

6.32mL

3.16mL

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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