Urolithin A 8-Methyl Ether Description
- What is Urolithin A 8-Methyl Ether ?
Urolithin A 8-Methyl Ether is easily soluble in N, N-dimethylformamide, dimethylsulfoxide, and slightly soluble in methanol, ethanol and ethyl acetate. It is the product after the hydrogen atom in the 8th hydroxyl of urolithin A is replaced by methyl. It has similar pharmacological effect with urolithin a, with anti-inflammatory and antioxidant effects, and its chemical properties are more stable than urolithin a due to methyl substitution.
- Urolithin A 8-Methyl Etheruses
Urolithin A 8-Methyl Ether is an intermediate in the synthesis of Urolithin A, a major metabolite of Ellagitannin. Which is used to anti-inflammatory and antioxidant.
- Urolithin A 8-Methyl Etherbenefits
Urolithin A 8-Methyl Ether is an intermediate in the synthesis of Urolithin A (U847000), a major metabolite of Ellagitannin and exhibits anti-inflammatory and antioxidant properties. It can improve mitochondrial and muscle function and improves muscle strength and endurance during aging.
- Urolithin A 8-Methyl Etherdosage
The appropriate dose of Urolithin A 8-Methyl Ether depends on several factors such as the user’s age, health, and several other conditions. At this time there is not enough scientific information to determine an appropriate range of doses for Urolithin A 8-Methyl Ethers. Keep in mind that natural products are not always necessarily safe and dosages can be important. Be sure to follow relevant directions on product labels and consult your pharmacist or physician or other healthcare professional before using.
- Urolithin A 8-Methyl Etherfor sale (Where to Buy Urolithin A 8-Methyl Ether)
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Urolithin A 8-Methyl Ether Specifications
|Name:||Urolithin A 8-Methyl Ether|
|Molecular Weight:||242.23 g/mol|
|Function:||Improve mitochondrial and muscle function and improves muscle strength and endurance during aging.|
|Application:||Used for anti-inflammatory and antioxidant.|
|Solubility:||Easily soluble in N, N-dimethylformamide, dimethylsulfoxide, and slightly soluble in methanol, ethanol and ethyl acetate.|
|Storage Temp:||Hygroscopic, -20°C Freezer, Under inert atmosphere|
|Shipping Condition:||Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.|
. Kasimsetty, S. G., et al.: J. Agri. Food. Chem., 58, 2180 (2010); Bialonska, D., et al.: J. Agri. Food. Chem., 57, 10181 (2009)
. M. Dell’Agli, G. V. Galli, M. Bulgari et al., “Ellagitannins of the fruit rind of pomegranate (Punica granatum) antagonize in vitro the host inflammatory response mechanisms involved in the onset of malaria,” Malaria Journal, vol. 9, no. 1, article 208, 2010.
. A. González-Sarrías, M. Larrosa, F. A. Toms-Barberán, P. Dolara, and J. C. Espín, “NF-κB-dependent anti-inflammatory activity of urolithins, gut microbiota ellagic acid-derived metabolites, in human colonic fibroblasts,” British Journal of Nutrition, vol. 104, no. 4, pp. 503–512, 2010.
. J. A. Giménez-Bastida, A. González-Sarrías, M. Larrosa et al., “Ellagitannin metabolites, urolithin A glucuronide and its aglycone urolithin A, ameliorate TNF-α induced inflammation and associated molecular markers in human aortic endothelial cells,” Molecular Nutrition & Food Research, vol. 56, no. 5, pp. 784–796, 2012.
. S. G. Kasimsetty, D. Bialonska, M. K. Reddy, C. Thornton, K. L. Willett, and D. Ferreira, “Effects of pomegranate chemical constituents/intestinal microbial metabolites on CYP1B1 in 22Rv1 prostate cancer cells,” Journal of Agricultural and Food Chemistry, vol. 57, no. 22, pp. 10636–10644, 2009.