S-Acetyl Glutathione 60 C by Xymogen

S-Acetyl Glutathione

Xymogen

$71.99
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SKU:
XY-SAG-1
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S-Acetyl Glutathione by Xymogen

S-Acetyl Glutathione by Xymogen is a detox supplement designed with a specialized acetylated variant of glutathione for the best absorption.* As such, it may stand out among similar products due to its efficacy—it’s a product you may want to consider.*

Who May Take S-Acetyl Glutathione by Xymogen?

S-Acetyl Glutathione may be for you if:

  • you smoke cigarettes or drink a lot of alcohol*
  • you live in highly polluted areas*
  • you’re over 40*
  • you want to support your immune response*

S-Acetyl Glutathione by Xymogen—Potential Health Benefits

S-Acetyl Glutathione by Xymogen may support:

  • anti-oxidation*
  • cell function and healthy aging*
  • detoxification*
  • immune response*
  • amino acid transport across cell membranes*

Supplements support your health but do not replace a balanced diet. Always check with your healthcare practitioner if you have doubts about a new supplement. Book a FREE product consultation to learn more about this supplement.

Recommendation:
Xymogen suggests taking one to two capsules 1 to 2 times a day, or as recommended by your healthcare professional.

Serving Size: 2 capsules
Servings Per Container: 30 or 60

Amount Per Serving:
S-Acetyl Glutathione 200 mg

Other Ingredients: Acid-resistant capsule (hypromellose, gellan gum, and water), microcrystalline cellulose, stearic acid, magnesium stearate, and silica.

Does Not Contain: Wheat, gluten, corn, yeast, soy, animal and dairy products, fish, shellfish, peanuts, tree nuts, egg, sesame, ingredients derived from genetically modified organisms (GMOs), artificial colors, artificial sweeteners, and artificial preservatives.

Caution: Consult your healthcare professional prior to use. Individuals taking medication should discuss potential interactions with their healthcare professional. Do not use if tamper seal is damaged.

Storage: Keep closed in a cool, dry place out of reach of children.

Click here to view Data Sheet

LEGAL NOTICE: Xymogen's Exclusive Professional Formulas are available through select licensed health care professionals. The Internet Sale and Discounting of XYMOGEN formulas are strictly prohibited. covenanthealthproducts.com makes XYMOGEN formulas available only to patients of our clinic. If you are a patient of covenanthealthproducts.com, you may inquire about XYMOGEN by calling (800) 627-6518

References:

  1. Locigno, R., Pincemail, J., Henno, A., et al. (2002). S-Acetyl-glutathione selectively induces apoptosis in human lymphoma cells through a GSH-independent mechanism. International Journal of Oncology, 20(1), 69–75. https://doi.org/10.3892/ijo.20.1.69
  2. Lomaestro, B. M., & Malone, M. (1995). Glutathione in health and disease: Pharmacotherapeutic issues. Annals of Pharmacotherapy, 29(12), 1263–1273. https://doi.org/10.1177/106002809502901205
  3. Cacciatore, I., Cornacchia, C., Pinnen, F., et al. (2010). Prodrug approach for increasing cellular glutathione levels. Molecules, 15(3), 1242–1264. https://doi.org/10.3390/molecules15031242
  4. Vogel, J., Cinatl, J., Dauletbaev, N., et al. (2005). Effects of S-acetylglutathione in cell and animal models of herpes simplex virus type 1 infection. Medical Microbiology and Immunology, 194(1–2), 55–59. https://doi.org/10.1007/s00430-003-0215-2
  5. Ballatori, N., Krance, S. M., Notenboom, S., et al. (2009). Glutathione dysregulation and the etiology and progression of human diseases. Biological Chemistry, 390(3), 191–214. https://doi.org/10.1515/BC.2009.033
  6. Richman, P. G., & Meister, A. (1975). Regulation of gamma-glutamyl-cysteine synthetase by nonallosteric feedback inhibition by glutathione. Journal of Biological Chemistry, 250(4), 1422–1426. https://doi.org/10.1016/S0021-9258(19)41799-5
  7. Anderson, M. E., Powrie, F., Puri, R. N., et al. (1985). Glutathione monoethyl ester: Preparation, uptake by tissues, and conversion to glutathione. Archives of Biochemistry and Biophysics, 239(2), 538–548. https://doi.org/10.1016/0003-9861(85)90289-6
  8. Anderson, M. E., Nilsson, M., & Sims, N. R. (2004). Glutathione monoethyl ester prevents mitochondrial glutathione depletion during focal cerebral ischemia. Neurochemistry International, 44(3), 153–159. https://doi.org/10.1016/j.neuint.2003.08.002
  9. Kretzschmar, M. (1996). Regulation of hepatic glutathione metabolism and its role in hepatotoxicity. Experimental and Toxicologic Pathology, 48(5), 439–446. https://doi.org/10.1016/S0940-2993(96)80073-6
  10. Fraternale, A., Paoletti, M. F., Casabianca, A., et al. (2006). Antiviral and immunomodulatory properties of new pro-glutathione (GSH) molecules. Current Medicinal Chemistry, 13(15), 1749–1755. https://doi.org/10.2174/092986706777935185
  11. Kretzschmar, M., & Klinger, W. (1990). The hepatic glutathione system—influences of xenobiotics. Experimental Pathology, 38(3), 145–164. https://doi.org/10.1016/S0940-2993(11)80031-3
  12. Donnerstag, B., Ohlenschlager, G., Cinatl, J., et al. (1996). Reduced glutathione and S-acetylglutathione as selective apoptosis-inducing agents in cancer therapy. Cancer Letters, 110(1–2), 63–70. https://doi.org/10.1016/S0304-3835(96)04474-9