Energize your cells, energize your body with MaxATP³™ , the first energy drink in the world powered by RiboCeine™ . Only MaxATP³ gives your body what it needs to produce sustained and consistent energy at the cellular level while also fighting against free radicals generated in the production of ATP.
Energy Beyond the Boost
Unlike other energy drinks that yield a short-term boost and little else, MaxATP³ provides a sustained source of energy by supporting the body's natural cellular production of ATP in three unique ways:
1. Fuels ATP production in the cells by providing the necessary nutrients, including optimal amounts of ribose.*
2. Replenishes energy and fights fatigue by helping your body convert food into energy. Optimal amounts of ATP help you feel less fatigued.*
3. Neutralizes free radicals. Only MaxATP³ can provide RiboCeine to assist your body in the production of glutathione, which helps to neutralize free radicals created during ATP production.*
Other energy drinks can't match these benefits because they can't match MaxATP³'s exclusive formulation. Even better, it's designed to work synergistically with MaxGXL® and Max N-Fuze™. All three can be taken together to give you unparalleled cellular protection, health and energy.Each box of MaxATP³ provides 15 convenient two-ounce bottles, and one bottle a day gives you a powerhouse of nutrients for unbeatable ATP support. When you want to energize your body, don't reach for a short-term boost. Reach instead for MaxATP³ and clean cellular energy.
MaxATP³ - The ultimate clean energy drink.
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.
What is ATP?
ATP, or adenosine triphosphate, is your body's most basic form of energy and is produced in every cell. It powers our cells, organs, and, by extension, our bodies. Many different components are required to produce ATP.
ATP in our bodies is like the battery in a car. Everything in the car is dependent on the energy from the battery. When the battery power runs low, the lights in the car begin to dim and the performance of the car starts to suffer. However, when the battery power is re-charged or restored, performance returns to normal and the car functions exactly how it was designed.
The Power of RiboCeine™
MaxATP³ does what other energy drinks can't because of RiboCeine, a breakthrough compound exclusive to Max International which provides key benefits tied to cellular energy.
First, it effectively protects and delivers the fragile cysteine molecule to the cell. Cysteine is often in limited supply in the body, but is an essential component needed for the production of glutathione, the body's master antioxidant. Glutathione is especially important due to its unique ability to protect the cell, where energy is created.
Second, RiboCeine also delivers ribose, a natural compound required for ATP, the basic form of cellular energy in the body.
MaxATP³ therefore delivers what your body needs to produce sustained and consistent energy at the cellular level while also fighting against free radicals generated in the production of ATP. MaxATP³ cleans up what others leave behind, supporting the optimal health of each and every cell.
Unlike all other energy drinks, MaxATP³ provides a comprehensive solution to the energy creation, support, and protection needs of your body.
FAQs
What is ATP?
A- ATP, or adenosine triphosphate, is your body’s most basic form of energy. ATP is produced in every cell and is the means by which our cells, organs, and by extension, our bodies are powered. ATP needs many different compounds or elements to be produced. MaxATP³ was designed with your body’s energy needs in mind and provides a comprehensive list of elements needed for ATP production which helps to provide a more sustained and consistent supply of cellular energy.
How is this energy drink different from others on the market?
A- MaxATP³ is focused more on providing your body with the elements it needs to produce sustained and consistent energy at the cellular level. Only MaxATP³ can provide RiboCeine™ which provides your body with the ribose it needs for ATP production and the cysteine it needs to support glutathione production to neutralize free radicals.
How does MaxATP³ support glutathione production in the body?
A- MaxATP³ features RiboCeine™, which effectively protects and delivers cysteine to the cell, enabling your body to produce glutathione more efficiently. Cysteine is a critical element needed to produce glutathione and is often in short supply in the body. Since it is broken down so easily during digestion, RiboCeine ensures that cysteine reaches the cell intact—available for glutathione production.
Can I take this energy drink with MaxGXL and Max N-Fuze?
A- MaxATP³ is designed to work synergistically with MaxGXL and Max N-Fuze and can be taken together.
Is this product based on the new science recently acquired by Max International?
A- Yes. MaxATP³ features RiboCeine™ a proprietary and patent-pending compound developed by Dr. Herbert Nagasawa after nearly 25 years of research.
What does the “3” in MaxATP³ stand for?
A- MaxATP³ supports your body’s energy needs in three (3) unique ways:
1- Fuels ATP production
2- Replenishes energy and fights fatigue
3- Neutralizes free radicals
What is a Flavonoid antioxidant?
A- Flavonoids are a large class of phytochemicals, also called polyphenols that are known to have health benefits due to their antioxidant activity. Anthocyanins, the pigments in colored fruits and vegetables are part of the flavonoid family.
What is an adaptogen?
A- Adaptogens are derived from herbs that are considered to increase the body’s ability to cope with stress, anxiety and fatigue. They are also considered to enhance performance and endurance.
Supporting Ingredients
Proprietary Blend:
Ribose - an essential component in the natural creation of ATP. Your body cannot create ATP without it.
N-acetyl -L-carnitine - increases the rate at which the liver oxidizes fat therefore increasing the amount of energy available. Carnitine shuttles long chain fatty acids from the liver into the mitochondria to be metabolized.
RiboCeine™ - an exclusive product comprised of ribose and cysteine, RiboCeine effectively passes through the digestive tract and delivers the fragile cysteine molecule to the cell, enabling efcient, natural production of glutathione. The ribose compound in RiboCeine is also used by the cell as an essential component to ATP production, your body’s source of energy. This allows your body to essentially manufacture glutathione “on demand” so it is ready to defend itself from free radical damage when it needs it most.
Panax Ginseng - Panax Ginseng is ginseng from Asia and is a known adaptogen to support an increased ow of steady energy throughout the day.
Green Tea Extract - is known to have high antioxidant activity and together with RiboCeine, promotes a critical step in the production of glutathione. It also provides the natural source of caffeine which acts as a natural metabolic enhancer and supports mental alertness.
Rhodiola Rosea - an adaptogen shown to reduce symptoms of fatigue and improve mental performance.
Quercetin - a avonoid antioxidant known to support energy levels.
CoQ10 - a powerful endogenous (made naturally in the body) antioxidant that resides in the mitochondria and is a vital component of the energy producing process of ATP. It helps to eliminate harmful free radicals produced during the ATP process.
Other Ingredients:
B Vitamins (thiamine, riboflavin, niacin, pantothenic acid, pyridoxine, biotin, folic acid, cyancobalamin) - support various enzymes that help convert food to energy. B Vitamins serve as coenzymes that assist in specific metabolic processes to break down fats, amino acids and carbohydrates for energy.
Magnesium - essential in all energy dependent reactions that include the use of ATP energy. It serves as a catalyst in the creation of ATP from ADP. It is also a catalyst when ATP is used for energy by helping in the hydrolysis of ATP (the act of releasing the energy stored in the high energy phosphate bond).
Copper - plays an important role supporting the synthesis of ATP in the mitochondria, or the part of the cell responsible for energy production.
Chromium - an essential trace element that is needed for the metabolism of energy. Chromium works with insulin and assists cells to uptake glucose and release energy.
Nutrition Facts
Directions for Use
Drink one two-ounce bottle daily as needed for increased energy. Store in a cool, dry place.
Guarantee/ Warning
This product has been manufactured in the USA in strict conformance with industry standards. Purity and potency guaranteed.
Warning: Keep out of the reach of children. This product is for adult use only. It is not intended for use by young children, pregnant women, or nursing mothers.
Roberts, J.C.; Nagasawa, H.T.; Zera, R.T.; Fricke, R.F.; Goon, D.J. W. Prodrugs of L-cysteine as protective agents against acetaminophen-induced hepatotoxicity. 2-(polyhydroxyalky)-and 2-(Polyacetoxyalky)-Thiazolidine-4(R)-Carboxylic Acids.
J. Med Chem. 1987, 30, 1891-1896. Roberts, J.C.; Francetic, D.J.; Zera, R.T. L-cysteine prodrug protects against cyclophosphamide urotoxicity without compromising therapeutic activity.
Cancer Chemotherapy and Pharmacology 1991, 28, 166-170. Roberts, J.C.; Francetic, D.J. Time course for the elevation of glutathione in numerous organs of L1210-bearing CDF1 mice given the L-cysteine prodrug, RibCys.
Toxicology Letters, 1991, 59, 245-251. Roberts, J.C.; Francetic, D.J. Mechanisms of Chemoprotection by RibCys, a Thiazolidine Prodrug of L-cysteine.
Med. Chem. Res., 1991, 1, 213-219. Roberts, J.C.; Charyulu, R. L.; Zera, R.T.; Nagasawa, H.T. Protection Against Acetaminophen Hepatotoxicity by Ribose-Cysteine (RibCys).
Pharmacology & Toxicology, 1992, 70, 281-285. Rowe, J.K.; Zera, R.T.; Madoff, R.D.; Fink, A.S.; Roberts, J.C.; Johnston, G.R.; Freeney, D.A.;Young, H.L.; Bubrick, M.P. Protective Effect of RibCys Following High-Dose Irradiation of the Rectosigmoid.
Dis. Colon Rectum, 1993, 36(7), 681-687. Roberts, J.C.;Francetic, D.J.; Zera, R.T. Chemoprotection against Cyclophosphamide-Induced Urotoxicity: Comparison of Nine Thiol Protective Agents. AntiCancer Research, 1994, 14, 389-396.
Carroll, M.P.; Zera, R.T.; Roberts, J.C.; Schlafmann, S.E.; Feeny, D.A.; Johnston, G.R.; West, M.A.; Bubrick, M.P. Efficacy of Radioprotective Agents in Preventing Small and Large Bowel Radiation Injury.
Dis. Colon Rectum, 1995, 38(7), 716-722. Roberts, J.C.; Koch, K.E.; Detrick, S.R.; Warters, R.L.; Lubec G. Thiazolidine Prodrugs of Cysteamine and Cysteine as Radioprotective Agents.
Radiation Research, 1995, 143, 203-213. Bantseev, V.; Bhardwaj, R.; Rathbun, W.; Nagasawa, H.T.; Trevithick, J.R. Antioxidants and Cataract: (Cataract Induction in Space Environment and Application to Terrestrial Aging Cataract).
Biochem. Mol. Bio. Intl., 1997, 42, 1189-1197. Roberts, J.C.; Phaneuf, H.L.; Szakacs, J.G.; Zera, R.T.; Lamb, J.G.; Franklin, M.R. Differential Chemoprotection against Acetaminophen-Induced Hepatotoxicity by Latentiated L-Cysteines.
Chem. Res. Toxicol., 1998, 11, 1274-1282. Roberts, J.C.; Phaneuf, H.L.; Dominick, P.K.; Wilmore, B.H.; Cassidy, P.B. Biodistribution of [35S] - Cysteine and Cysteine Prodrugs: Potential Impact on Chemoprotection Strategies.
J. Labelled Cpd. Radiopharm., 1999, 42, 485-495. Lucus, A.M.; Henning G.; Dominick, P.K.; Whiteley, H.E.; Roberts, J.C.; Cohen, S.D. Ribose Cysteine Protects Against Acetaminophen-Induced Hepatic and Renal Toxicity.
Toxicologic Pathology, 2000, 28(5), 697-704. Wilmore, B.H.; Cassidy, P.B.; Warters, R.L.; Roberts, J.C. Thiazolidine Prodrugs as Protective Agents against y-Radiation-Induced Toxicity and Mutagenesis in V79 Cells.
J. Med. Chem., 2001, 44(16), 2661-2666. Lenarczyk, M.; Ueno, A.; Vannais, D.B.; Kraemer, S.; Kronenberg, A.; Roberts, J.C.; Tatsumi, K.; Hei, T.K.; Waldren, C.A. The "Pro-drug" RibCys Decreases the Mutagenicity of High-LET Radiation in Cultured Mammalian Cells.
Radiation Research, 2003, 160, 579-583. Lucas Slitt, A.M.; Dominick, P.K.; Roberts, J.C.; Cohen, S.D. Effect of Ribose Cysteine Pretreatment on Hepatic and Renal Acetaminophen Metabolite Formation and Glutathione Depletion.
Basic Clin. Pharmacol. Toxicol., 2005, 96 (6), 487-94. Oz, H.S.; Chen, T.S.; Nagasawa, H., Comparative efficacies of 2 cysteine prodrugs and a glutathione delivery agent in a colitis model.
Translational Research, 2007, 150(2), 122-129. Scientific Studies
Fu Y, Zheng S, Lu SC, Chen A. Epigallocatechin-3-gallate Inhibits Growth of Activated Hepatic Stellate Cells by Enhancing the Capacity of Glutathione Synthesis. Mol Pharmacol. 2008;73(5):1465-1473.
Sharma RA, Ireson CR, Verschoyle RD, Hill KA, Williams ML, Leuratti C, Manson MM, Marnett LJ, Steward WP, Gescher A. Effects of Dietary Curcumin on Glutathione S-Transferase and Malondialdehyde-DNA Adducts in Rat Liver and Colon Mucosa: Relationship with Drug Levels. Clinical Cancer Research. 2001;7(5):1452-1458.
Fahey JW, Talalay P. Antioxidant Functions of Sulforaphane: a Potent Inducer of Phase II Detoxication Enzymes. Food and Chemical Toxicology. 1999;(37):973-979.
Riedl MA, Saxon A, Diaz-Sanchez D. Oral sulforaphane increases Phase II antioxidant enzymes in the human upper airway. Clinical Immunology. 2009;(130):244-251.
Gasper AV, Al-janobi A, Smith JA, Bacon JR, Fortun P, Atherton C, Taylor MA, Hawkey CJ, Barrett DA, Mithen R. Glutathione S-transferase M1 polymorphism and metabolism of sulforaphane from standard and high-glucosinolate broccoli. Am J Clin Nutr. 2005;(82):1283-91.
Morimitsu Y, Nakagawa Y, Hayashi K, Fujii H, Kumagai T, Nakamura Y, Osawa T, Horio F, Itoh K, Iida K, Yamamoto M, Uchida K. A Sulforaphane Analogue That Potently Activates the Nrf2-dependent Detoxication Pathway. The Journal of Biological Chemistry. 2002;277(5):3456-3463.