A NEW ADIPO-X®? WHY IMPROVE ON PERFECTION?
ADIPO-X®, our original, best-selling
Fat Incinerator, was specifically formulated to attack fat more aggressively
than old school ephedrine. And it did. Powerful and strong,
ADIPO-X® worked like no other product on the market before it.
ADIPO-X® original contains potent
thermogenic components and effective metabolic up-regulators in addition
to several key fat mobilizing and appetite-suppressing agents. The original
ADIPO-X® formulation is a very formidable weapon
in the war on fat. So why did we even think about changing
it?
YOU ASKED FOR IT, SO WE DID IT!
The original ADIPO-X® has been
so successful for us we were surprised when a few of you asked for
more...
For those of you who want the push over
the cliff, the final word in fat loss, we, made a few subtle but significant
changes that make ADIPO-X® Version 2.0 even better than its powerful
predecessor.
SIMPLY STRONGER THAN BIG BROTHER...
ATTACK FAT FROM ALL ANGLES! Like it's older brother, this next generation formula utilizes multiple
metabolic pathways to target fat loss, allowing the body to maintain
continuous, increased and ongoing fat-burning and coaxing the body to
use fat first for fuel while sparing the breakdown of precious
muscle tissue.
ADIPO-X®
v2.0's clinically proven ingredients ramp up fat loss by stimulating
the body's primary fat-mobilizing hormones, epinephrine and norepinephrine,
to mobilize fatty acids from storage to be used for energy.
ADIPO-X®
v2.0 clinically-proven, multi-pronged attack on fat works in the
following ways:
1. Stimulates increased release
of epinephrine and norepinephrine, the body's primary fat loss
hormones. Epinephrine and norepinephrine stimulate the beta adrenergic
receptors of the fat cell, or adipocyte, triggering the mobilization
of fatty acids from storage areas within the fat cells to be used for
energy. This process is called lipolysis.
2. Sustains lipolysis by
"protecting" the chemical messenger, cAMP from breakdown. The secondary chemical messenger within the adipocyte that triggers
the release of fatty acids and their utilization for energy is called
cAMP, or cyclic AMP. ADIPO-X® v2.0 protects cAMP from breakdown
and keeps it alive longer within the cell, prolonging the fat loss process.
3. Prevents these fat loss hormones
from being broken down, allowing for continuous fat loss. ADIPO-X®
v2.0, like it's older brother, contains several ingredients that
prevent the breakdown of the fat-burning adrenal hormones by inhibiting
the enzymes COMT and MAO. This prolongs the life of epinephrine
and norepinephrine in the body, to prolong the fat burning process.
4. Inhibits alpha-receptor
activation. While targeting the Beta receptors of the fat
cell stimulated the release and burn of stored fat within the adipocyte,
stimulation of the alpha adrenergic receptors will shut down the process. ADIPO-X® v2.0 contains several ingredients included to prevent activation
of the alpha adrenergic receptors, to prevent the slow down of the fat
loss process.
5. Increases the thermogenic
uncoupling process. ADIPO-X® v2.0 supports thermogenesis, or the utilization of the fatty acids for energy,
once the stored fat released.
6. Blocks fat storage. The ingredients in ADIPO-X® v2.0 inhibit the synthesis from new fat by blocking the body's chemical
process for storing fat.
7. Ramps up metabolism by supporting
thyroid function. ADIPO-X® v2.0 supports the function of the thyroid, the body's metabolic regulation
center. By ensuring proper thyroid function, metabolism can be
enhanced, and ultimately fat loss is maximized.
SO WHAT'S NEW?
In addition to all that was great about
the original formula, ADIPO-X® v2.0 contains powerful new components that aid in process of maximizing fat
loss while improving performance, energy and focus.
Chocamine: a chemical derivative of chocolate, Chocamine contains specific key natural agents that mimic brain chemicals that govern appetite, alertness and mood. Chocamine is the reason why chocolate can produce euphoria, suppress appetite and have a stimulant-like effect.
Glucomannan (AmorphophallusKnojac): a soluble fiber derivative that helps with appetite control. Clinical studies show that Glucomannan can help curb appetite and contribute to fat loss. Glucomannan may also improve total cholesterol levels.
1,3-Dimethylamylamine: is a derivative of geranium oil which resembles the body's own chemical messenger epinephrine (adrenaline). Like adrenaline, 1,3-Dimethylamylamine is a powerful CNS stimulant increasing energy and clarity, especially valuable to athletes during calorie restriction or when a high level of focus is needed. Most importantly, it is also thought that 1,3-Dimethylamylamine works through a similar chemical pathway as ephedrine, causing a rise in cAMP, the chemical messenger that triggers fat release.
Yohimbine HCL: Yohimbine is an alpha receptor antagonist. As such, this potent herbal derivative helps with fat loss by helping to keep the lipolytic process rolling, ongoing 24/7. This is especially true in the body regions that are typically "problem areas" specific to gender. In women, these areas include the hips, thighs and butt, in med, it includes the midsection. Typically, fat cells in these gender-specific problem areas have a greater concentration of alpha receptors, compared to cells in other areas of the body. Yohimbine helps maximize fat loss especially in these areas.
This is especially true in the body
regions that are typically "problem areas" specific to gender. In women, these areas include the hips, thighs and butt, in med, it
includes the midsection. Typically, fat cells in these gender-specific problem areas have a greater
concentration of alpha receptors, compared to cells in other areas of
the body. Yohimbine helps maximize fat loss especially in these
areas. ADIPO-X® v2.0 contains the hydrochloride, standardized
version of Yohimbine, which ensures maximum potency with each and every
single dose.
Now available! Our limited edition "Competition Kit!"
Achieve that professional HARD, LEAN
and DRY "contest" condition! Each Competition kit contains a complete
30-Day "competition cycle":
● ADIPO-X® v2.0 - 4
week supply
● XTRACT - 72 hours
worth of the most potent high-definition diuretic available!
XTRACT is not simply some mild tealeaf and greens concoction that may or may
not work for you.
XTRACT is a whopping 1,700mg of
the most pure, most potent fluid-extracting agents available in nature. With more actives per dose, XTRACT will dry you out fast and
tight. But, to ensure the water stays where you need it and is
pulled only from where you don't (under the skin), XTRACT also
provides a full 1,000mg of balanced electrolytes.
XTRACT is the most-effective herbal
diuretic formula available. For high-definition fluid control,
there is no stronger product. Together with ADIPO-X®
v2.0, The Competition Kit will do more in 30-days to change the
look of your body than any other product you've ever used! We
guarantee it!
No matter what the occasion or event,
life is a competitive sport - play to win!
Use what the pro's use and show
up shredded! Get shrink-wrapped and skin-tight with ADIPO-X® Competition
Kit! No other formula is stronger for fat loss, appetite control
and high-power energy!

As a dietary supplement, start with a 1 capsule serving to evaluate tolerance and gradually increase to a full 2 capsule serving. Take one serving with 8 oz of water 30 to 60 minutes prior to breakfast on an empty stomach and an additional serving in the early afternoon on an empty stomach. Do not exceed 4 capsules in a 24 hour period. Do not take 6 hours prior to bed because ADIPO-X™ may interfere with sleep. Read entire label before using.
Store in a cool place. Protect from heat, light and moisture.
Contact us to add your own testimonial!
Akiba, T., K. Yaguchi, et al. (2004). "Inhibitory mechanism of caffeine on insulin-stimulated
glucose uptake in adipose cells." Biochem Pharmacol 68(10): 1929-37.
Banderet, L. E. and H. R. Lieberman (1989). "Treatment with tyrosine, a neurotransmitter
precursor, reduces environmental stress in humans." Brain Res Bull 22(4): 759-62.
Belza, A., E. Frandsen, et al. (2007). "Body fat loss achieved by stimulation of thermogenesis by a combination of bioactive food ingredients: a placebo-controlled,
double-blind 8-week intervention in obese subjects." Int J Obes (Lond) 31(1): 121-30.
Bhardwaj, R. K., H. Glaeser, et al. (2002). "Piperine, a major constituent of black
pepper, inhibits human P-glycoprotein and CYP3A4." J Pharmacol Exp Ther 302(2):
645-50.
Borea, P. A., K. Varani, et al. (1994). "Full and partial agonistic behaviour and
thermodynamic binding parameters of adenosine A1 receptor ligands." Eur J Pharmacol
267(1): 55-61.
Carlson, L. A., R. W. Butcher, et al. (1970). "Fat mobilizing lipolysis and levels
of cyclic AMP in human and dog adipose tissue." Acta Med Scand 187(6): 525-8.
Chanadiri, T., T. Sanikidze, et al. (2005). "[Effectiveness of green tea catechines
for the correction of the alimentary obesity in the experiment]." Georgian Med News(126):
61-3.
Chaudhry, A. and J. G. Granneman (1991). "Developmental changes in adenylyl cyclase
and GTP binding proteins in brown fat." Am J Physiol 261(2 Pt 2): R403-11.
Chaudhry, A. and J. G. Granneman (1997). "Effect of hypothyroidism on adenylyl cyclase
activity and subtype gene expression in brown adipose tissue." Am J Physiol 273(2
Pt 2): R762-7.
Chen, D., C. Y. Wang, et al. (2005). "Inhibition of human liver catechol-O-methyltransferase
by tea catechins and their metabolites: structure-activity relationship and molecular-modeling
studies." Biochem Pharmacol 69(10): 1523-31.
Choi, H. S. (2006). "Lipolytic effects of citrus peel oils and their components."
J Agric Food Chem 54(9): 3254-8.
Cui, J. and J. Himms-Hagen (1992). "Long-term decrease in body fat and in brown
adipose tissue in capsaicin-desensitized rats." Am J Physiol 262(4 Pt 2): R568-73.
Currie, P. J. and L. M. Wilson (1992). "Yohimbine attenuates clonidine-induced feeding
and macronutrient selection in genetically obese (ob/ob) mice." Pharmacol Biochem
Behav 43(4): 1039-46.
Diepvens, K., E. M. Kovacs, et al. (2005). "Effect of green tea on resting energy
expenditure and substrate oxidation during weight loss in overweight females." Br
J Nutr 94(6): 1026-34.
Diepvens, K., K. R. Westerterp, et al. (2007). "Obesity and thermogenesis related
to the consumption of caffeine, ephedrine, capsaicin, and green tea." Am J Physiol
Regul Integr Comp Physiol 292(1): R77-85.
Dolgacheva, L. P., B. B. Abzhalelov, et al. (2003). "Norepinephrine induces slow
calcium signalling in murine brown preadipocytes through the beta-adrenoceptor/cAMP/protein
kinase A pathway." Cell Signal 15(2): 209-16.
Dulloo, A. G., C. Duret, et al. (1999). "Efficacy of a green tea extract rich in
catechin polyphenols and caffeine in increasing 24-h energy expenditure and fat
oxidation in humans." Am J Clin Nutr 70(6): 1040-5.
Dulloo, A. G., J. Seydoux, et al. (2000). "Green tea and thermogenesis: interactions
between catechin-polyphenols, caffeine and sympathetic activity." Int J Obes Relat
Metab Disord 24(2): 252-8.
Galitzky, J., M. Lafontan, et al. (1993). "Role of vascular alpha-2 adrenoceptors
in regulating lipid mobilization from human adipose tissue." J Clin Invest 91(5):
1997-2003.
Galitzky, J., D. Riviere, et al. (1990). "Pharmacodynamic effects of chronic yohimbine
treatment in healthy volunteers." Eur J Clin Pharmacol 39(5): 447-51.
Galitzky, J., M. Taouis, et al. (1988). "Alpha 2-antagonist compounds and lipid
mobilization: evidence for a lipid mobilizing effect of oral yohimbine in healthy
male volunteers." Eur J Clin Invest 18(6): 587-94.
Gelenberg, A. J., C. J. Gibson, et al. (1982). "Neurotransmitter precursors for
the treatment of depression." Psychopharmacol Bull 18(1): 7-18.
Gomez-Ambrosi, J., G. Fruhbeck, et al. (2001). "Divergent effects of an alpha2-adrenergic
antagonist on lipolysis and thermogenesis: interactions with a beta3-adrenergic
agonist in rats." Int J Mol Med 8(1): 103-9.
Grunfeld, C. and J. K. Shigenaga (1984). "Nicotinamide and other inhibitors of ADP-ribosylation
block deoxyglucose uptake in cultured cells." Biochem Biophys Res Commun 123(2):
785-91.
Han, L. K., X. J. Gong, et al. (2005). "[Antiobesity actions of Zingiber officinale
Roscoe]." Yakugaku Zasshi 125(2): 213-7.
Harmer, C. J., S. F. McTavish, et al. (2001). "Tyrosine depletion attenuates dopamine
function in healthy volunteers." Psychopharmacology (Berl) 154(1): 105-11.
Hellstrom, L., S. Rossner, et al. (1997). "Lipolytic catecholamine resistance linked
to alpha 2-adrenoceptor sensitivity--a metabolic predictor of weight loss in obese
subjects." Int J Obes Relat Metab Disord 21(4): 314-20.
Ho, R. and Q. H. Shi (1982). "Forskolin as a novel lipolytic agent." Biochem Biophys
Res Commun 107(1): 157-64.
Ho, R. J. (1970). "Dependence of hormone-stimulated lipolysis on ATP and cyclic
AMP levels in fat cells." Horm Metab Res 2: Suppl 2:83-7.
Honnor, R. C., G. S. Dhillon, et al. (1985). "cAMP-dependent protein kinase and
lipolysis in rat adipocytes. II. Definition of steady-state relationship with lipolytic
and antilipolytic modulators." J Biol Chem 260(28): 15130-8.
Howald, H. and J. Decombaz (1983). "Nutrient intake and energy regulation in physical
exercise." Experientia Suppl 44: 77-88.
Imbeault, P., D. Prud'Homme, et al. (2000). "Adipose tissue metabolism in young
and middle-aged men after control for total body fatness." J Clin Endocrinol Metab
85(7): 2455-62.
Imbeault, P., A. Tremblay, et al. (2000). "beta-adrenoceptor-stimulated lipolysis
of subcutaneous abdominal adipocytes as a determinant of fat oxidation in obese
men." Eur J Clin Invest 30(4): 290-6.
Kawada, T., K. Hagihara, et al. (1986). "Effects of capsaicin on lipid metabolism
in rats fed a high fat diet." J Nutr 116(7): 1272-8.
Kawada, T., T. Watanabe, et al. (1986). "Capsaicin-induced beta-adrenergic action
on energy metabolism in rats: influence of capsaicin on oxygen consumption, the
respiratory quotient, and substrate utilization." Proc Soc Exp Biol Med 183(2):
250-6.
Kirchgessner, M., D. A. Roth-Maier, et al. (1995). "[B-vitamins (thiamine, vitamin
b6, pantothenic acid) in lean muscle tissue of growing cattle of the German Simmental
breed under different feeding intensities]." Z Lebensm Unters Forsch 201(1): 20-4.
Kobayashi, A., T. Osaka, et al. (1998). "Capsaicin activates heat loss and heat
production simultaneously and independently in rats." Am J Physiol 275(1 Pt 2):
R92-8.
Kucio, C., K. Jonderko, et al. (1991). "Does yohimbine act as a slimming drug?"
Isr J Med Sci 27(10): 550-6.
Lambert, J. D., J. Hong, et al. (2004). "Piperine enhances the bioavailability of
the tea polyphenol (-)-epigallocatechin-3-gallate in mice." J Nutr 134(8): 1948-52.
Le Corre, P., G. Dollo, et al. (1999). "Biopharmaceutics and metabolism of yohimbine
in humans." Eur J Pharm Sci 9(1): 79-84.
Lejeune, M. P., E. M. Kovacs, et al. (2003). "Effect of capsaicin on substrate oxidation
and weight maintenance after modest body-weight loss in human subjects." Br J Nutr
90(3): 651-59.
Lemonnier, D., P. de Gasquet, et al. (1974). "Effect of dietary vitamin B level
on fat storage, adipose tissue cellularity and energy expenditure in rats and mice
fed a high-fat diet." Nutr Metab 16(1): 15-29.
Lieberman, H. R., J. H. Georgelis, et al. (2005). "Tyrosine prevents effects of
hyperthermia on behavior and increases norepinephrine." Physiol Behav 84(1): 33-8.
Lin, Z., Y. Liao, et al. (2007). "Amides from Piper nigrum L. with dissimilar effects
on melanocyte proliferation in-vitro." J Pharm Pharmacol 59(4): 529-36.
Litosch, I., T. H. Hudson, et al. (1982). "Forskolin as an activator of cyclic AMP
accumulation and lipolysis in rat adipocytes." Mol Pharmacol 22(1): 109-15.
Lu, H., X. Meng, et al. (2003). "Enzymology of methylation of tea catechins and
inhibition of catechol-O-methyltransferase by (-)-epigallocatechin gallate." Drug
Metab Dispos 31(5): 572-9.
Malbon, C. C. and M. P. Graziano (1983). "Adenosine deaminase normalizes cyclic
AMP responses of hypothyroid rat fat cells to forskolin, but not beta-adrenergic
agonists." FEBS Lett 155(1): 35-8.
Masuda, Y., S. Haramizu, et al. (2003). "Upregulation of uncoupling proteins by
oral administration of capsiate, a nonpungent capsaicin analog." J Appl Physiol
95(6): 2408-15.
McNamara, F. N., A. Randall, et al. (2005). "Effects of piperine, the pungent component
of black pepper, at the human vanilloid receptor (TRPV1)." Br J Pharmacol 144(6):
781-90.
Melnyk, A. and J. Himms-Hagen (1995). "Resistance to aging-associated obesity in
capsaicin-desensitized rats one year after treatment." Obes Res 3(4): 337-44.
Mochizuki, M. and N. Hasegawa (2004). "Effects of green tea catechin-induced lipolysis
on cytosol glycerol content in differentiated 3T3-L1 cells." Phytother Res 18(11):
945-6.
Morimoto, C., Y. Satoh, et al. (2005). "Anti-obese action of raspberry ketone."
Life Sci 77(2): 194-204.
Muroyama, K., S. Murosaki, et al. (2003). "Effects of intake of a mixture of thiamin,
arginine, caffeine, and citric acid on adiposity in healthy subjects with high percent
body fat." Biosci Biotechnol Biochem 67(11): 2325-33.
Muroyama, K., S. Murosaki, et al. (2003). "Anti-obesity effects of a mixture of
thiamin, arginine, caffeine, and citric acid in non-insulin dependent diabetic KK
mice." J Nutr Sci Vitaminol (Tokyo) 49(1): 56-63.
Ohnuki, K., S. Haramizu, et al. (2001). "Administration of capsiate, a non-pungent
capsaicin analog, promotes energy metabolism and suppresses body fat accumulation
in mice." Biosci Biotechnol Biochem 65(12): 2735-40.
Ostman, J. (1964). "Effect Of Nicotinic Acid On The Fatty Acid Metabolism Of Adipose
Tissue In Alloxan Diabetic Rats." Metabolism 13: 675-80.
Ostman, J. (1965). "Inhibitory Effect Of Nicotinic Acid On Fat Mobilization In Alloxan-Diabetic
Rats. Ii. A Comparison Of The Effect Of Nicotinic Acid And Salicylate On The Fatty
Acid Metabolism And Glucose Uptake By Adipose Tissue In Vitro." Acta Med Scand 177:
623-9.
Papadelis, C., C. Kourtidou-Papadeli, et al. (2003). "Effects of mental workload
and caffeine on catecholamines and blood pressure compared to performance variations."
Brain Cogn 51(1): 143-54.
Rababah, T. M., N. S. Hettiarachchy, et al. (2004). "Total phenolics and antioxidant
activities of fenugreek, green tea, black tea, grape seed, ginger, rosemary, gotu
kola, and ginkgo extracts, vitamin E, and tert-butylhydroquinone." J Agric Food
Chem 52(16): 5183-6.
Razzoli, G. (1972). "[Effect of coffee on deposit lipids]." Minerva Med 63(61):
3361-2.
Roberts, S. A., J. M. Thorpe, et al. (2001). "Tyrosine requirement of healthy men
receiving a fixed phenylalanine intake determined by using indicator amino acid
oxidation." Am J Clin Nutr 73(2): 276-82.
Scarpace, P. J., L. A. Baresi, et al. (1987). "Modulation of receptors and adenylate
cyclase activity during sucrose feeding, food deprivation, and cold exposure." Am
J Physiol 253(6 Pt 1): E629-35.
Schimmel, R. J. (1980). "Interactions between catecholamines, methyl xanthines and
adenosine in regulation of cyclic AMP accumulation in hamster adipocytes." Biochim
Biophys Acta 629(1): 83-94.
Shixian, Q., B. VanCrey, et al. (2006). "Green tea extract thermogenesis-induced
weight loss by epigallocatechin gallate inhibition of catechol-O-methyltransferase."
J Med Food 9(4): 451-8.
Simon, E., M. T. Macarulla, et al. (2005). "Body fat-lowering effect of conjugated
linoleic acid is not due to increased lipolysis." J Physiol Biochem 61(2): 363-9.
Srinivasan, M. R. and M. N. Satyanarayana (1989). "Effect of capsaicin on skeletal
muscle lipoprotein lipase in rats fed high fat diet." Indian J Exp Biol 27(10):
910-2.
Szallasi, A. (2005). "Piperine: researchers discover new flavor in an ancient spice."
Trends Pharmacol Sci 26(9): 437-9.
Szilagyi, G., Z. Nagy, et al. (2005). "Effects of vinpocetine on the redistribution
of cerebral blood flow and glucose metabolism in chronic ischemic stroke patients:
a PET study." J Neurol Sci 229-230: 275-84.
Tam, S. W., M. Worcel, et al. (2001). "Yohimbine: a clinical review." Pharmacol
Ther 91(3): 215-43.
Tapsell, L. C., I. Hemphill, et al. (2006). "Health benefits of herbs and spices:
the past, the present, the future." Med J Aust 185(4 Suppl): S4-24.
Tornqvist, H., L. Krabisch, et al. (1972). "Rapid assay for hormone-sensitive lipase
activity of adipose tissue." J Lipid Res 13(3): 424-6.
Tsi, D., A. K. Nah, et al. (2003). "Clinical study on the combined effect of capsaicin,
green tea extract and essence of chicken on body fat content in human subjects."
J Nutr Sci Vitaminol (Tokyo) 49(6): 437-41.
Verma, S. K. and A. Bordia (2001). "Ginger, fat and fibrinolysis." Indian J Med
Sci 55(2): 83-6.
Walldius, G. and G. Wahlberg (1985). "Effects of nicotinic acid and its derivatives
on lipid metabolism and other metabolic factors related to atherosclerosis." Adv
Exp Med Biol 183: 281-93.
Westerterp-Plantenga, M., K. Diepvens, et al. (2006). "Metabolic effects of spices,
teas, and caffeine." Physiol Behav 89(1): 85-91.
Wolfram, S., Y. Wang, et al. (2006). "Anti-obesity effects of green tea: from bedside
to bench." Mol Nutr Food Res 50(2): 176-87.
Wu, A. H., C. C. Tseng, et al. (2003). "Tea intake, COMT genotype, and breast cancer
in Asian-American women." Cancer Res 63(21): 7526-9.
Yoshida, T., K. Yoshioka, et al. (1988). "Effects of capsaicin and isothiocyanate
on thermogenesis of interscapular brown adipose tissue in rats." J Nutr Sci Vitaminol
(Tokyo) 34(6): 587-94.
Zhang, L. L., D. Yan Liu, et al. (2007). "Activation of transient receptor potential
vanilloid type-1 channel prevents adipogenesis and obesity." Circ Res 100(7): 1063-70.