Muscle Building Stack

5/5

Only $209.95!

20-E + EP-11

• Build muscle
• Boost strength
• Create new muscle fibres
• Increase muscle fullness
• Better pumps
• Increase vascularity
• Increase performance
• Break plateaus

96 in stock

$129.95

44 in stock

$109.95

44 in stock

Category

Description

20-E | EDIBLE OIL
MUSCLE BUILDING

“Get the Popeye effect!”

20-E is formulated with 20-hydroxyecdysone, a muscle building plant compound found in spinach and quinoa. 20-E is best used for maximising strength. APO Compounds has infused 20-hydroxyecdysone in a patented delivery system for enhanced bioavailability. 20-E assists with:

• Build muscle rapidly
• Boost strength dramatically
• Create new muscle fibres
• Increase muscle fullness
• Better pumps
• Increase vascularity
• Increase performance
• Break plateaus
• Reduce recovery time
• Burn fat
• Reduce estrogen
• Reduce water retention
• Support tendons and ligaments

Natural, safe, effective
• Safe for women
• Exists in nature
• Derived from plants
• No masculinising side-effects
• No liver toxicity
• No PCT needed

★★★★★ STRENGTH
★★★☆☆ SIZE
★★☆☆☆ FAT-LOSS
★★☆☆☆ BODY RECOMP

Daily Dose Equivalence
1.2KG OF BABY SPINACH

 


 

The Key Ingredients of 20-E

  • Cyanotis Arachnoides Extract (Standardised 98% 20-Hydroxyecdysone)
  • Liquid Formula 11615™ (445, 433, 1521)

 


 

EP-11 | EDIBLE OIL
MUSCLE BUILDING 

EP-11 is formulated with l-epicatechin, a plant muscle building compound found in green tea and cocoa beans. EP-11 is best used for maximising size. APO Compounds has infused l-epicatechin in a patented delivery system for enhanced bioavailability. EP-11 assists with:

• Build muscle rapidly
• Boost strength dramatically
• Grow existing muscle fibres
• Increase muscle fullness
• Better pumps
• Increase performance
• Break plateaus
• Reduce recovery time

Natural, safe, effective
• Safe for women
• Exists in nature
• Derived from plants
• No masculinising side-effects
• No liver toxicity
• No PCT needed

★★★★☆ STRENGTH
★★★★★ SIZE
☆☆☆☆☆ FAT-LOSS
★★☆☆☆ BODY RECOMP

Daily Dose Equivalence
38 CUPS OF GREEN TEA

 


 

The Key Ingredients of EP-11

  • Theobroma Cocoa Bean Extract (Standardised 98% l-Epicatechin)
  • Liquid Formula 11615™ (445, 433, 1521)

Directions

20-E Directions For Use:
Take 2.3mL twice daily mixed in water, milk, or juice by stirring vigorously, shaking, or blending. The food must be consumed with an appropriate fluid intake of one cup. If used during exercise, the food should be consumed in accordance with directions to avoid the possibility of gastro-intestinal upset.

This food is not a soul source of nutrition and should be consumed in conjunction with a healthy diet and regular exercise. This product is a high fat food and should be used for special fat loading strategies.

KEEP OUT OF REACH OF CHILDREN. Not suitable for children under the age of 18 years. Do not use if you are pregnant or breastfeeding. If you are taking medications seek medical advice before consuming this product.

This product does not claim to the prevention, diagnosis, cure, or alleviation of a disease, disorder or condition, or represented in any way to be for therapeutic use or is likely to be taken to be for therapeutic use; whether because of the way in which the food is presented or for any other reason.

 


 

EP-11 Directions For Use: Take 2.3mL twice daily mixed in water, milk, or juice by stirring vigorously, shaking, or blending. The food must be consumed with an appropriate fluid intake of one cup. If used during exercise, the food should be consumed in accordance with directions to avoid the possibility of gastro-intestinal upset.

This food is not a soul source of nutrition and should be consumed in conjunction with a healthy diet and regular exercise. This product is a high fat food and should be used for special fat loading strategies.

KEEP OUT OF REACH OF CHILDREN. Not suitable for children under the age of 18 years. Do not use if you are pregnant or breastfeeding. If you are taking medications seek medical advice before consuming this product.

This product does not claim to the prevention, diagnosis, cure, or alleviation of a disease, disorder or condition, or represented in any way to be for therapeutic use or is likely to be taken to be for therapeutic use; whether because of the way in which the food is presented or for any other reason.

Nutritional

20-E | MSMB

 

EP-11 | MSMB

Accreditation

Complimentary Medical Association Approved Supplier for 2019

Silver Member of the International Alliance of Holistic Therapists for 2019

 

20-E | MSMB

  1. Hirunsai, M., Yimlamai, T. & Suksamrarn, A. 2016. Effect of 20-Hydroxyecdysone on Proteolytic Regulation in Skeletal Muscle Atrophy. International Journal of Experimental and Clinical Pathophysiology and Drug Research, 30(6), pp. 869-877. DOI: 10.21873/invivo.11007
  2. Sheu, S. Y., Ho, S. R., Sun, J. S., Chen, C. Y. & Ke, C. J. 2015. Arthropod steroid hormone (20-Hydroxyecdysone) suppresses IL-1β- induced catabolic gene expression in cartilage. BMC Complementary and Alternative Medicine, 15(1). DOI: 10.1186/s12906-015-0520-z
  3. Parr, M. K., Botre, F., Nab, A., Henjevoss, J., Diel, P. & Wolber, G. 2015. Ecdysteroids: A novel class of anabolic agents? Biology Of Sport, 32(2), pp. 169-173. DOI: 10.5604/20831862.1144420
  4. Gorelick-Feldman, J., MacLean, D., Ilic, N., Poulev, A., Lila, M. A., Cheng, D., & Raskin, I. 2008. Phytoecdysteroids increase protein synthesis in skeletal muscle cells. Journal Of Agriculture And Food Chemistry, 56(10), pp. 3532-3537. DOI: 10.1021/jf073059z
  5. Gorelick-Feldman, J., Cohick, W., & Raskin, I. 2010. Ecdysteroids elicit a rapid Ca 2+ flux leading to Akt activation and increased protein synthesis in skeletal muscle cells. Steroids, 75(10), pp. 632-637. DOI: 10.1016/j.steroids.2010.03.008
  6. Syrov, V. N. & Kurmukov, A. G. 1976. Anabolic activity of phytoecdysone-ecdysterone isolated from Rhaponticum carthamoides (Willd.) Iljin. Farmakol Toksikol, 39(6), pp. 690-603. PMID 1030669
  7. Parr, M. 2016. Ecdysteroids As Non-Conventional Anabolic Agents: Pharmacodynamics, Pharmacokinetics, And Detection OfEcdysterone. World Anti-Doping Agency. Freie Universität Berlin, Germany. Online Publication
  8. Tiidus, P. M., Lowe, D. A. & Brown, M. 2013. Estrogen replacement and skeletal muscle: mechanisms and population health. Journal of Applied Physiology, 115(5), pp. 569. DOI: 10.1152/japplphysiol.00629.2013
  9. Velders, M., Schleipen, B., Fritzemeier, K. H., Zierau, O. & Diel, P. 2012. Selective estrogen receptor-β activation stimulates skeletal muscle growth and regeneration. The FASEB Journal, 26(5), pp. 1909-1920. DOI: 10.1096/fj.11-194779
  10. Weihua, Z., Saji, S., Mäkinen, S., Cheng, G., Jensen, E. V., Warner, M. & Gustafsson, J. A. 2000. Estrogen receptor (ER) beta, a modulator of ERalpha in the uterus. Proceedings of the National Academy of Sciences of the United States of America, 97(11), pp. 5936-5941. DOI: 10.1073/pnas.97.11.5936

 

EP-11 | MSMB

  1. McDonald, C., Henricson, E., Oskarsson, B., Aguilar, C., Nicorici, A., Joyce, N., Reddy, D., Wagner, A., deBie, E., Goude, E., Abresch, R., Villareal, F., Perkins, G., Hathout, Y., Dugar, S. & Schreiner, G. 2015. Epicatechin enhances mitochondrial biogenesis, increases dystrophin and utrophin, increases follistatin while decreasing myostatin, and improves skeletal muscle exercise response in adults with Becker muscular dystrophy (BMD). Neuromuscular Disorders. DOI: 10.1016/j.nmd.2015.06.456
  2. Gutierrez-Salmeana, G., Ciaraldi, T. P., Nogueira, L., Barboza, J., Taub, P. R., Hogan, M. C., Henry, R. R., Meaney, E., Villarreal, F., Ceballos, G. & Ramirez-Sancheza, I. 2014. Effects of (−)-epicatechin on molecular modulators of skeletal muscle growth and differentiation. The Journal of Nutritional Biochemistry, 25(1), pp. 91-94. DOI: 10.1016/j.jnutbio.2013.09.007
  3. Li, P., Liu, A., Xiong, W., Lin, H., Xiao, W., Huang, J., Zhang, S. & Liu, Z. 2019. Catechins enhance skeletal muscle performance. Critical Reviews in Food Science and Nutrition. DOI: 10.1080/10408398.2018.1549534
  4. Jäger, A. K. & Saaby, L. 2011. Flavonoids and the CNS. Molecules, 2011(16), pp. 1471-1485. DOI: 10.3390/molecules16021471

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