Benefits:

  • Supports Increases in Lean Mass*
  • Helps Increase Muscle Hardness*
  • Supports Increased Strength*
  • Zero Conversion to Estrogen*
  • Helps Improve Muscle Definition*
  • Helps Increase Muscle Pumps*
  • Supports Fat Loss*
  • Supports Increased Protein Synthesis*

What's in it?:

1-Androsterone: This ingredient is a DHEA derivative that goes through a double conversion process to become 1-AD, also known as 1-testosterone, a compound that is 7 times more anabolic than testosterone. There is no conversion to estrogen with this compound so water retention is a non-factor. Additionally, as the muscle increases are dry in nature, gains are fairly easy to sustain during and after post cycle therapy.

Bergamottin: This is a substance naturally found in grapefruit and is a natural inhibitor of an enzyme found in the liver and intestines called CYP3A4. This enzyme plays a role in removing 1-Androsterone from your body and breaks it down very fast causing much of the compound to just pass through your system. With Bergamottin inhibiting this process, the compounds break down is significantly reduced allowing for more of it to be absorbed into the bloodstream.

Cyclosome Delivery Technology: Researchers at Hi-Tech recently developed a proprietary process called Cyclosome™ Technology. This one-of-a-kind technology brought to you by the leaders in Prohormones involves the entrapment of hydrophobic prohormones and other Testosterone boosting compounds in the form of water-soluble Prohormone–cyclodextrin (CD) complex in liposomes has been investigated as a new strategy to combine the relative advantages of CDs and liposomes into one system, namely Prohormone-in-CD-in-liposome systems called Cyclosome's™. You can think of all this in terms of a ‘Trojan Horse,’ passing through the liver unharmed and intact. As opposed to being destroyed in the liver like all other hormonal products on the market, past and present. This new Cyclosome™ technology allows the ‘Trojan Horse’ to deliver prohormones and testosterone boosters to the systemic circulation by the intestinal lymphatic route, circumventing first-pass inactivation in the liver for the very first time

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