How Shredded3 Works, Breaking Down The Science.

<img src="Shredded3.jpg" alt="Alchemy Labs Shredding Stack">


Shredded3 is one of our top selling hormones, designed for weightlifters and bodybuilders who are looking to destroy build lean muscle and rip off unwanted body fat.*

When it comes to Andro based pro-hormones, one big factor comes into play.. Absorption. Did you know that most Andro's never make it pass the first pass of the liver, and you never actually get the full dose you need. We have helped solved this issue with out Rocket Delivery system to bypass stomach acids and allow for maximum absorption, which combats the common absorption issues with Andro-based pro hormones.*

What's this mean for you? This means that you are able to take in the full dosage of our pro-hormones and whenever you experience Shredded3 for the first time, you will immediately notice increased "Alpha Male" feeling.  Many users note that they notice significant gains in strength, muscle size, and reduction in body fat while running Shredded3.*

Let's jump into the ingredients of SHREDDED3 and figure out what makes it work so well. 

<img src="Review.jpg" alt="Alchemy Labs Shredded3 review">

Epi-Androsterone: 5a-Androstan-3b-ol-17-one

To start: Epi-Andro is highly anabolic, which makes it a great choice for bulking or cutting cycles. However, Epi-Andro tends to be used more for those trying to develop a leaner, more muscular physique. Generally speaking, users note that that notice differences in their physique within the first couple weeks of taking it, and report muscle density, strength, and loss is body fat.

How Does Epi-Androsterone Work?

To really get the max out of any cycle you are going to run with Epi-Androsterone or (EpiAndro) you may want to know how it is believed to work inside the body.

First thing to know Epi-Andro is a derivative of Dehydroepiandrosterone (DHEA).  When you absorbed it into the body, it then converts into Dihydrotestosterone (DHT) which is the primary Androgen in men.

DHT is most popular for its abilities to increase strength, reduce water retention, drop body fat and build dense muscle mass. DHT also can help reduce estrogen conversion in the body, which leads helping promote dry, hard muscles and aid in the loss of body fat.

Since Epi-Andro is converting into DHT inside the body, users often report that they find it working almost immediately. Generally reports from users come in from the first week stating they have noticeable increases in libido, strength, muscle hardness, and have a more shredded look.

The second great part of this compound is its ability to bind to SHBG or Sex Hormone-Binding Globulins. Which allows your body to unlock a higher ration of free testosterone. Obviously we all know that testosterone is the king of hormones inside our bodies for building muscle and greater strength! 

DHEA: Dehydroepiandrosterone

So DHEA or Dehydroepiandrosterone may be one of the most underrated ingredients for packing on muscle, and fat loss.

DHEA is produced in the adrenal glands and is the most abundant hormone in the body, because it gets converted into around 20 different hormones. 

Unfortunately, after the age of 25 DHEA levels seem to start declining as well as muscle mass and strength. Studies have show that DHEA has been a beneficial effect for enhancing the increases in muscle mass and strength when coupled with heavy resistance training (1).

For men, one of the biggest benefits from DHEA is, elevated testosterone levels. Several studies now days, have shown that DHEA can increase testosterone levels in older man, which can lead to greater muscle growth, sex drive and strength. Which if you a guy over 25 reading this, it's a must have!

Newer studies are coming out showing that DHEA may be able to increase Insulin Like Growth Factor-1 (IGF-1).

Does DHEA Work For Fat Loss?

Recent research in animials and humans have found that DHEA may help reduce body fat. The studies show that DHEA helps men lose body fat by engaging the receptor known as peroxisome proliferator-activator receptor alpha. Activating PPAR and genes that decrease fat storage's inside the human body. 

The second way DHEA is believed to reduce body fat is by increasing insulin sensitivity. This study shows that when taking DHEA everyday for six months, users noticed reductions in body fat ad lower insulin level... Meaning that their bodies are able to partition glucose better and drive it into the muscle cells. (2)

DIM: Diindolymethane

Dinndolymethane or otherwise known as DIM, is a powerfl nutrient found in broccoli, and cauliflower. DIM has direct effects on the hormonal balance and can reduce the negative effects from excess estrogen in the body. There is a full list of benefits from DIM like: Weight loss, preventing negative side effects from testosterone supplementation, helping hormonal acne, etc. 

DIM works by blocking the enzyme that converts testosterone into estrogen. Secondly, it converts bad estrogen into good estrogen metabolites inside the body. 

If you are familiar with estrogen, you know that it is a female hormone that increases as we age, and is responsible for making us hold onto more body fat, water weight, and reduces our energy levels. 

Will DIM Help Reduce Estrogen and Boost Testosterone?

Here's the deal, everyone has testosterone and if you are reading this. You know that testosterone is obviously king for muscle mass and strength. Now, as testosterone decreases with stress or age and your body will produce more aromatase, which convert a portion of testosterone into estrogen (3). Now DIM, inhibits aromatase inside the body. This allows more testosterone to be free inside your system. Meaning more strength, more muscle, and greater fat loss.*


 Why You Should Take SHREDDED3 For Your Next Cycle:

If you are someone who is tired of staying at the same weights in the gym, or tired of looking in the mirror to see the same thing everyday.. Then SHREDDED3 is for you.

Click Here to learn more about it, and how it can help you reach your physique goals. 






(1)  2006 Nov;291(5):E1003-8. Epub 2006 Jun 20. 

(2) JAMA. 2004;292(18):2243-2248. doi:10.1001/jama.292.18.2243

(3)  2006 Feb;98(2-3):133-8. Epub 2005 Dec 28.