S-4 50mg *
MK-677 25mg *
GW-501516 20mg *
Trestolone 25mg *
Combined with a Liver support as well as anti-estrogen compound!!
What is Dimethandrostenol?
Dimethandrostenol (2,17α-dimethyl-17β-hydroxy-5α-androst-2-ene) was brought to the market by Iron Legion Supplements in 2013 in their product Mithras. Dimethandrostenol is part of the 2-methyl group which includes some of the most popular prohormones ever including Superdrol, Pheraplex, Methylstenbolone, and Methyl-1-Testosterone aka M1T. All of these compounds have been considered to be the cream of the crop when it comes to bulking prohormones. In regards to its structure, it is considered to be a cross between Superdrol and Pheraplex.
What is Trestolone?
Trestolone, also known as MENT, is one of the more potent steroids/hormones created to date. It is a 19Nor hormone, which makes it a derivative of nandrolone (which is the base steroid in Deca). On paper, trestolone is WAY stronger than testosterone. Its androgenic/estrogenic character will be similar to those of Tren and Deca, but it’s muscle building hypertrophic ability should be higher than both of the above mentioned compounds.
Stacked deal of medfit rx SARMS and Pro-Hormones! Only the best legal sarms and pro hormones!
The Key Benefits of S4 (Andarine)
S-4 is by far the most versatile SARM ever created. Not only is it the first SARM approved for a stage 2 research study, but it has also become the most analyzed and investigated SARM so far. After the discovery of its anabolic potential, the primary purpose of S-4 aimed to develop an alternative treatment to age-related muscle wasting, osteoporosis, and similar symptoms of hypogonadism, or end-stage renal disease.
Aside from preserving lean body mass, S4 can also help improve it.
From a stage 1 study, S-4 has provided evidence of a 3.3 lbs increase in less than 90 days with no increases exercise or change in daily diet. An unintended side effect (or benefit if you will) is the decrease in body fat [Chen et al., 2005; Gao et al., 2005; Kearbey et al., 2007]. Decreases in body fat are dependent on the person’s genetics, but it will definitely have strong effects on the body’s ability to oxidize fatty tissue. S-4 was found to not only have a great affinity (potency in binding to androgen receptors), while also presenting greater anabolic effects than some traditional steroids [Kearbey et al., 2007].
Aside from its muscle building advantages, S4 won’t cause liver damage, can prevent gynecomastia (enlarged breasts in men) and can help boost your overall health.
Here are some of the other benefits of Andarine that are worth noting:
- Very minimal growth on secondary sexual organs such as the prostate.
- The LDL/ HDL ratio is not affected which makes it a low cardiovascular risk.
- 0% chance of aromatization, male breast lactation, or rise in any other female characteristic during the post cycle recovery. [Kearbey et al., 2007]
- Testosterone is not diminished in any capacity during the post cycle recovery.
- Very exclusive in tissue selection and growth which means it will not cause heart enlargement or damage to neighboring organs.
- SARMs do NOT require the utilization or devouring of liver enzymes to activate their anabolic effects. This eliminates any risk of hepatotoxicity or hepatitis.
- Although SARMs such as S-4 are not as powerful as comparable steroids such as Winstrol, they do not require the extensive post cycle therapy and can be cycled back to back throughout the year. Over the course of a year, obtaining the same results is very possible.
- SARMs is very female friendly and does not cause excessive masculine features such enlarged sexual characteristics.
- S-4 has overall presented larger increases in muscle mass than DHT
What is Ibutamoren
Ibutamoren is frequently discussed on online forums for its muscle-building properties. It is available over the counter and used by those wishing to increase their growth hormone levels.
However, clinical studies of this compound are relatively few. In the text below, we will highlight what is known about ibutamoren so far.
Ibutamoren increases growth hormone levels by mimicking the action of the hormone ghrelin and binding to one of the ghrelin receptors (GHSR) in the brain. Activated GHSR stimulates growth hormone release from the brain.
GHSR is found in brain regions that control appetite, pleasure, mood, biological rhythms, memory, and cognition [R]. Therefore, we can expect that ibutamoren may also affect these functions. However, so far, clinical studies describe only the effects ibutamoren has on appetite – and as expected, like ghrelin, ibutamoren increases it.
A great thing about ibutamoren is that it increases growth hormone levels with little or no increase in other hormones, such as cortisol [R, R]. Cortisol suppresses the immune system, reduces wound healing, and impairs learning and memory, and it’s usually not good to have this hormone elevated.
What Is Cardarine?
GW501516 is a chemical that was recently developed by GlaxoSmithKline for its potential benefits on the heart, blood vessels, and diabetes. However, studies were halted in Phase II on animals because it caused cancers [R].
One could argue that cancer risks have not been proven in humans. But the main reason is precisely that it was not shown to be safe even in animals, and because substances usually have to be given over a longer period of time to demonstrate cancerous effects.
But how did scientists discover Cardarine (less elegantly known as GW501516) in the first place?
It’s no secret that our modern inactive lifestyle too often causes many metabolic problems, such as diabetes, inflammation, and heart disease. In the search for substances that could somehow speed up fat burning and increase physical endurance, scientists turned to the PPAR delta pathway.
Activation of PPAR delta can increase energy, fat burning, muscle building, endurance, and blood lipids. Cardarine binds to and activates the peroxisome proliferator activator receptor delta (PPAR delta). A lot of PPAR delta is in the muscles, and it activates many genes important for energy use (R).
Activating PPAR delta could play a role in building muscles, improving heart health, boosting metabolism, and reducing inflammation. Targeting this pathway with Cardarine seems promising. But researchers refer to GW501516 as a failed “exercise mimetic”, because of its unfortunate cancer-promoting side effects [R+].
Note: By writing this post, we are not recommending this drug. Some of our readers who were already taking the drug requested that we commission a post on it, and we are simply providing information that is available in the scientific literature. Please discuss your medications with your doctor.