SARM'S

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Selective Androgen Receptor Modulator

Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs but be much more selective in their action, allowing them to be used for more uses than the relatively limited legitimate uses of anabolic steroids. Wikipedia

Synonyms: Partial androgens Use: Hypogonadism, Osteopenia, Osteoporosis, Sarcopenia, Cachexia Biological target: Androgen receptor


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Ostarine MK-2866

Descriptions and Benefits

MK-2866, also known as Ostarine or Enobosarm, is one of the best-studied SARMs. It is a non-steroidal selective androgen receptor modifier that strengthens muscle, bone, and tendons. It does not have the negative side effects associated with testosterone such as raising liver, kidney, and prostate enzymes. Elderly men and women who took modest doses of Ostarine for 12 weeks grew 3 pounds of muscle and lost a pound of fat, with no changes to diet or exercise.

Concentration

25mg/ml.

Half Life

24 hours.


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RAD-140 (TESTOLONE)

Description and Benefit

RAD-140, also known as Testolone, is a SARM, a selective androgen receptor modulator. There is little danger of nonskeletal muscle tissues experiencing androgen activity. In fact, RAD-140 has the highest ratio of anabolic to androgenic activity of any SARM discovered, 90:1.

Testosterone has an anabolic to androgenic ratio of 100:100. This means that Testolone is almost as anabolic as testosterone while being only 1/100th as androgenic. This is a positive as most of the negative side effects of testosterone, including effects on liver, kidney and prostate, come from its androgenic effects.

Concentration

15mg/ml.

Half Life

16 hours.


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MK-677 (NUTROBAL)

Descriptions and Benefits

MK-677, also known as Ibutamoren or Nutrobal, is commonly referred to as a SARM, a selective androgen receptor modulator, but it is actually a Human Growth Hormone secretagogue, meaning that it stimulates the pitutary gland to secrete HGH.

MK-677 has been shown to increase fat-free mass; enhance sleep quality; improve healing of muscle, bone and ligaments; lower LDL cholesterol; improve hair and skin appearance; and improve overall sense of well-being.

MK-677 does not cause pituitary sensitization, nor does it suppress the body’s production of Growth Hormone.

Because Ibutamoren doesn’t stimulate testosterone, there are no chances of aromatization, or danger to liver, kidney, or prostate.

Concentration MORE INFO.

25mg/ml.

Half Life

24 hours.



GW-501516 (CARDARINE)

Descriptions and Benefits

GW-501516, also known as Cardarine, is a PPAR agonist that has been shown to have positive effects on muscle building, endurance, increased HDL (good) and decreased LDL (bad) cholesterol, and body recomposition.  Cardarine currently has no human studies, but rodent studies have been very encouraging.

When combined with exercise, GW-501516 combined with four weeks of running increased running time by 68%; running distance by 70%; and doubled overall muscular endurance. Along with exercise GW-501516 increased mitochondrial growth by 50%. Additionally, GW-501516 on its own has been found to activate many of the genes that activate when an organism goes for a run or exercises.

Cardarine is not hormonal so it is not suppressive of endogenous testosterone.

Concentration

10mg/ml.

Half Life

20 – 24 hours.

Dosage

10 – 20mg in an 8-week cycle. MORE INFO.



LGD-4033 (LIGANDROL)

Descriptions and Benefits

LGD-4033, also known Ligandrol, is a SARM that has been shown to have positive effects on muscle building, body recomposition, sex drive, and bone density. Already in human trials, Ligandrol has been shown to be highly selective for muscle and bone cells, largely ignoring prostate or sebaceous cells. This makes the side effects for LGD-4033 minimal.

Florida Gators quarterback Will Grier allegedly used Ligandrol to add 43 pounds of muscle in one year.

Concentration

10mg/ml.

Half Life

24 – 36 hours.


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SR9009 (STENABOLIC)

Descriptions and Benefits

SR9009, also known as Stenabolic, is a SARM that was developed at the Scripps Research Institute. It is a PPAR alpha modifier very similar GW­-501516. It binds to the Rev-erbα protein, which influences lipid and glucose metabolism in the liver and the creation of fat-storing cells.

Stenabolic has been found to increase mitochondria, the powerhouses of your cells. Once mice were given Stenabolic, they were able to run for 50% longer than non-treated mice. It has also been found to aid weight loss.

Concentration

20mg/ml.

Half Life

2.5 hours


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S4 (ANDARINE)

Benefits and Description

S4, also known as Andarine, Andarin, S-40503, or GTx-007, is a SARM that selectively binds to androgen receptors in skeletal muscle tissue. There is little danger of nonskeletal muscle tissues experiencing androgen activity.  Additionally, research has shown it does not cause aromatization (conversion of testosterone into estrogen), liver strain, or severe HPTA (hypothalamic pituitary testicular axis) suppression. Aside from building lean body mass, andarine is also used for benign prostatic hypertrophy, muscle wasting, and osteoporosis.

Concentration

50mg/ml.

Half Life

4 – 6 hours.


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YK-11

Descriptions and Benefits

YK-11 although lumped into the SARM category is actually a myostatin inhibitor. Myostatin inhibits muscle growth. By inhibiting the inhibitor, YK-11 promotes rapid muscle growth. YK-11 has been shown to be more anabolic than dihydrotestosterone (DHT).

Although just discovered in 2011, YK-11 is quickly developing a reputation as the most powerful SARM.

Concentration

10mg/ml.

Half Life

6 – 10 hours.


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*These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease. THE CONTENT ON THIS PAGE IS FOR INFORMATIONAL PURPOSES ONLY.

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