S4 (Andarine) or Acetamidoxolutamide
Profile, Usages and all the info you need to know
Originally written and Posted at sarmstore
POSTED ON SEPTEMBER 9, 2015 BY The ADMIN of the site
Thank you SS Admin for this great write up!

S4 (Andarine) or Acetamidoxolutamide
, is a SARM (Selective Androgen Receptor Modulator). S4 is said to be the most potent SARM which helps sustain lean muscle mass while stimulating fat elimination at the same time. Today, we’ll take a closer look on everything there is to know about S4.
What is S4?

To start, let’s describe what a SARM does. There are three type of chemicals that act on the androgen receptor (AR). One is the an AR antagonist, which is a chemical that binds to the receptor to prevent it from activating. The second is an AR agonist, which binds to the receptor and detaches, then binds again, over and over. An example of an AR agonist is testosterone, each time the AR is bonded with testosterone, a signal is sent out to activate a particular set of genes. The more testosterone that is in the system, the more AR binding will occur. The third is an AR modulator, or basically a molecule that attaches to an AR and changes its structure to react however it wants.
How S4 Works

A SARM such as S-4 is a good example. S-4 attaches to the AR and sticks to it; each time the AR interacts with testosterone, S-4 forces it to produce genes that exclusively benefit muscle and bone growth. In other words, S4 is a form of SARM that attaches to the androgen receptor (AR) the same with regular androgens, the only variation is that S4 generates selective anabolic activity.
S4 Chemical Composition
As said earlier, SARMS function by tying to the AR resulting to anabolic activity. Due to this fastening and stimulation, more protein is produced which allows muscle building. S4 can trigger muscle development in the same way as steroids, but minus the same unwanted side effects, the latter has on the prostate and other sexual organs.
S4 is a SARM with utmost androgenic effects as it around 33% of the strength of testosterone when attaching to AR. S-4 also increases the amount of muscle mass produced by desensitizing the AR to the individual’s natural testosterone to influence a stronger effect.
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, it has 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.
History and Development of S4

The idea for S-4 didn’t start out as many believe. It wasn’t an attempt to create a safer version of steroids orany of that nonsense people use to sell anabolics. S-4 started out as a new development for male contraceptives and showed some promising effects. There had been decreases in spermatogenesis and an increase in male libido. So for those of you who have had trouble getting your wife pregnant while on sarms…you’re welcome.
It wasn’t until researchers discovered how this first generation SARM affected castrated lab mice by not only increasing the production of muscle mass and calcium for bone density, but was also completely selective in its tissue growth. As studies continued, many of these research trials resulted in astonishing outcomes creating a benchmark for even more research.
One study in particular compared S-4 to DHT (a common anabolic steroid); the results have shown that S-4 exceeded DHT in producing lean muscle mass over the course of 120 days with only 3mg per day. S-4 has also shown no side effects on prostate growth, testosterone shut down, or any negative side effects caused by traditional anabolic steroids [Kearbey et al., 2007]. Another study identified that S-4 is completely absorbed even at very low doses. The half-life for S-4 is between 2.6 to 5.3 hours. Most people have opted to split their 50mg to 75mg doses into 3 separate doses, one with every meal. This has become somewhat of a dogma but there are now studies proving that it is any more effective than one solid dose once a day [Chen et al., 2005a; Gao et al., 2004; Gao et al., 2005; Kearbey et al., 2007; Kearbey et al., 2004].
Once more, an early study done on S-4 provided proof of full muscle regeneration in volunteers with with degenerative disorders without the use of exercise and the minimum dosage of 3mg/kg/day. Changes can be seen anywhere from 1-2 weeks. This was the very first study classified S-4 as CLINICALLY SIGNIFICANT by improving skeletal muscle strength, lean body mass, and a reduction in body fat [Chen et al., 2005; Gao et al., 2005; Kearbey et al., 2007]. Unfortunately, there are always some side effects that arise when using Because S-4 is a ligand by definition, the side effects will never be permanent even at supraphysiological dosages and can be easily avoided through proper dosing.
How Andarine is used will depend on the kind of results you want. Here are the general guidelines…Right Dosing

  • S-4 should be taken at 50mg-75mg, 5 days out of the week, for 12-16 weeks. As mentioned before, S-4 does not need to be taken on 3 separate occasions throughout the day; but for individuals that prefer this method, a 25mg dose (roughly half a milliliter) is recommended once with each of your three main meals.
  • Once again, as mentioned above, S-4 does have point of diminishing returns. This means usage of S-4 passed 75mg or usage of S-4 for more than 16 weeks will not result in any added muscle mass. There will not be an increase in side effects either, but you will be running the risk of AR desensitization and inevitably wasting your product.
  • Dosing with S-4 for less than 6-8 weeks is not recommended and will not allow the researcher to witness the full benefits of the product.

Recommended dose for cutting is 50 mg for 6-8 weeks. You should use it every day then take 2 days off for the duration. Taking S4 daily for the length of the cycle can lead to changes in eyesight.Uses of Andarine

For Cutting (best use of S4)Andarine’s properties are very alike with steroids Anavar and Winstrol, the only difference is that S4 can better provide lean muscle gains. In fact, there have been many cases of bodybuilders gaining up to 3 pounds of lean muscle while on a caloric deficit! S4 displays the same binding resemblance to AR, hence presenting similar fat burning effects. S4 can also minimize LPL (lipoprotein lipase) – an enzyme that causes lipid accumulation and plays a role in storing adipose tissue (excess body fat). The AR oxidizes this adipose tissue and uses it as its preferred energy source, allowing the body to decrease excess fat at an amazing rate.It also improves vascularity for that “aesthetic” chiseled look with minimal to no water retention. Unlike steroids, it won’t affect your joints but reinforce muscle mass and power instead. You can also say goodbye to painful pumps.Recommended Dosage: 50 mg for 6-8 weeks.*Take 2 days off when taking S4 (repeat the cycle after the 2 day break) to avoid vision side effects.For RecompingUse S4 with a more anabolic SARM such as Ostarine for better recomp results as you’re aiming to gain muscle while losing fat. Recommended intake is 50-75 mg for 4 to 8 weeks.For BulkingS-4 isn’t the sarm that comes to mind when we think “BULKING”, but it’s properties in muscle gain shouldn’t be overlooked. During the holiday season, many people take advantage of the excess food and snacks available and jump on some well known bulking SARMs such as LGD 4033 or RAD 140. While there isn’t an enormous 15 lb leap in muscle like these “bulk specific” products, S-4 can provide relatively large muscle gains and utilize these excess calories to provide an extra 8-10 lbs in muscle while also keeping the body relatively lean. This steady increase in muscle mass can limit the amount of work one needs to do for a leaner summer body.The Benefits of S4 over Steroids

  1. Very minimal growth on secondary sexual organs such as the prostate.
  2. The LDL/ HDL ratio is not affected which makes it a low cardiovascular risk.
  3. 0% chance of aromatization, male breast lactation, or rise in any other female characteristic during the post cycle recovery.
  4. Testosterone is not diminished in any capacity during the post cycle recovery.
  5. Very exclusive in tissue selection and growth which means it will not cause heart enlargement or damage to neighboring organs.
  6. SARMs do NOT require the utilization or devouring of liver enzymes to activate their anabolic effects. This eliminates any risk of hepatotoxicity or hepatitis.
  7. 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.
  8. SARMs is very female friendly and does not cause excessive masculine features such enlarged sexual characteristics.
  9. S-4 has overall presented larger increases in muscle mass than DHT.

S4 Side Effects

Unfortunately, S-4 isn’t the perfect anabolic chemical and does come with some down sides. The first and possibly the most disappointing is that it follows the law of diminishing returns. Unlike anabolic steroids, sarms will become continuously less effective after a certain milligram percentage. For the average person it ranges from 50mg to 75mg. there are people that can go above this range for even more amazing results or need to stay below this range because they are unable to tolerate the chemical. About 99.5% of the population should fall within the 50mg to 75mg range.The most popular negative effects of S-4 are visual issues such as the yellow tint and difficulty adjusting to night vision. These side effects are unique to S-4 and are sometimes overblown. If these side effects present themselves, simply stop taking S-4 for two days and stay at a 5 day on/ 2 day off cycle. THESE EFFECTS ARE NOT PERMANENT! Once a ligand (such as a SARM) leaves the system, it’s effects disappear completely.Lastly, S-4 and most other SARMs have been known to cause depression in a small population of people. This has been discovered as more of a psychological issue than a physiological issue. researchers with mice suffering from any emotional disorders need to be cautious when using this chemical.REFERENCES Narayanan, R., Mohler, M. L., Bohl, C. E., Miller, D. D., & Dalton, J. T. (2008). Selective androgen receptor modulators in preclinical and clinical development. Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2602589/ Kim, J., Chen, J., & Dalton, J. T. (2005). Discovery and therapeutic promise of selective androgen receptor modulators. Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pubmed/15994457 Selective androgen receptor modulator treatment improves muscle strength and body composition and prevents bone loss in orchidectomized rats. (2005). Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pubmed/16099859 Dayger, C., Villasana, L., Pfankuch, T., Davis, M., & Raber, J. (2011). Effects of the SARM ACP-105 on rotorod performance and cued fear conditioning in sham-irradiated and irradiated female mice. Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048897/ Otto-Duessel, M., He, M., Adamson, T. W., & Jones, J. O. (2013). Enhanced Evaluation of Selective Androgen Receptor Modulators In Vivo. Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910424/ Effects of selective androgen receptor modulator (SARM) treatment in osteopenic female rats. (2009). Retrieved September 27, 2016, from https://www.ncbi.nlm.nih.gov/pubmed/19728047