S-23 SARM For Sale 10MG

Description

Sarmsamerica produces S-23 for sale with the highest quality and potency available. In animal research studies, S-23 demonstrated a half-life of 11.9 hours, with 96% absorption. Peak levels of the SARM were observed approximately four hours after administration. S-23 functions by binding to androgen receptor proteins, thereby activating muscle building within the body. While no human studies are available, a rat study reported that S-23 could prevent muscle loss via glucocorticoid receptors.

S-23 – What Should You Know

S23 is a selective androgen receptor modulator (SARM) known for its strong binding affinity to androgen receptors, surpassing other compounds like Andarine. Developed by GTx, Inc., a pharmaceutical company specializing in SARMs and SERMs, S23 demonstrates significant efficacy. GTx, initially founded as Genotherapeutics in Memphis in 1997, rebranded to its current name in 2001.

What is S23?

As mentioned, SARMs are selective in their action, aiming to mimic testosterone by binding to specific receptors in the body. S23 follows this mechanism, targeting bone and muscle tissue like other SARMs. It is considered one of the most potent SARMs available due to its strong bonding capability with androgen receptors. This binding enhances the activity of muscle-building proteins, leading to increased muscle mass for the user.

S-23 SARM: A Potent Nonsteroidal Selective Androgen Receptor Modulator

S-23 SARM is a nonsteroidal selective androgen receptor modulator, highly regarded in anecdotal reports and noted for its strong binding affinity to the androgen receptor, making it one of the most potent SARMs available, nearly as powerful as anabolic steroids. It is being studied for its effects on lean muscle gains, bone density, fat loss, sex drive, and as a potential oral male contraceptive.

S-23 Mechanism of Action

S23 mimics the action of testosterone in muscles and bones, potentially stimulating protein synthesis and muscle growth. As a relatively new SARM, S23 has never been clinically tested in mammals, so its safety profile has not been established. Studies on SARMs suggest that S23 may induce liver damage, affect fertility, and reduce natural testosterone levels in males.

Potential Male Contraceptive Agent

S-23 is currently being researched as a potential male contraceptive agent in rats. In a study, it caused temporary fertility interruption in all tested specimens. While this effect was reversible in rats, it’s important to note that S23 has never been tested in mammals, so it is unknown whether it interrupts fertility temporarily, permanently, or not at all in humans. Although S-23 SARM has high oral bioavailability, the rats in this study were injected with S23.

Effects on Lean Muscle Mass and Body Fat

This study also found that S23 increased lean muscle mass and decreased body fat in a dose-dependent manner, effectively countering the catabolic effects of estradiol benzoate administration. Another rat study showed that S23 prevented muscle loss in both fast-twitch and slow-twitch fibers due to glucocorticoids, indicating that it may have significant anabolic effects.

Research Demonstrated Increased Bone Mineral Density

The rat model also demonstrates an increase in bone mineral density from S23 SARM administration. Low quantities appeared to work equally well to high quantities. Bone mineral density increases are fairly commonplace with the administration of SARMs however S23 may be particularly effective in this regard.

Research has Shown Sexual Activity and Drive in Postmenopausal Female Rats

The rat model also demonstrated an increase in bone mineral density with S-23 SARM administration, with low doses appearing to be as effective as high doses. While bone mineral density increases are common with SARMs, S23 may be particularly effective in this regard.

A study on postmenopausal female rats showed that most SARMs could increase sexual activity and drive, with S-23 causing the most significant increase in sexual motivation without inducing growth in the uterus and uterine lining. However, males may experience the opposite effect due to S23’s tendency to reduce natural testosterone levels and its higher binding affinity for the androgen receptor.

Research has Shown Sexual Activity and Drive in Postmenopausal Female Rats

A research study on postmenopausal female rats revealed that many SARMs significantly boosted sexual activity and drive. Among them, S-23 stood out, showing the greatest enhancement in sexual motivation while not causing growth in the uterus or its lining. In contrast, male subjects might experience adverse effects, as S23 is known to lower natural testosterone levels and has a stronger binding affinity for the androgen receptor.

Scientific Insights Into S-23

A study conducted on rats demonstrated that S23 effectively reduced body weight and fat mass in the subjects. Additionally, estrogen was administered to promote mating, which initially led to a loss of muscle mass. However, S23 counteracted the estrogen’s effects, resulting in increased lean muscle mass. The fat reduction benefits of S23 are dose-dependent, with higher doses yielding better results.

Another study focused on glucocorticoid receptors, which transmit signals for substances like cortisol. In this study, S23 successfully prevented muscle loss in rats caused by glucocorticoids.

It’s not just about muscle; bones can be positively affected too. In other animal studies, S23 increased bone mineral density, a benefit commonly observed with many other SARMs.

Interestingly, S23 is also being researched as a potential male birth control option. However, this doesn’t mean you will permanently lose your ability to have children. Similar to how female birth control pills work, S23 reduces hormones like LH and FSH, which suppresses sperm production. Once you stop using it, your hormone levels generally return to normal, and fertility is restored.

A final benefit of S23 is its potential to boost sexual desire in women. In a study involving postmenopausal female rats, S23 increased sexual desire while maintaining the size of the uterus and uterine lining.

Side Effects of S23

The side effects of S23 are still under investigation, but some common ones include night sweats, cramping, increased aggression, acne, and the possibility of hair loss. Fortunately, many of these side effects are mild and often diminish over time.

S-23 Measurement Guidelines for Laboratory Use

Studies shows for higher gains, the dosage protocol for S23 is straightforward. Typically, dosages range from 10mg to 30mg. It’s recommended to start at the lower end to observe how the body reacts, then gradually increase the dose without exceeding 30mg. There are currently two variations of cycles commonly used.

S-23 in Experimental Studies on Fat and Muscle Balance

Unlike most other SARMs, which typically have an eight-week cycle length, S23 can be taken for up to twelve weeks and usually involves a post-cycle therapy (PCT) afterward. For bulking, the initial weeks involve taking 10mg per day to acclimate your body to the compound. Once accustomed, you can increase the dose to 30mg per day, divided into two or three doses. This could mean either three doses of 10mg or two doses of 15mg each day.

If you end your cycle at the eight-week mark, a PCT may not be necessary. However, if you extend to the full 12 weeks, it’s recommended to complete a PCT using both Clomiphene Citrate and Tamoxifen Citrate. For the PCT, Tamoxifen Citrate should be taken at 20mg per day, and Clomiphene Citrate at 25mg per day.

MK-677 is commonly stacked with S23 for those looking to enhance performance and boost muscle bulk. This combination can maximize the benefits, providing significant improvements in muscle growth and overall physical performance.

For cutting, the dosage protocol for S23 remains the same as for stacking. The main difference is maintaining a calorie deficit. If you want to enhance your cutting cycle further, you can stack S23 with GW501516, MK2866, or S4 instead of MK-677. Regardless of the stacking choice, it’s essential to complete at least a two-week PCT afterward.

S-23 SARM Molecule

Data on our S-23 for sale

This preparation is strictly for laboratory research purposes and has not been approved by the FDA for human consumption. S23 is NOT a dietary or sports supplement.

S23 SARM FAQs

What does S-23 SARM do?

S23 works by selectively binding to androgen receptors, specifically targeting tissues such as muscle and bone. This selective binding triggers processes that promote muscle growth, increase bone density, and aid in fat loss, without significantly impacting other organs like the liver or cardiovascular system.

Is S-23 a male contraceptive?

S-23 is an investigational selective androgen receptor modulator (SARM) developed by GTX, Inc. It is being researched as a potential male hormonal contraceptive.

Is S23 the best SARM?

S23 is undoubtedly one of the most potent SARMs currently in development. It boasts an extremely high binding affinity, is highly suppressive, and is a very effective muscle builder with a high level of tissue selectivity compared to anabolic androgenic steroids.

Does S23 lower testosterone?

Data suggests that S23 may temporarily but significantly lower natural testosterone levels in males.

Why buy S23 SARM from Sarmsamerica?

If you’re looking where to buy S23 online, widely regarded as the strongest SARM, you’ll find many options. However, not all companies offering S23 for sale are reliable or trustworthy. Purchasing capsules S23 from a randomly selected pharmaceutical company or website can be dangerous, even if the price seems reasonable, due to uncertain quality-control processes.

Sarmsamerica is the best place to buy S23 online due to our consistent, verifiable high-quality products, safer bottling and packaging, fast shipping, and excellent customer service.

When you buy SARMs like S23 from Sarmsamerica, you’re choosing the highest quality ingredients. Our compounds are a minimum of 98% pure, tested, and certified by accredited American third-party labs. They are suspended in USP grade (the highest grade) PEG400 and bottled in America. Our products are packaged in glass bottles with fixed glass droppers to prevent the leaching of unwanted plasticizers like BPA and to avoid contamination from external measuring tools.

At Sarmsamerica, we run a transparent business with no need for discreet payment methods and no misrepresentation of our products. We offer only the highest quality research chemicals available online. We provide free USPS shipping on orders over $160, and for those needing products quickly, we offer express shipping options. Additionally, customers who sign up for our email list receive a 10% discount.

That’s why we’re confident in our claim that we offer the best S23 for sale on the market today. If you have any questions about our capsules S23 products, feel free to contact us, and we’ll respond as soon as possible.

Abuse Warning

S23 is an investigational compound still awaiting FDA approval and is not a dietary supplement. At Sarmsamerica, we are chemical suppliers, not medical doctors, and our expertise lies in sourcing and quality control. We do not encourage or condone consumer use of SARMs products; they are strictly for research purposes only.

SARMs should only be used under the supervision and direction of a medical doctor or designated research authority. We strongly discourage the use of SARMs for performance enhancement in sports and bodybuilding and warn against relying on “bro science” and peer consensus when making decisions about human health.

Scientific References:

1. Jones, A., Chen, J., Hwang, D. J., Miller, D. D., & Dalton, J. T. (2009). Preclinical characterization of a (S)-N-(4-cyano-3-trifluoromethyl-phenyl)-3-(3-fluoro, 4-chlorophenoxy)-2-hydroxy-2-methyl-propanamide: a selective androgen receptor modulator for hormonal male contraception. Endocrinology, 150(1), 385–395.
2. Jones A, Hwang DJ, Narayanan R, Miller DD, Dalton JT. Effects of a novel selective androgen receptor modulator on dexamethasone-induced and hypogonadism-induced muscle atrophy. Endocrinology. 2010 Aug;151(8):3706-19. doi: 10.1210/en.2010-0150. Epub 2010Jun 9. PMID: 20534726.
3. Jones, A., Hwang, D. J., Duke, C. B., 3rd, He, Y., Siddam, A., Miller, D. D., & Dalton, J. T. (2010). Nonsteroidal selective androgen receptor modulators enhance female sexual motivation. The Journal of pharmacology and experimental therapeutics, 334(2), 439–448.
4. https://academic.oup.com/endo/article/150/1/385/2455919?login=true
5. https://jpet.aspetjournals.org/content/334/2/439.short
6. https://academic.oup.com/endo/article/151/8/3706/2456888?login=true
7. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630904/