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S4 is often a form of SARM that attaches towards the androgen receptor (AR) exactly the same with regular androgens, the sole variation is always that S4 generates selective anabolic activity. S4 is a SARM with utmost androgenic effects mainly because it around 33% in the strength of testosterone when attaching to AR.
When compared with given and prohormones, Andarine won't have androgenic activity in non-skeletal muscle tissues
S4 is often a SARM with maximum potential which has a disintegration procedure for just 4 hours. It may reduce the height and width of the prostate if taken as recommended. It can be administered orally.
It's proved to be very theraputic for muscle degeneration, osteoporosis and benign prostatic hypertrophy (with bicalutamide - a non-steroidal androgen antagonist) treatment. Aside from preserving muscle mass, S4 could also help improve it.
Apart from its muscle mass building advantages, S4 won't cause liver damage, can prevent gynecomastia (enlarged breasts of males) which enable it to help supercharge your all around health.
SARMS including S4 can cause muscle increase in the identical manner as steroids, however unlike testosterone and also other steroids, SARMS (as nonsteroidal agents) tend not to produce the growth impact on prostate along with other secondary sexual organs.
SARMS not just represent a fresh potential treatment alternative for an extensive spectrum of conditions including muscle wasting diseases (from age-related to AIDS or cancer-related), but they also have immense risk of muscle development for Bodybuilders, fitness and athletes.
Andarine is an orally active partial agonist for androgen receptors. It's less potent in the anabolic and androgenic effects than other SARMs. In a animal label of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with the exact same efficacy to finasteride, but without producing any decline in muscular mass or anti-androgenic negative effects.
This implies that it is capable of competitively block binding of dihydrotestosterone to the receptor targets inside the men's prostate, however its partial agonist effects at androgen receptors steer clear of the side effects associated with the anti-androgenic drugs traditionally utilized for management of BPH.
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Certificate Of Analysis
|Batch No.||20180806||Expiry date||2 years|
|Test standard||In-house quality standard|
|Conclusion:The product meets In-house specifications.|
|Issued by:Xiaokang Ma||Checked by:Feng Yuan||Analyst:Peng He|
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