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Product Details:
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| Product Name: | Andarine (GTX-007) | CAS: | 401900-40-1 |
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| Assay: | 99.6% | Policy: | Reshipping Policy |
| Packing: | As You Required | Delivery: | 5-7 Working Days |
| Shipment: | EMS, HKEMS, DHL, FEDEX, EUB | Description: | Yellow Powder |
| High Light: | steroids raw powder,pharmaceutical anabolic steroids |
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Andarine Gtx -007 Sarms Source Yellow Powder for Bodybuilding
Product name:Andarine (GTX-007)
S4 Andarine CAS:401900-40-1
S4 Andarine Apperence:White powder
S4 Andarine Assay:99%
S4 Andarine Formula C19H18F3N3O6
S4 Andarine Molecular mass 441.357 g/mol
S4 Andarine Storage: at 20ºC 2 years
Andarine(S4) Description:
Andarine (GTx-007, S-4) is an investigational selective androgen receptor modulator (SARM) developed by GTX, Inc for treatment of conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy,[1] using the non-steroidal androgen antagonist bicalutamide as a lead compound.
Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.[3] This suggests that it is able to competitively block binding of dihydrotestosterone to its receptor targets in the prostate gland, but its partial agonist effects at androgen receptors prevent the side effects associated with the anti-androgenic drugs traditionally used for treatment of BPH.
Dosing of S4 Andarine;
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 vision.
S-4 (3 mg/kg/day) was also able to restore skeletal muscle (i.e., soleus muscle) and strength in castrated rats, important and applicable for the treatment of muscle wasting and male HRT.
A 120-day study comparing SARM S-4 and dihydrotestosterone (DHT) treatment in ovariectomized rats demonstrated that S-4 was able to maintain bone mass and bone strength to the levels of intact controls and exhibited greater efficacy than DHT.
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