Drostanolone Propionate is anabolic (known as dromostanolone) is a modified dihydrotestosterone. It differs by the addition of a methyl group at position 2alpha that affects the increase in strength anabolic steroid, increasing resistance to metabolism by the enzyme 3A-hydroxysteroid by in muscle tissues (2alpha,5alpha,17 beta)-17-Hydroxy-2-methylandrostan-3-one formula C20H32O2. The drostanolone propionate is a modified form of drostanolone, with attached propionate ester in 17-beta hydroxyl group. In contrast to free steroids, esterified less polar, and therefore not absorbed as quickly from the injection site. Once in the bloodstream, the ester is cleaved and the blood moves freely drostanolone. Develop esterified steroids was to increase the period of therapeutic effect after entering, to make the injections less frequently, when compared with receiving free steroids. Period half-life of drostanolone propionate is approximately two days after injection. In the medical literature drostanolone describe as a powerful anabolic anti-estrogenic properties. Despite this, many scientists recognize that the anabolic properties of Grotanol rather moderate when compared with similar drugs. Widely used by athletes who are dieting, and is also involved in speed and power sports, in which its property to influence the increase of muscle mass and strength, reducing body fat, while having no serious side qualities.
Drostanolone Propionate reduces the production of luteotropic and follicular stimulating hormones. Drostanolone Propionate has an androgenic (when compared with testosterone propionatom, it is expressed less) and anabolic (expressed more than testosterone propionate) action. Has antitumor effects in patients with cancer of the thymus gland, even in the presence of metastases, and in patients with suppressed ovarian function in connection with radiation, androgen drugs or subjected to ovariectomy.The effect is greater when performing a bilateral ovariectomy. Has an anabolic effect, this is expressed in the stimulation of protein synthesis, decreasing fat deposits, delayed in the human body necessary for the synthesis of protein, potassium, phosphorus, sulfur, enhancing fixation of calcium in the bones and increasing muscle mass. In the presence of adequate protein nutrition stimulates the production of erythropoietin.
The recommended dose of the drug is equal to 300-500 mg/ 7 days, usually on the third day, or one one. Course duration 6(8)-10(12) weeks. Usually combined with nandrolone decanoate or boldenone undecylenate, it affects the increase of muscle tissue, while not unduly delaying the water. In order weight gain combine it with an injectable testosterone, it affects the growth of muscle mass without a surplus of “water”, which would have accumulated if taken with other drugs. Drostanolone Propionate is used in order to “drying”. Combine it with other non-aromatizing drugs, for example, stanozolol, Primobolan, trenbolone or Oxandrolone, and it helps to keep muscle on a diet and losing.
Drostanolone does not aromatize and does not have estrogenic activity. Anti-estrogen is not needed, even sensitive people will not notice the existence of gynecomastia. As a rule, estrogen retains water, but taking this steroid increases quality weight without excess fluid. In this regard, the drug is good to use for “drying”, that’s when the main problem is water retention and fat. As a non-aromatizing derivative of dihydrotestosterone, drostanolone may be some anti estrogenic effect, thus competing with other agents for binding with aromatase.
Despite the fact that drostanolone propionate is classified as an anabolic, androgenic side effects may be present. High doses of the drug can cause increased oiliness of skin, pimples, hair growth on the body and face. Anabolic steroids are likely to worsen the hair loss in males. Women should be reminded about possible Vasilissa the AAS effects (coarsening of the voice, irregular periods, change in the structure of the skin, hair growth on the face and increase of the clitoris). Drostanolone does not react with 5A-reductase and androgenetic not be possible to change concurrent use of finasteride or dutasteride. Despite the fact that this steroid with a low androgenic activity, a threshold of its androgenic side effects much more than testosterone, methandrostenolone, and fluoxymesterone.