Pharmacological effect
Oxyhydroloon is a structurally altered dioxytestosterone hormone. It is A form of dioxytestosterone in which the 2-carbon atom in the A-carbon ring is structurally replaced by an excess oxygen atom. This structural change greatly enhances its anabolic capacity and prevents it from being metabolically broken down. In addition, the 17 carbon atoms on the molecule are replaced by a methyl group, forcing it to become a C17 anabolic steroid that can be taken orally. Since Xylene does not aromatize, any muscle gain from using Xylene is fat free. It also does not cause water storage. However, in the combination cycle of the muscle-building steroid CYCIE, oxyhydroloon should not be used as the primary drug class in the cycle, but should be used in combination with testosterone Norone injections. Users can gain some pure muscle mass, and the muscle gained by using oxyhydroxy is easier to retain. In particular, during the muscle-building cycle, users value the potential for pure muscle growth in the body, which allows users to gain less body fat during the off-season. Because of the increase in free testosterone in the body caused by oxyhydroxone, most users will find that other steroids work better when combined. The use time of oxyhydrogen dragon in the fat reduction period is the best, but also can maximize the role of oxymale dragon. Due to its strong anabolic capacity, xanthohydrone is one of the best compounds to conserve muscle during the fat loss phase, which increases muscle firmness. [1]
Usage and dosage
Methanolone can be rapidly absorbed through gastrointestinal administration, and its metabolites and unaltered methanolone are excreted primarily through the kidney and to a lesser extent through the intestine. Generally oral 2.5 ~ 20mg/d. For the treatment of growth and puberty delay in boys, oral 1.25 ~ 2.5mg/d or 0.25mg/kg should be taken for a short course of treatment, usually 3-4 months, to prevent the closure of epiphysis. Turners syndrome in girls, 0.05 ~ 0.125mg/ (kg·d) orally. [2]
Precautions for use
Oxyhydrolonone is an androgen active drug molecule, which may cause jaundice and other adverse reactions if the patient takes it for a long time. As a C-17 anabolic steroid, methohydroxone is the least hepatotoxic of all C-17 steroids. The therapeutic dose of oxyandroxone did not significantly increase the enzyme levels in the liver. Of course, drug use has a greater impact as a performance enhancer. It is important to note that the increase in liver enzymes does not directly cause liver damage, but long-term exposure to this type of stress can lead to liver injury. So try to use liver tablets in circulation. One is to protect the liver and two is to make the drug work better. All steroid use suppresses the body's own testosterone production. However, the inhibitory effectiveness of different steroids varies. The inhibitory effect of oxyhydrolon is very weak, and the side effect of suppressing testosterone can be controlled by using oxyhydrolon. Even in high doses, oxyandrogen can cause at most a 50% decrease in testosterone levels, which is still an acceptable range for some men. A lot of it has to do with your own testosterone levels, so if you have low testosterone levels, you're going to have to add testosterone and other drugs to your circulation. [2]
