CORE LABS M-DROL (SUPERDROL)

CORE LABS M-DROL (SUPERDROL) Synonyms: Methyldrostanolone, Methasterone, M-Drol, S-Drol, Methastadrol. Pharmaceutical nomenclature: 2a,17a-dimethyl-5a-androst-3-one-17b-ol 2a,17a-dimethyl-etiocholan-3-one-17b-ol Characteristics of Superdrol: Androgenic activity: 20 Anabolic activity: 400 Standard: Methyltestosterone (oral) Chemical name: 2a, 17a-dimethyl-Sa-androstan-17b-ol-3-one Estrogenic activity: none Progestational activity: low What is Superdrol? Methyldrostanolone (Superdrol) is a modified form of dihydrotestosterone. It differs: 1) by adding methyl groups at carbon 17-alpha, which helps protect the hormone when taken orally, and 2) by introducing a methyl group at carbon-2 (alpha), which significantly increases the anabolic strength of the steroid by increasing its resistance to metabolism by 3-hydroxysteroid dehydrogenase enzymes in skeletal muscle tissue. Side effects of Superdrol: Estrogenic. Methyldrostanolone is not an aromatizable substance in the human body, and does not exhibit noticeable estrogenic effects. The use of anti-estrogens is not mandatory when using this steroid, and gynecomastia should not occur even in sensitive individuals. Estrogen usually affects water retention in the body, while Methyldrostanolone produces a quality appearance without excess fluid retention. This makes it a favorable steroid for use during cutting cycles, when water and fat retention are major concerns. Androgenic. Although the steroid is classified as an anabolic, androgenic side effects when using this substance are quite common and may include oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids can also exacerbate male pattern baldness. Women should be warned about the potential virilizing effects of anabolic/androgenic steroids. These may include deepening of the voice, menstrual cycle disturbances, changes in skin texture, facial hair growth, and clitoral enlargement. Methyldrostanolone is a steroid with relatively low androgenic relative activity, making the threshold for strong androgenic side effects relatively higher than when using more androgenic substances such as testosterone, methandrostenolone, or fluoxymesterone. Note that Methyldrostanolone is not affected by the 5-alpha-reductase enzyme, so the relative androgenicity of the substance is not dependent on concurrent use of finasteride or dutasteride. Hepatotoxicity. Methyldrostanolone is a c17-alpha alkylated compound. This protects the drug from deactivation in the liver, allowing a very high percentage of the drug to enter the bloodstream after oral administration. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged exposure or high dosages can cause liver damage. It is advisable to visit a doctor periodically during each cycle to monitor liver function and overall health. The use of c17-alpha-alkylated steroids is usually limited to 6-8 weeks to avoid escalating liver strains. Although there is no data to make such statements, results from private laboratory tests show that doses of 10 mg and 20 mg per day are sufficient to increase liver enzyme levels in consumers. In addition, a small number of serious adverse events related to liver toxicity have been reported with the use of this substance. When using any hepatotoxic anabolic/androgenic steroids, it is recommended to take liver detoxification supplements. Cardiovascular system. Anabolic/androgenic drugs can have a detrimental effect on cholesterol levels. This includes tendencies to lower HDL (good cholesterol) and raise LDL (bad cholesterol), which can contribute to the risk of atherosclerosis. The degree of impact of anabolic/androgenic drugs on blood serum lipids depends on dosage, route of administration (oral or injectable), type of steroids (aromatized or not), and level of resistance to liver metabolism. Methyldrostanolone has a strong influence on cholesterol levels in the liver because the substance is non-aromatizable and, due to its structure, is able to resist breakdown in the liver. Anabolic/androgenic steroids can also negatively affect blood pressure and triglyceride levels, reduce endothelial relaxation, and contribute to left ventricular hypertrophy, all of which potentially increase the risk of cardiovascular diseases and myocardial infarction. To reduce the risk of cardiovascular deformities, it is recommended to perform active exercises and minimize the consumption of saturated fats, cholesterol, and simple carbohydrates throughout the entire period of active AAS (anabolic/androgenic steroids) use. It is also recommended to take additional omega-3, vitamins, and antioxidants. Testosterone suppression. All anabolic/androgenic drugs, when taken in effective dosages sufficient to increase muscle mass, suppress the production of endogenous testosterone. Without intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months after discontinuing the drug. To reduce the likelihood of negative processes and shorten recovery time, take supportive and PCT (post-cycle therapy) drugs during and after the cycle. Application of Core Labs M-Drol. 1 capsule twice a day, during or immediately after a meal. Morning and evening. Daily. Maximum course of administration - 1 month. IMPORTANT! Taking supportive drugs during the course and PCT is mandatory! Показать полностью

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