M1T, or methyl-1-testosterone, also known as methyl dihydroboldenone derivative, does not aromatize or cause water retention, eliminating the need to consider estrogenic side effects. However, it is highly hepatotoxic. It effectively increases lean mass and muscle quality, making it suitable for use during cutting or competition preparation phases.

Description:

M1T originated from boldenone, which itself evolved from Dianabol by eliminating the hepatotoxicity of Dianabol. Boldenone, after undergoing 5-alpha-reduction, becomes dihydroboldenone, also known as 1T. 1T is then transformed into the orally active methyl-1-testosterone, M1T, through 17-alpha-methylation. Developed in 1962 using molecular engineering techniques, M1T boasts incredible and formidable strength. Compared to testosterone (100:100), M1T's anabolic potential is an astonishing 900-1600, while its androgenic rating is only 100-200. Its potent protein-synthesizing ability and minimal increase in androgenic properties enable it to produce optimal muscle synthesis effects. Originally developed to circumvent drug regulation laws, M1T was categorized as a "dietary supplement" and included in various sports nutrition products, allowing a broad audience to experience its muscle-building benefits. However, once regulatory bodies recognized M1T's true nature as an anabolic steroid, it was classified as a controlled substance.

When thinking about anabolic steroids, the darker aspects of competitive sports often come to mind. However, less known is that during the mid-20th century, hundreds of well-known pharmaceutical companies were intensely developing these mysterious substances night and day. M1T was one of their research subjects. Despite the hundreds of drugs awaiting approval each year, M1T ultimately did not receive authorization. Yet, approval merely grants a drug a legal status; an unapproved drug, despite lacking regulatory recognition, can still outperform many classic anabolic steroids.

The strength of M1T lies in its ability to increase effective body weight by 15-20 pounds within just 2-4 weeks of low-dose use. It can be used alone or in conjunction with injectables for maximum effect. Given the potential visceral stress caused by M1T, its continuous use is generally not recommended beyond six weeks.

Unlike Dianabol or Anadrol, the weight and strength gains from M1T are solid: M1T does not aromatize, thus it absolutely will not cause water retention. For customers seeking rapid, high-quality weight gain, M1T is an unmissable option. M1T is the Midas touch, as well as the key to unlocking dark powers. It unleashes your full potential, allowing you to enjoy the thrill of training, comprehensive improvement, and dominating your competition.

Structural Features:

M1T is derived from boldenone after a 5-alpha-reduction to dihydroboldenone (1T), which is then 17-alpha-methylated to become the orally active Methyl-1-Testosterone, M1T. M1T does not aromatize in the body, and no estrogenic activity has been detected. Therefore, anti-estrogens are unnecessary, as gynecomastia will not be a concern in sensitive individuals. As estrogen is a common cause of water retention, this steroid produces a lean mass appearance without excessive subcutaneous fluid retention. This makes it beneficial during cutting cycles when water and fat retention are major concerns.

Androgenic Side Effects:

M1T is classified as an androgen. Common androgenic side effects include oily skin and may necessitate the use of milder, less androgenic steroids. As a potent androgen, this steroid can also increase aggression. Women are cautioned that androgenic/anabolic steroids pose a potential for severe adverse effects, including deepening of the voice, irregular menstrual cycles, changes in skin texture, facial hair growth, and clitoral enlargement.

Estrogenic Side Effects:

M1T does not aromatize, and no estrogenic activity has been detected. Using this steroid does not require anti-estrogens, as gynecomastia is not a concern among sensitive individuals. As estrogen commonly causes water retention, this steroid can produce a lean appearance without excessive subcutaneous fluid retention, making it beneficial for cutting cycles.

Hepatotoxicity:

M1T is a c17-alpha alkylated compound. This modification protects the drug from deactivation by the liver, allowing a high proportion of the drug to enter the bloodstream after oral administration. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Long-term or high-dose use can lead to liver damage. It is recommended to regularly visit a physician to monitor liver function and overall health during each cycle. The intake of c17-alpha alkylated steroids is usually limited to 6-8 weeks to avoid elevated liver strain. A study involving a group of nine male subjects taking 20 mg of fluoxymesterone for two weeks showed that the majority of participants (6/9) noted abnormal bromsulphalein retention, a marker of liver stress. When taking any hepatotoxic anabolic/androgenic steroid, it is advisable to use liver detoxification supplements such as Liver Stabil, Liv-52, or Essentiale Forte.

Cardiovascular Effects:

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes tendencies to lower HDL (good) cholesterol values and raise LDL (bad) cholesterol values, which may shift the HDL to LDL balance, thus increasing the risk of arteriosclerosis. The relative impact of anabolic/androgenic steroids on serum lipids depends on the dose, the route of administration (oral vs. injectable), the type of steroid (aromatizable or non-aromatizable), and the level of resistance to hepatic metabolism. Fluoxymesterone's structural resistance to liver cholesterol and its mode of administration significantly affect liver cholesterol. Anabolic/androgenic steroids can also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and cause ventricular hypertrophy, potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oil (4 grams per day) and natural cholesterol/antioxidant formulas like Lipid Stabil or similar ingredients is also recommended.

Testosterone Suppression:

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production when taken in doses sufficient to promote muscle gain. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Prolonged hypogonadotropic hypogonadism can develop secondary to steroid abuse, requiring medical intervention.

Usage:

Studies have shown that simultaneous intake of oral anabolic steroids with food can decrease their bioavailability. This is due to the fat-soluble nature of steroid hormones, which may cause some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization, this type of steroid should be taken on an empty stomach.

Treatment (Men):

Athletes are generally advised to take a dose of 10 mg, and warnings are given not to attempt doses above 10 mg without caution.

Use (Women):

M1T is not recommended for physique or performance enhancement purposes in women.

Prev: Dianabol

Next: Fluoxymesterone

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