Methandriol Dipropionate Prohormone Steroids Powder for Muscles Building 3593-85-9
Appearance: White powder
Standard Testosterone propionate
Chemical Name 17-alpha-methylandrost-5-ene-3,17-beta-diol
Estrogenic Activity low to moderate
Methylandrostendiol is a modified form of dihydrotestosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha to protect the hormone during oral administration and 2) the introduction of a double bond between carbons 5 and 6, which seems to increase the anabolic strength of the steroid (partly by making it resistant to metabolism by 3-hydroxysteroid dehydrogenase in skeletal muscle tissue). Methylandrostenediol dipropionate contains methylandrostenediol modified with the addition of 2 carboxylic acid esters (propionic acid) at the 3-beta and 17-beta hydroxyl groups, which delay the release of free methylandrostenediol from the site of injection (depot).
The usual dosage for athletes is 100 mg every 2-3 days. In Europe only the oral form of M.D. is available. Also in this case it is beneficial to combine M.D. with another steroid, preferably an injectable one. The normal daily dose is 40-60 mg and is usually taken in 2-3 individual doses spread over & day The tablets are usually taken for only 4-6 weeks since the effect decreases quickly, thus requiring higher dosages. They are also I 7-alpha alkylated so even a low dos-age and a short intake can be damaging to the liver. Because of its androgenic effect women rarely use M.D. Possible side effects of the tablet form can be elevated levels of liver toxins, gastrointestinal pain, acne, gynecomastia, increased aggressiveness, and high blood pressure.
Stacking and Use:
Methandriol is mostly found as a 17-alpha-alkylated oral, meaning the time-span of its use is limited due to hepatoxicity. After a stack with such a compound one might want to stack a number of proven liver protectors such as P450, milk thistle and Vitamin B6. The reason I do not recommend you take them while taking an oral methylated or ethylated steroid is because they obviously fortify the liver and may increase the hepatic breakdown of your oral compounds. Secondary drugs with methandriol are not wishful. Its not a strong androgen of its own, and most of its anabolic effects are mediated by agonizing estrogen. So while stacking an anti-aromatase or estrogen antagonist may help relieve estrogen-related conditions, it also totally negates any use you may have for this substance.
One would preferably stack this with an aromatizable compound is the logical conclusion. Testosterone (250-750 mg per week) being the prime candidate since it aromatizes well allowing the methandriol to execute its primary function, and is adequately androgenic through its conversion at the 5-alpha-reductase enzyme (to form DHT) that it can benefit from methandriols ability to upgrade the androgen receptor. Those who fear estrogenic effects, may prefer a mildly aromatizing hormone such as boldenone (300-400 mg per week) better, though one has to wonder about the use of a moderate compound like boldenone by itself, since the methandriol has no real addition of its own to make.
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