Trenbolone acetate – has a minimum duration of action (the short period of half-ruined), which is why the drug was injected daily in doses of about 50 mg (daily) or 100 mg (every other day) for the convenience and choice.
By the way, acetate is the most popular form of the drug.
Trenbolone has a high affinity for the androgen receptor, binding capacity exceeds 4.5 times that of testosterone. This is due to a high anabolic activity of the drug. Trenbolone is one of the most powerful steroids in their ability to increase strength gains and muscle mass. At the same time it is reflected in the frequency of side effects, the risk of which is quite high, especially in improperly formatted courses.
Trenbolone gained its popularity mainly because it is not able to be aromatized into estrogens under the influence of aromatase; for analysis, you may receive an opinion that it provokes the rise of estradiol in the blood (the effect is much smaller in Hexahydrobenzylcarbonate), but this is an error of judgment, because metabolites of testosterone assays may be referred to as estodiol. It does not deprive him of the side effects such as gynecomastia and fluid accumulation, which is mainly manifested expense progestin activity.
Trenbolone suppresses the production of testosterone, due to the feedback mechanism and progesterone activity (which may provoke the gynecomastia). This results in side effects such as decreased libido, erection and flaccid testicular atrophy.
Trenbolone is 19-nor derivatives of testosterone, which makes it similar to nandrolone against progestin activity. Trenbolone is able to bind to progesterone receptors, which in rare cases leads to gynecomastia, decreased libido (Deca-Dick), this property is not very pronounced.
Detection time – up to 5 months.