|Provides a huge increase in strength and weight in a short time||one of the most dangerous of oral steroids|
|Increases the synthesis and proteosynthesis and glycogenesis||risk of acne, hair loss, body hair growth|
|Accelerates the muscle regeneration||risk of gynecomastia|
|Strongest oral anabolic steroid||suppresses natural production of androgenic hormones|
|Causes an increase in the number of red blood cells||increased blood pressure due to excessive water retention in the body|
|resulting in excessive muscle pump effect||
CHEMICAL NAME: 9-fluoro-11,17-dihydroxy-10,13,17-trimethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
HALF RELEASE: 9.5 hours
Anabolic RATING: 1900
Androgenic RATING: 850
Fluoxymesterone is extremely powerful anabolic steroid, stronger than trenbolone, which is considered the most powerful anabolic steroid conventionally available.
Since fluoxymesterone is highly hepatotoxic, and has negative influences on cholesterol profile of blood in health it is only used to treat male androgen deficiency.Although for the same purposes testosterone represents a safer and simpler treatment, fluoxymesterone is today still available by prescription in the United States.
Fluoxymesterone has added methyl group at carbon 17 (hence the name derived from 17-alpha) and halo-group on the 9th carbon.Adding a methyl group at carbon 17 is the change that provides the hormone the ability to survive metabolism in the liver, and thus allow a greater amount of hormone to successfully get into the bloodstream. Unfortunately, this modification also increases the rate of hepatotoxicity (liver toxicity). Connecting halogen to any substance is called halogenation. In our case to the testosterone was attached with fluorine (halogenated).
The halogenation is responsible for the massive increase in androgen and anabolic forces of fluoxymesterone compared with testosterone and methyltestosterone.
Compared with testosterone fluoxymesterone has one more change and that is the attached hydroxyl group (an oxygen bonded to a hydrogen atom) on the 11th carbon.Connection of the hydroxyl group at carbon-11 accounts for the fluoxymesterone inability to react with enzyme aromatase and therefore preventing it conversion to estrogen.
Athletes take oxymetholone primarily as a "starter" substance at the beginning of the injection cycle, the effect of which is slow (e.g. with testosterone, nandrolone, methenolonom, boldenone). Separate use of oxymetholone does not make sense, because the results are hardly sustainable.