Androx is famous because it was one of the first anabolic steroid where were a mix of 4 different testosterone esters. This preparation contains: testosterone propionate, testosterone isocaproate, testosterone phenylpropionate and testosterone decanoate. It was created for fast and at the same time long action. It is a strong anabolic steroid with well-expressed androgenic component. The active live of this anabolic is approximately 21 days. Once you started a cycle of 8-12 days of injecting, like one time during 5 days of Androx, it will give effective results. In the first 5 days, already you will notice an increase in your weight training. Bodybuilders are using Androx usually to put on mass and size while increasing the strength. Taking Androx even during the first cycle, it can bring very good results in the first cure, even if the dose isn’t so big. Because of its ability to absorb water, this preparation is not suitable for pre-competition preparation in bodybuilding. At the same time, being very a strong androgen, post course therapy should take place approximately 2 weeks after the last injection of the preparation, because it is active during long time in the blood. If you really need extreme volume, then you may combine Androx with Anadrol or Dianabol. But if you need for a clear relief, it could be combined with Trenbolone Mix or of Androx:· Increase of power rate· Increase of muscle mass· Increase of red blood cell formation· Increase of catabolic processes· Increase sexual desire during the cycle, and decline after its completionSpecification:· Active Life - 21 days· Average Dose - 250-1000 mg/weekly· Aromatization - Yes..
Anabolic androgenic steroids (AAS) were initially created for therapeutic purposes, and synthetic derivatives of the male hormone testosterone. Due its great anabolic effects, these drugs are being used on a large scale, for the improvement of sports performance. In this present study, we aim to show the history of it’ use, present their mechanisms of action, more particularly its use correlate with improved body composition, muscle mass, aerobic capacity and verify their possible side effects, analyzing their use therapeutic and indiscriminate, through direct scientific research with the sports. Sources were reviewed scientific the following search engines: PUBMED, LILACS and SCIELO. The results showed that in presence of a suitable AAS and diet can contribute to increases in body weight, particularly lean body mass and muscle strength gains achieved by high intensity exercise, these effects can be further potentiated, the use of supraphysiological doses, but in the aspect of aerobic power, there are not scientific evidence to support their improvement. Regarding side effects, the use of AAS, is related to several complications in the liver, cardiovascular system, reproductive system and psychological characteristics, always assigned by the non-therapeutic and abuse of AAS. Thus we conclude that the use of AAS, are directly linked to gains muscle mass, strength, as well several side effects, always assigned to abusive and indiscriminate doses, it is noteworthy that the scientific literature, still has a certain lack of studies, mainly randomized, controlled, with supraphysiological doses in human, so many effects are still unknown.
Hormone replacement therapy has been shown to have other beneficial effects. In a study women taking estrogen through HRT showed that the estrogen positively affects the prefrontal cortex by boosting the working memory. This suggests that estrogen may play a key role in certain frontal lobe functions in women.  Women using HRT after menopause have no additional weight gain compared to women who do not use HRT.  Also women who use HRT with an estrogen component show positive effects in their sex life (mainly increasing their sex drive and sexual sensitivity) but the effects are inconsistent across women. These sexual improvements may dissipate after receiving some forms of HRT for extended periods of time. 
DHT is a potent agonist of the AR, and is in fact the most potent known endogenous ligand of the receptor. It has an affinity (K d ) of to nM for the human AR, which is about 2- to 3-fold higher than that of testosterone (K d = to nM)  and 15–30 times higher than that of adrenal androgens .  In addition, the dissociation rate of DHT from the AR is 5-fold slower than that of testosterone.  The EC 50 of DHT for activation of the AR is nM, which is about 5-fold stronger than that of testosterone (EC 50 = nM).  In bioassays , DHT has been found to be - to 10-fold more potent than testosterone. 
DHT is a potent agonist of the AR, and is in fact the most potent known endogenous ligand of the receptor. It has an affinity (K d ) of to nM for the human AR, which is about 2- to 3-fold higher than that of testosterone (K d = to nM)  and 15–30 times higher than that of adrenal androgens .  In addition, the dissociation rate of DHT from the AR is 5-fold slower than that of testosterone.  The EC 50 of DHT for activation of the AR is nM, which is about 5-fold stronger than that of testosterone (EC 50 = nM).  In bioassays , DHT has been found to be - to 10-fold more potent than testosterone.