Testosterone esters were synthesized for the first time in 1936, and were found to have greatly improved potency relative to testosterone.  Among the esters synthesized, testosterone propionate was the most potent, and for this reason, was selected for further development, subsequently being marketed.  Testosterone propionate was introduced in 1937 by Schering AG in Germany under the brand name Testoviron.  It was the first ester of testosterone to be introduced,  and was the major form of testosterone used medically before 1960.  In the 1950s, longer-acting testosterone esters like testosterone enanthate and testosterone cypionate were introduced and superseded testosterone propionate.  Although rarely used nowadays due to its short duration,  testosterone propionate remains medically available. 
Anabolic steroids are synthetic versions of hormones that human body produces naturally. Their main role is to assure increased physical performance in all sports and athletic pursuits. Steroidal compounds enhance stamina, strength, weight and size of muscles and may improve the energy levels during physical training. Oral and injectable steroids posses the ability to increase athletic performance, have a positive effect on red blood cells production and bones density. The steroids are used in accordance with requirement and needs of any athlete individually. There are special compounds which are not suitable for women and a series of anti-estrogen products which main role is to counter the eventual side effects of steroids use and to restore natural testosterone levels of the human body. These compounds nowadays became an important part of muscle building process among professional athletes and bodybuilders, as well as regular people, males and females that have the goal to become more attractive and exhibit good looks. Follow us on Twitter | Steroids Store - Pinterest .
In androgen-responsive target tissues such as the skin, scalp, and prostate, the high relative androgenicity of testosterone is dependant on its reduction to dihydrotestosterone (DHT). The 5-alpha reductase enzyme is responsible for this metabolism of testosterone. The concurrent use of a 5-alpha reductase inhibitor such as finasteride or dutasteride will interfere with site-specific potentiation of testosterone action, lowering the tendency of testosterone drugs to produce androgenic side effects. It is important to remember that both anabolic and androgenic effects are mediated via the cytosolic androgen receptor. Complete separation of testosterone’s anabolic and androgenic properties is not possible, even with total 5-alpha reductase inhibition.