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Introducing Ergopharm 1-AD Phoromone Nutritional Supplement : It’s time to introduce what Patrick refers to as “the crown achievement” of his career. The formal chemical name of the compound Patrick developed is 1-androstene-3beta, 17beta-diol. They nicknamed this compound “1-AD” which is a shortened acronym of its chemical name.
You probably are familiar with the “Andro” prohormones, and the “Norandro” prohormones. The former convert to testosterone and the latter to 19-nortestosterone. Ergopharm 1-AD Phoromone Nutritional Supplement, however, does not fit into either of those categories. That is because Ergopharm 1-AD Phoromone Nutritional Supplement converts to a relatively unheard of hormone called 1-testosterone. 1-testosterone is what is known as a “double bond isomer” of testosterone.
Although chemically the only difference between testosterone and 1-testosterone is the position of the double bond, pharmacologically the two products are quite different. According to research done by the pharmaceutical giant G.D. Searle and published in the 1960s, 1-testosterone is over 7 times as myotrophic (anabolic) as testosterone. That makes 1-testosterone a phenomenally potent compound, surpassing even most synthetic anabolic steroids.
No Aromatization : 1-testosterone differs from testosterone in another way as well. Being a 5alpha-reduced androgen (a DHT derivative) it simply cannot aromatize to estrogens. The same goes for Ergopharm 1-AD Phoromone Nutritional Supplement itself - no estrogen transformation can occur. This makes Ergopharm 1-AD Phoromone Nutritional Supplement unique compared to other prohormones — all of which can either aromatize directly, convert to a product that aromatizes, or both. So what does this mean in the real world? It means that your chances of getting gynecomastia (bitch tits) from Ergopharm 1-AD Phoromone Nutritional Supplement is essentially zero, and that water retention side effects are vastly reduced compared to other prohormones.
The Only Truly “Orally Active” Prohormone : Natural androgenic steroids are normally not very active orally. Large amounts have to be taken orally to see biological effects. This is because the first pass through the liver causes a massive deactivation of the compounds, primarily through the oxidation of the 17beta-hydroxyl to a 17-keto group. Chemists long ago found that by adding an alkyl (methyl or ethyl) chemical group to the alpha position of the 17 carbon, this oxidation can be prevented. However, this alkyl derivatization also greatly increases the liver toxicity. Therefore the usage of such synthetically altered compounds (methyltestosterone, oxymetholone, stanozolol) are not without substantial risk.
Luckily, there are other ways to render a steroid orally active, and do so without making the compound toxic to the liver. Certain structural modifications can alter the metabolism of steroids making them resistant to liver breakdown. One of these modifications is unsaturation (presence of a double bond) in the 1-position. One steroid that has this structural modification and is orally active is the anabolic steroid Methenolone, also known as Primobolan.
This double bond position that makes Primobolan orally active is the same one found in Ergopharm 1-AD Phoromone Nutritional Supplement, which, by the way, is also orally active. Steroids with this particular double bond characteristic are known as 1-dehydroandrostanes.
During the 60’s and 70’s some papers Theyre published describing the phenomenon of oral activity seen with 1-dehydroandrostanes, including 1-testosterone and Ergopharm 1-AD Phoromone Nutritional Supplement. What was discovered was that these compounds resist metabolic deactivation by profoundly shifting what is known as the “17-keto redox potential” towards the formation of active 17beta-hydroxyl steroids(2,3). What does this mean? It means that when you take Ergopharm 1-AD Phoromone Nutritional Supplement, the liver serves primarily to activate the compound, rather than break it down and excrete it as it does with other prohormones and testosterone. It means that 1-AD is “orally active,” yet it does not impart the liver toxicity that 17alpha-alkylation does.
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