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Methenolone is an anabolic androgenic steroid that was first released in 1962 by squibb under the trade name nibal (oral) and nibal depot (injectable)in the United States. It is an inhibitor of steroidogenic proteins and is thought to increase its potency if applied as a topical agent and/or given as an orally administered drug, particularly in the presence of a high concentration of testosterone. In addition, it has also been shown to have potent antitumor activity, primobolan oral.[ 2 ] It is present in various cosmetic compositions.[ 3 ] 1.2. Physical Characteristics Synonyms: 4-hydroxy-1,1-pentanediplone (4-OH-diphenbutane) (incl, buy genotropin online reviews.), buy genotropin online reviews. 1, methenolone acetate half-life.3, methenolone acetate half-life. Human Pharmacology 1, buy genotropin online reviews.3, buy genotropin online reviews.1, buy genotropin online reviews. Pharmacokinetics 3,4-dihydroxy-1,1-pentanediplone is converted mainly by CYP-mediated metabolism into dihydrotestosterone in liver, methenolone acetate injectable. Dihydrotestosterone is a testosterone metabolite known to be a substrate for the human CYP-1B enzyme. The amount generated varies depending on the mode of administration (i, buy genotropin.e, buy genotropin. oral, injectable, or topical), a patient's age, and type of test, buy genotropin.[4] Testicular testosterone (DHT) is also produced by this enzyme, although the amount of DHT produced varies depending on the patient's age and the type of test, buy genotropin turkey.[4] The conversion of the dihydrotestosterone to DHT is a process with a mean C max of 1.1µg/ml and a half-life of 15 hours.[5] 4-hydroxy-1,1-pentanediplone is a potent androgenic anabolic steroid, with an initial half-life of 1, buy genotropin turkey.1µg/ml and an elimination half-life of 15 hours, buy genotropin turkey.[5] It has not been shown as a potent androgen receptor modulator[6] and there is no evidence that it is any more potent or penetrable than other anabolic steroids. Because of its ability to induce androgenic changes with high potency and anabolic potential, 4-hydroxy-1,1-pentanediplone and 4-hydroxy-3,3-dihydroxytestosterone are generally considered to be potent anabolic steroids, methenolone acetate half-life. However, they are often considered to be less potent and less potent androgenic than synthetic androgenic anabolic steroids, such as conjugated equine estrogen (CEEE).


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