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Turinabol is C17-alpha alkylated so as to allow oral bioavailability, and as a result, will exhibit a measure of liver toxicity. It also possesses a double bond between carbon 1 and carbon 2 (also known as the 1-ene carbon), and it is this double-bond that is responsible for the reduction of androgenic strength. Lastly, as previously mentioned, a chloro group has been added at the 4th carbon, responsible for rendering it unable to aromatize as well as reducing the androgenic strength even further. Because of its distinct separation of its androgenic to anabolic effects, it is a weaker anabolic steroid than its parent hormone Dianabol. However, the assurance with Tbol is that with any apparent muscle building capability, it will present much less in the way of androgenic effects and absolutely no estrogenic effects (due to its inability to aromatize into Estrogen). 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Binding to SHBG allows more of the other anabolic steroids it is stacked with to be available to do their job, being uninhibited by SHBG, which is another advantage that it exhibits. Turinabol is one of the anabolic steroids that is regarded as a very ‘mild’ anabolic steroid in regards to side effects. Other similar anabolic steroids in this category include Anavar (Oxandrolone) and Primobolan (Methenolone), both regarded as almost perfect anabolic steroids due to their strong dissociation between anabolic and androgenic effects, as well as the fact that they cannot convert into Estrogen at any dose at all. Turinabol indeed shares all of these characteristics, and in fact possesses an androgenic strength rating that is the lowest out of all three compounds with a measurement of 6 versus 24 for Anavar and 44 ‘ 57 for Primobolan. It can therefore be said that Turinabol side effects are almost nonexistent, but there are still some considerations and risks to be known and understood. 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