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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). Because of its fairly weaker strength than Dianabol, the doses required to elicit effects from Tbol are considered to be quite high (this will be explained shortly in the Tbol doses section of this profile). In general, athletes and bodybuilders can expect steady and quality lean mass gains with no risk of any bloating, gyno, or any other estrogenic effects. Mass and strength gains are not known to be dramatic due to its lack of anabolic strength, but steady and quality lean gains that grow consistently over time can be expected. It is also used as an ideal cutting agent during periods of fat loss or pre-contest preparation due to its inability to convert into Estrogen. Turinabol’s capabilities really shine as an adjunct to other anabolic steroids when it is run (stacked) with other anabolic steroids due to its ability to bind to SHBG. 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. There is no such thing as a ‘perfect steroid’, and although Turinabol comes close, it is still not without its potential risks and side effects. However, Turinabol can easily be considered a member of the trio of ‘almost perfect’ anabolic steroids: Anavar, Primobolan, and Turinabol. Turinabol is a modified form of Dianabol, and while Dianabol does hold a moderate affinity for aromatization into Estrogen, Turinabol does not at all. This is the result of its 4-chloro substitution (the chloro group that has been affixed to the 4th carbon on the steroid structure), which disallows the opportunity for the aromatase enzyme to convert Turinabol into Estrogen. Turinabol is therefore not aromatized at any dose at all, and estrogenic side effects should not be considered a part of Turinabol side effects at all. Turinabol’s chemical modification of holding a double-bond between carbons 1 and 2, as well as the 4-chloro modification, grant it with a significantly reduced androgenic strength, gp helios 40 mcg / 6mg injectable steroids $18.00 elios. However, this has not eliminated Turinabol’s androgenic capabilities and although it is vastly less androgenic than most other anabolic steroids, there is still a risk with androgenic side effects (especially in those very sensitive to androgenic side effects). At lower to mid-range doses, androgenic effects should rarely be experienced due to its weakness in this department, but higher doses will elicit a greater androgenic effect, especially in females. In addition, Turinabol is indeed metabolized by the 5-alpha reductase enzyme into a stronger androgenic metabolite, but the rate of 5AR reduction that Turinabol is exposed to is known to be very minimal, and so the use of 5AR inhibitors such as Proscar, FInasteride, Dutasteride, etc. The potential for androgenic Turinabol side effects include: increased sebum secretion (oily skin), increased bouts of acne (linked to increased sebum secretion), bodily and facial hair growth, benign prostatic hypertrophy (BPH), and the increased risk of triggering Male Pattern Baldness (MPB) in individuals that possess the genetic trait required for the condition to manifest itself. Women will increase their chances of experiencing virilization at doses greater than 10mg per day. HPTA AND ENDOGENOUS TESTOSTERONE PRODUCTION SIDE EFFECTS.
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