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Unlike methyltestosterone, owing to the presence of its C1(2) double bond, metandienone does not produce 5α-reduced metabolites. The drug [is dianabol legal](https://quickfixinterim.fr/employer/buy-dianabol-10mg-online-we-deliver-worldwide/) metabolized in the liver by 6β-hydroxylation, 3α- and 3β-oxidation, 5β-reduction, 17-epimerization, and conjugation among other reactions. It has very low affinity for [https://robbarnettmedia.com/employer/understanding-dianabol-comprehensive-guide-to-pills-and-tablets-for-enhanced-muscle-growth](https://robbarnettmedia.com/employer/understanding-dianabol-comprehensive-guide-to-pills-and-tablets-for-enhanced-muscle-growth/) human serum sex hormone-binding globulin (SHBG), about 10% of that of testosterone and 2% of that of DHT. As with other 17α-alkylated AAS, [ipo.fountain.agri.ruh.ac.lk](https://ipo.fountain.agri.ruh.ac.lk/employer/anabolic-steroid-misuse/) metandienone may be hepatotoxic, especially with prolonged use of high doses. 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