[h=2]M-Drol/S-drol/Superdrol[/h]
Nomenclature: 17β-Hydroxy-2α,17α-dimethyl-5α-androstane-3-one or 2a,17a-dimethyl-etiocholan-3-one, 17b-ol or (more accurately) 2a,17a-dimethyl-etioallocholan-3-one, 17b-ol
Synonyms: Superdrol, Methasterone, Methyl Masteron, M-Drol, S-Drol
Originally brought to market by Designer Supplements (then licensed to Anabolic Xtreme), this designer steroid is a 17a-methylated version of the injectable steroid masteron. Since we know 17a-methylation doesn't just increase oral bioavailability, it also changes the effect of the steroid, it may be more useful to consider superdrol as 17a-methyl-DHT with an additional 2-methyl (methyl groups at C1,C2, 17a, and 7a all increase anabolic activity). In fact, superdrol is one of the most potent anabolic steroids ever brought to market. Sadly, it's also one of the most toxic, as evidenced by a number of medical case studies of people hospitalised with cholestatic jaundice and worse. It's for this reason that cycles must be kept short and relatively low dosed. Due to it's structure, it can't aromatise, which means any gyno sides are typically post-cycle. On-cycle lethargy is common, as are shin and back pumps.
Please ignore people who suggest that CEL M-drol is an inferior "b-isomer" version of superdrol, citing the nomenclature as evidence. The fact that they label it etiocholan instead of etioallocholan is a labelling error, not an indication that it contains the wrong compound. People who claim that it's the 5b-reduced isomer fail to understand the dramatic difference that makes to the shape of the steroid (it bends the A-ring away from the plane of the steroid) which dramatically reduces receptor binding affinity (5a-DHT has 173 times stronger binding affinity than 5b-DHT for example). The flatter the better, as far as androgen receptors are concerned. To put it bluntly, if it were the 5b version it would not work (which it does, so it isn't).
Cycles are typically 10 - 30mg for three to four weeks, followed by a SERM PCT protocol.
Nomenclature: 17β-Hydroxy-2α,17α-dimethyl-5α-androstane-3-one or 2a,17a-dimethyl-etiocholan-3-one, 17b-ol or (more accurately) 2a,17a-dimethyl-etioallocholan-3-one, 17b-ol
Synonyms: Superdrol, Methasterone, Methyl Masteron, M-Drol, S-Drol
Originally brought to market by Designer Supplements (then licensed to Anabolic Xtreme), this designer steroid is a 17a-methylated version of the injectable steroid masteron. Since we know 17a-methylation doesn't just increase oral bioavailability, it also changes the effect of the steroid, it may be more useful to consider superdrol as 17a-methyl-DHT with an additional 2-methyl (methyl groups at C1,C2, 17a, and 7a all increase anabolic activity). In fact, superdrol is one of the most potent anabolic steroids ever brought to market. Sadly, it's also one of the most toxic, as evidenced by a number of medical case studies of people hospitalised with cholestatic jaundice and worse. It's for this reason that cycles must be kept short and relatively low dosed. Due to it's structure, it can't aromatise, which means any gyno sides are typically post-cycle. On-cycle lethargy is common, as are shin and back pumps.
Please ignore people who suggest that CEL M-drol is an inferior "b-isomer" version of superdrol, citing the nomenclature as evidence. The fact that they label it etiocholan instead of etioallocholan is a labelling error, not an indication that it contains the wrong compound. People who claim that it's the 5b-reduced isomer fail to understand the dramatic difference that makes to the shape of the steroid (it bends the A-ring away from the plane of the steroid) which dramatically reduces receptor binding affinity (5a-DHT has 173 times stronger binding affinity than 5b-DHT for example). The flatter the better, as far as androgen receptors are concerned. To put it bluntly, if it were the 5b version it would not work (which it does, so it isn't).
Cycles are typically 10 - 30mg for three to four weeks, followed by a SERM PCT protocol.
