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oralanabolic

Methylstenbolone

UltradrolM-Sten2,17α-dimethyl-5α-androst-1-en-17β-ol
660
Anabolic Ratio
190
Androgenic Ratio
0.25d
Half-Life

Designer prohormone/AAS briefly sold legally in the US (2010–2012) before DEA scheduling. 2-methyl, 17α-methyl DHT derivative. Produces rapid strength and size gains. Very hepatotoxic with notable cardiovascular impact. Limited human pharmacokinetic data available.

Mechanism of Action

DHT-derived — no aromatization. 2-methyl modification increases anabolic potency similarly to methasterone. 17α-methylation provides oral activity. High AR binding affinity documented in vitro. No 5α-reduction pathway. SHBG binding may contribute to libido-altering effects.

Methylstenbolone molecule
Molecular structure

Typical Dosing

56 mg
low / week
112 mg
moderate / week
196 mg
high / week

⚠ Warning Flags

  • Very limited human safety data
  • Hepatotoxic — liver enzymes elevate rapidly
  • DEA Schedule III in the US

Effect Profile

Muscle Protein Synthesis
6Moderate
Nitrogen Retention
6Moderate
Strength Gains
7High
Red Blood Cell Production
2Minimal
Fat Loss
4Low
Glycogen Storage
5Moderate
Recovery Speed
5Moderate
Collagen Synthesis
2Minimal

Side Effect Profile

Hormonal Suppression
7High
Estrogenic Effects
1Minimal
Androgenic Effects
5Moderate
Cardiovascular Strain
6Moderate
Liver Stress
7High
Insulin Resistance
4Low
Mood Changes
5Moderate
Prostate Risk
3Low

Research Studies

Identification and detection of designer steroids in supplements: methylstenbolone

Geyer H, et al. · 2011

PubMed

Methylstenbolone was identified in commercially sold prohormone products; doping control urine analyses confirmed its metabolites and established detection windows of 3–5 days post-cessation.