Methyldrostanolone 10 mg

• Brand: Swiss Remedies
• Category: Oral AAS Research Compound
• Content: 100 tablets | 10 mg per tablet (1,000 mg total)
• Manufactured in: Switzerland

Product Overview

Methyldrostanolone 10 mg — commonly referenced as “Superdrol” in unregulated contexts — is a

synthetic anabolic–androgenic steroid (AAS) structurally derived from the dihydrotestosterone (DHT) family.

Its 17--alkylated modification grants oral bioavailability, making it a preferred laboratory reference compound

for studies involving androgen receptor (AR) activation, metabolic processing, toxicity profiling, and comparative

AAS analysis.

Methyldrostanolone is valued in research due to its strong anabolic properties, high potency, and well-defined

chemical identity. These attributes make it a useful benchmark in experiments requiring a consistent anabolic

signal or a known control compound for evaluating novel steroids and metabolites.

Key Research Highlights

Strong anabolic transcriptional activity:

Acts as an AR agonist, stimulating protein synthesis, nitrogen retention, and anabolic gene expression.

Metabolic and toxicology profiling:

Its oral, methylated structure elevates hepatic workload, making it suitable for liver-stress and enzyme-induction models.

Comparative AAS evaluation:

Serves as a reference steroid in potency and toxicity benchmarking across DHT-derived and testosterone-derived analogs.

AR signaling studies:

Frequently used in cell-based and animal models for androgen receptor pathway research.

Suggested Laboratory Applications

• Androgen receptor (AR) activation modeling
• Protein synthesis and anabolic gene-expression studies
• Comparative steroid potency and toxicology profiling
• Liver-injury and hepatotoxicity research on oral 17--alkylated compounds
• Metabolic analysis and steroid biotransformation pathways

Technical Specifications

PubChem-Supported Research Insights

• Binds the androgen receptor with strong anabolic transcriptional response
• Promotes increased protein synthesis and nitrogen retention
• 17--alkylation contributes to oral bioavailability and elevated hepatotoxic stress
• Useful for comparing metabolic pathways of DHT-based steroids
• Helpful in toxicology assays assessing oxidative and lipid metabolism alterations

Documented Research Side Effects

• Hepatic stress: enzyme elevation, cholestatic patterns, potential hepatotoxicity
• Disrupted lipid metabolism (low HDL, elevated LDL)
• Possible cardiovascular strain under prolonged exposures
• Endocrine suppression of natural steroid biosynthesis
• Hormonal dysregulation in chronic models

Handling & Compliance

For Research Use Only — not for human or veterinary consumption.

Store in a dry, temperature-stable environment; protect from light.

Controlled or restricted status in many jurisdictions; ensure compliance before acquisition or use.

Suitable only for qualified laboratories conducting analytical, forensic, or experimental research.