Mibolerone

Cheque Drops · Upjohn U-15614

Anabolic Steroid aas Oral Case Studies / Guidelines

Half-life

4 hr

Time to Peak

1 hr

Steady State

~1 days

Dose Range

1–10 mcg

Frequency

As needed

Overview

Extremely potent oral androgen (veterinary compound — originally used to suppress estrus in dogs). Used by some bodybuilders pre-competition or pre-contest for acute aggression and CNS stimulation. Among the most androgenic compounds ever used by athletes (estimated ~1800–2500% androgenic relative to methyltestosterone). Harm reduction: Doses above 5mcg dramatically increase hepatotoxicity and cardiovascular risk. Duration strictly limited to 2–4 weeks maximum. Significant progestogenic activity — monitor prolactin. Very short half-life (~4 hours) — used only on training/competition days. Extremely hepatotoxic — TUDCA mandatory.

Mechanism of Action

Progestin-derived androgen. Binds androgen receptor with very high affinity. Also binds progesterone receptor — progestogenic side effects expected. No aromatisation to estrogen. 17-alpha-alkylated — significant hepatotoxicity.

Dosing Information

Route Dose Range Half-life Tmax Frequency
Oral 1–10 mcg 4 hr 1 hr As needed

Storage & Handling

Room temperature — Store at 20-25C. Protect from light. Liquid solution.

Used in Regimens

Mibolerone is not currently part of any catalog regimen.

Data Sources

  • Community r/steroids Compound Experience Directory

Related Tools

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Doseline provides informational tools only. It is not a medical device and does not provide medical advice. Always consult a qualified healthcare provider.