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Healing & Recovery
Preclinical

YK-11

YK-11

Also known as: YK11, YK-11 Myostatin Inhibitor

Overview

Key Facts

Primary Goal: Research and therapeutic applications of YK-11

Partial agonist at the androgen receptor, inducing selective gene transcription in muscle tissue. Increases expression of follistatin in C2C12 myoblasts, indirectly inhibiting myostatin.

Dosing Information

Half-Life

6-10 hours (estimated, limited pharmacokinetic data)

Typical Dose

5–15 mg

Frequency

Once daily (oral or injectable, split AM/PM by some researchers)

Cycle Length

6-8 weeks (with post-cycle therapy consideration)

Administration Routes:
intramuscularoral

Benefits

  • Dual mechanism: androgen receptor activation plus myostatin inhibition via follistatin
  • May promote muscle growth exceeding traditional SARMs
  • Selective anabolic effects with potentially reduced androgenic side effects
  • Increases follistatin expression in myocytes
  • Oral bioavailability eliminates need for injections in some formulations

Side Effects

Potential liver toxicity (methylated steroidal structure)mild
Testosterone suppression requiring post-cycle therapymild
Hair loss in predisposed individuals (DHT-derived)mild
Joint dryness (anti-estrogenic environment)mild
Aggression and mood changesmild
Extremely limited human safety datamild

Mechanism of Action

1

Partial agonist at the androgen receptor, inducing selective gene transcription in muscle tissue

2

Increases expression of follistatin in C2C12 myoblasts, indirectly inhibiting myostatin

3

Steroidal backbone (19-nor DHT derivative) provides androgen receptor binding affinity

4

Does not appear to induce full AR conformational change, leading to gene-selective effects

5

Downstream Akt phosphorylation promotes anabolic signaling in skeletal muscle

Contraindications

Do not use this peptide if any of the following apply:

  • Pre-existing liver disease or elevated liver enzymes
  • Women of childbearing potential (steroidal compound)
  • Adolescents or those with open growth plates
  • History of hormone-sensitive cancers
  • Concurrent use of hepatotoxic medications

Storage & Reconstitution

Unreconstituted (Powder)

Temperature15–25°C (59–77°F)
DurationUp to 3 months

Reconstituted (Mixed)

Temperature15–25°C (59–77°F)
Duration2-4 weeks

Research Summary

Preclinical

YK-11 was first described by Kanno et al. (2011) in a study on C2C12 myoblast cells, demonstrating that it induced myogenic differentiation and increased follistatin expression more effectively than DHT. Subsequent in vitro studies confirmed its dual AR-agonist and myostatin-inhibiting activity. No in vivo animal or human clinical trials have been published. Its classification remains debated — it shares features with both SARMs and anabolic steroids. Extreme caution is warranted due to the complete absence of clinical safety data.

Frequently Asked Questions

Common questions about YK-11

UK-Specific Information

Exclusive data points and guidance for UK residents using YK-11

UK Lab Testing

UK Lab Testing

Recommended labs: Medichecks, Thriva (£89-£149 for peptide safety panel)

Why this matters: UK-specific lab testing guidance not available on US competitor sites

Commonly Stacked With

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