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Lexicon

YK11

A special case: structurally a steroid derivative that acts like a SARM and is additionally described as a myostatin inhibitor, with very thin data.

2 min read 12 sources

White tablet bottle with a dark TPD label on a white podium, next to it a large blue 3D molecule model with white atoms in a bright lab, symbolic image for YK11
Preclinical · not approved

Summary

At a glance

Sources checked on 26 Oct 2026

Human trials in the registry
0 trials

no trial with YK11 on ClinicalTrials.gov, as of 26 Oct 202611

Molecular weight
430.5 g/mol

steroid backbone, unlike most SARMs12

Found in urine
14 metabolites

intact YK11 did not appear in urine, some products detectable for more than 48 hours9

Rat study on the brain
5 weeks

more oxidative stress and inflammation in the hippocampus, poorer memory8

  • YK11 has a steroid backbone but behaves like a selective androgen receptor modulator in cell studies: it activates the receptor only partially and only at certain genes.212
  • In mouse muscle cells YK11 stimulated the production of follistatin, an opponent of myostatin. An antibody against follistatin cancelled the effect.1
  • In bone cells YK11 promoted growth and mineralisation, in rats bone defects healed better with a YK11 gel.45
  • In rats given YK11 for five weeks oxidative stress and inflammation in the hippocampus rose and memory got worse.78
  • ClinicalTrials.gov lists no human trial (as of October 2026), but YK11 has already been found in doping samples. Everything here is preclinical research, not a recommendation.1110
Profile

Updated May 2026

Class
SARM-like steroid derivative
Use
Oral

often split

Status
Preclinical only

no human data

WADA
Banned
Sizes
10 mg

1 size in the shop

Contents 14 sections
  1. At a glance
  2. What is YK11?
  3. How it works
  4. How to take it
  5. Dosing
  6. What the research shows
  7. Research status
  8. Side effects
  9. Practice
  10. Storage
  11. Related compounds
  12. FAQ
  13. Glossary
  14. Sources

What is YK11?

YK11 is a special case among the SARM-like compounds. Structurally it is a steroid derivative but it behaves like a selective androgen receptor modulator. It has additionally been described in cell models as a myostatin inhibitor, a compound that could loosen the muscle's natural growth brake.

Up front: there are essentially no human data on YK11. Everything available comes from cell culture.

Comparison

YK11 and other SARMs

All bind the androgen receptor, as described in the TPD lexicon. Tap a card to open its entry.

Simplified: YK11 is the only compound here with a steroid backbone. The route via follistatin is known only from cell culture, there is no comparison in humans. 21

How it works

YK11 activates the androgen receptor as a partial agonist. In muscle cells it increased the production of follistatin, an endogenous counterpart to myostatin. Since myostatin brakes muscle growth, more follistatin would theoretically be a lever for more growth.

Important: this is described in C2C12 muscle cells, not in humans. Whether and how strongly it transfers is open.

Where it acts

Where YK11 acted in cell and animal studies

Tap a point or a card. Colour = androgen receptor, grey = observed. No data from humans.

  1. Muscle cells

    More follistatin and muscle control factors than with DHT, cells matured faster (cell culture)1

    AR
  2. Bone

    Bone cells grew and mineralised more, defects in rats healed better5

    AR
  3. Brain (hippocampus)

    In rats more inflammatory messengers and oxidative stress, poorer memory8

    Observed in trials
  4. Blood (inflammation)

    In mice with sepsis fewer inflammatory messengers and fewer deaths6

    Observed in trials

Known targets2

Compound PubChem CID 119058028 (YK11): one described target, Partial agonist in cell studies, without N/C interaction.

Androgen receptor
Gene
AR
UniProt
P10275
ChEMBL
CHEMBL1871
Action
Partial agonist in cell studies, without N/C interaction
Close-up of translucent light blue muscle fibres with blue and white molecule chains and dark spheres between them
In cell studies via the androgen receptor and follistatin. Symbolic image.

How to take it

Oral, often split across two doses.

  • Because of the shorter duration of action, it is frequently split.
  • With some water, with or without food.
  • Cycles are kept short.
White tablet bottle with a dark TPD label, three white tablets in front, a glass of water beside it on a bright table
Tablets taken by mouth. Symbolic image.

Dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts

What the research shows

The central study (Kanno, 2013) showed that YK11 in C2C12 muscle cells stimulated the production of follistatin and through it promoted myogenic differentiation. The effect could be reversed with a follistatin antibody, which supports the mechanism.

This is a clean preclinical work but it is cell culture. There are no human studies, no human pharmacokinetics and no long-term data. YK11 is clearly experimental.

Top view of petri dishes and pipettes around a glass bundle of red muscle fibres and an open glass padlock
So far only cell culture and animal studies. Symbolic image.

Research status

Where the research stands

YK11 has never been tested in a registered human trial. The data come from cell cultures and studies in mice and rats. As of 26 Oct 2026. 11

  1. Preclinical Cell studies since 2011, later mice and rats
  2. Phase 1 no registered trial
  3. Phase 2 no registered trial
  4. Phase 3 no registered trial
  5. Approval not yet
Not approved and no registered human trial. Doping laboratories know YK11 and have detected it in a competition sample.11

So far there is no registered trial in humans. 11

Side effects

  • The case literature on SARM-like compounds documents liver strain. For YK11 the window is judged especially narrow.
  • As an androgenically active compound, suppression of the body's own axis is to be expected.
  • Solid human side-effect data simply do not exist.

Practice

  1. Keep expectations on the floor, everything rests on cell models.

  2. If at all, very low and short.

  3. Banned in official competition.

  4. Keep an eye on liver and blood values.

Two light blue dumbbells, a shaker with a pale drink and a folded light blue towel on a wooden floor

Storage

Store dry, cool and protected from light, out of reach of children. Keep the original container closed and mind the expiry date.

Three white tablet bottles and a folded light blue towel on a white shelf
Dry, cool and protected from light in the closed original container. Symbolic image.

Related

Related compounds

Same targets: all in the TPD lexicon.

FAQ

Common questions about YK11

Short answers, each backed by the sources below.

Has YK11 been studied in humans?

No. As of 26 October 2026 ClinicalTrials.gov lists no trial with YK11. All data come from cell cultures and studies in mice and rats. There is no study on absorption, half-life or tolerability in humans.111

Why is YK11 called a SARM although it is a steroid?

Its discoverers found in 2011 that YK11 activates the androgen receptor only partially. It moves the receptor into the nucleus but does not trigger the folding that DHT triggers. Depending on the gene it acted more strongly or more weakly than a full androgen. They call this pattern selective modulation.23

What does YK11 have to do with myostatin?

In C2C12 mouse muscle cells YK11 stimulated the production of follistatin, DHT did not. Follistatin slows myostatin, the body's own growth brake for muscle. An antibody against follistatin cancelled the faster maturation of the cells. Whether the same happens in a living body has not been studied.1

What do the animal studies show?

In rats skull bone defects healed better with a YK11 gel. Blocking the androgen receptor slowed this. In mice with sepsis inflammatory messengers and deaths fell. A Brazilian group gave rats YK11 for five weeks: in the hippocampus oxidative stress and inflammation rose, the mitochondria worked worse and memory suffered.5678

Is YK11 found in doping tests?

Yes. The Cologne doping laboratory described fourteen metabolites in urine in 2018, intact YK11 was not among them. Conjugated metabolites were detectable for more than 48 hours. A laboratory in Los Angeles reported a positive doping sample in 2023.910

Which risks are known?

Solid data from humans are missing. The rat studies show damage in the hippocampus. The authors explicitly warn against use by athletes. As a compound that activates the androgen receptor, an effect on the body's own hormone axis is plausible, but it has not been measured.782

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

Androgen receptor
Docking site for testosterone and DHT inside the cell. When activated it switches on genes for muscle, bone and sex characteristics.
C2C12 cells
Muscle precursor cells from mice, a standard lab model.
DHT
Dihydrotestosterone, a strong androgen made by the body and the comparator in the cell studies.
Follistatin
A protein made by the body that captures myostatin and so loosens the brake.
Hippocampus
Brain region that is important for learning and memory.
Metabolite
A substance into which the body converts a compound. Doping labs often look for these rather than the compound.
Myostatin
A protein made by the body that slows muscle growth.
Oxidative stress
An excess of reactive oxygen particles that can damage cells.
Partial agonist
A compound that activates a receptor, but not as strongly as the body's own messenger.
Preclinical
Research before first use in humans, in cell cultures and animal models.
SARM
Selective androgen receptor modulator: a compound that activates the androgen receptor to different degrees depending on tissue or gene.

Evidence

Sources

Show all 12 sourcesHide sources 10 Studies1 Trial registry1 Database checked 26 Oct 2026

Studies

  1. YK11 controls muscle cell maturation via follistatin (cell culture)

    Kanno et al., Biological and Pharmaceutical Bulletin, 2013

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  2. YK11 as a partial agonist of the androgen receptor (cell culture)

    Kanno et al., Biological and Pharmaceutical Bulletin, 2011

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  3. Why YK11 switches different genes than DHT (cell culture)

    Kanno et al., Experimental Cell Research, 2022

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  4. YK11 promotes bone cells via the androgen receptor (cell culture)

    Yatsu et al., Biological and Pharmaceutical Bulletin, 2018

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  5. YK11 and the healing of bone defects (cells and rats)

    Wang et al., Journal of Molecular Endocrinology, 2025

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  6. YK11 in sepsis (mice)

    Lee et al., Biochemical and Biophysical Research Communications, 2021

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  7. Oxidative stress and mitochondria in the hippocampus (rats)

    Dahleh et al., Journal of Steroid Biochemistry and Molecular Biology, 2023

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  8. Inflammation and memory in the hippocampus (rats)

    Dahleh et al., Chemico-Biological Interactions, 2024

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  9. YK11 metabolites for doping control

    Piper et al., Drug Testing and Analysis, 2018

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  10. Detection of YK11 in a doping sample

    Sobolevsky et al., Drug Testing and Analysis, 2024

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Search on ClinicalTrials.gov (no trial with YK11)

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. Structure of YK11 in PubChem

    PubChem, U.S. National Library of Medicine (CID 119058028)

    Checked 26 Oct 2026 via PubChem

In the shop

YK11 in the catalog

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