YK-11 is a lab-made steroid that researchers at Toho University in Japan described in 2011 as a partial activator of the androgen receptor (Kanno 2011). It is sold as a SARM and a “myostatin inhibitor”, but both ideas come from cell and rodent studies: it has never been tested in a human trial, and ClinicalTrials.gov lists none (ClinicalTrials.gov). The human harms on record come from case reports and an FDA warning about a product linked to a stroke (FDA). It is not approved anywhere, and WADA bans it (WADA 2026).

Below: what YK-11 is, every study we found, what it does and does not do, its side effects, how it compares with RAD-140, LGD-4033 and steroids, its legal status, and links to all of our YK-11 guides. This page also replaces our older complete guide to YK-11.

What is YK-11?

YK-11 (also written YK11, and sold as Myostine) has a steroid skeleton: it is a 19-norpregnane derivative, unlike nonsteroidal SARMs such as ostarine or RAD-140 (Kanno 2011; PubChem CID 119058028; UK Anti-Doping). Its discoverers found that it switches on the androgen receptor only partly, without the receptor’s usual N/C-terminal interaction, and that its effect differs from gene to gene, which is why they called it a selective androgen receptor modulator (Kanno 2011). Anti-doping scientists describe it as “the steroidal SARM YK-11” (Thevis 2017), and WADA lists it with the SARMs (WADA 2026).

Chemical structure of YK-11, a steroidal androgen receptor partial agonist
YK-11 is built on a steroid skeleton, which sets it apart from nonsteroidal SARMs.

We found no record of a company developing YK-11 as a medicine. All published research is in cells, rats and mice, plus anti-doping lab work (ClinicalTrials.gov).

YK-11 research at a glance

Study Model What it found Evidence
Kanno 2011 Human breast cancer cells (MDA-MB 453) Partial activation of the androgen receptor; gene-selective effects. Cell
Kanno 2013 Mouse muscle cells (C2C12) Raised muscle-building signals (MyoD, Myf5, myogenin) more than DHT and raised follistatin; an anti-follistatin antibody reversed the effect. Cell
Yatsu 2018 Mouse bone-forming cells More cell growth and mineralization; an androgen receptor blocker weakened the effect. Cell
Wang 2025 Rats with skull bone defects A YK-11 hydrogel placed in the defect helped the bone repair. Animal
Lee 2021 Mice with sepsis Lower inflammatory signals and organ-damage markers; fewer deaths. Animal
Dahleh 2023, 2024 (Dahleh 2023; Dahleh 2024) Rats, 5 weeks Oxidative stress, inflammation and mitochondrial damage in the hippocampus; impaired memory consolidation. Swimming exercise blunted some changes. Animal
Piper 2018 Anti-doping elimination study No intact YK-11 in urine; 14 breakdown products, some traceable for more than 48 hours. Anti-doping study

No study has tested YK-11 for muscle, strength, fat loss or safety in people (ClinicalTrials.gov). Compare its evidence with other compounds in the SARMs database.

What does YK-11 do? Benefits vs evidence

Muscle growth and the “myostatin inhibitor” claim

The claim rests on one cell study. In mouse muscle cells, YK-11 raised follistatin, a protein that blocks myostatin, and that drove muscle-cell differentiation; blocking follistatin reversed the effect (Kanno 2013). No human study has measured myostatin, follistatin or muscle with YK-11. The one animal study that used it as a myostatin inhibitor was in mice with sepsis: it reported less inflammation, less organ damage and fewer deaths, not muscle growth in healthy animals (Lee 2021). “Myostatin inhibitor” describes a lab-dish mechanism, not a measured effect on muscle in people.

Strength and fat loss

Not studied. We found no trial, animal study or cell study of strength or fat loss with YK-11.

Bone

In cells, YK-11 increased bone-forming activity (Yatsu 2018), and in rats a YK-11 gel placed directly into a skull defect sped up repair (Wang 2025). That is local application in an animal, not evidence about swallowing it.

Is YK-11 the strongest SARM?

There is no way to rank it, because it has never been tested in people and no study has compared its effect on muscle with other SARMs. No published study has measured an anabolic-to-androgenic ratio for YK-11 either. “Strongest” claims come from user reports, which cannot separate YK-11 from training, diet, other compounds or a mislabeled product.

YK-11 results and before-and-after reports

There are no measured results. User reports and photos are collected on YK-11 before and after, with the evidence alongside, and the 8-week YK-11 log is one user’s account.

YK-11 side effects

Side effect What was found Evidence
Stroke after a product sold as YK-11 FDA tested a bodybuilding product after a consumer who used it had a stroke. It contained YK-11, as labeled, plus an undeclared anabolic steroid (trendione) (FDA). Regulator warning
Cholestatic liver injury (with other SARMs) A young active-duty US Marine developed jaundice (bilirubin 29.2 mg/dL) after about 3 months of LGD-4033, RAD-140 and YK-11 and needed hospital care (Lee 2023; Leciejewska 2024). Case report
FDA adverse event reports Two reports name YK-11: liver failure in a 23-year-old man (2019) and stroke with tingling in a 37-year-old man (2020). Matching reports also name LGD-4033 and RAD-140, so several SARMs were probably involved (Leciejewska 2024). Adverse event reports
Brain changes Oxidative stress, inflammation and impaired memory consolidation in rats after 5 weeks (Dahleh 2023; Dahleh 2024). Animal
Wrong or mislabeled product Of 44 products sold online as SARMs, 25% contained substances not on the label and 41% matched the label amount (Van Wagoner 2017). Lab analysis

The FDA warns that life-threatening reactions, including liver injuries needing hospital care, have occurred in people taking SARM products, and lists possible risks including heart attack or stroke, liver failure and infertility (FDA). Adverse event reports and single cases cannot prove that YK-11 caused a problem, but they are the only human safety data there are.

Hair loss, gyno and acne

None has been studied with YK-11. Because it activates the androgen receptor, the androgen-related effects seen with other SARMs and steroids are plausible, but they have not been measured. What is known across SARMs: YK-11 gyno, SARMs and hair loss, SARMs and acne and all SARMs side effects.

Does YK-11 suppress testosterone?

Not known. YK-11 activates the androgen receptor in cell tests (Kanno 2011), but we found no study in people or animals that measured testosterone, LH or FSH with it. Users often treat it as suppressive, and our YK-11 suppression page covers those reports. For what is known about recovery after androgen use and the PCT drugs that have been studied, see PCT after SARMs and the PCT and bloodwork planner.

Bloodwork

No study has tracked lab markers in people taking YK-11. Liver enzymes and bilirubin were raised in the case report where it was used with other SARMs (Lee 2023), and the markers that changed in trials of other SARMs are testosterone, FSH, SHBG and HDL cholesterol (Basaria 2013). Our SARMs bloodwork guide explains each test.

YK-11 dosage: what studies used

No human dose has ever been studied. Cell studies use concentrations in a dish, and the rat studies used doses per kilogram that do not translate to people. The only non-oral research use was a gel placed directly into a bone defect in rats (Wang 2025); there is no research on injecting YK-11. Products are sold by label strength: SwissChems, for example, sells YK-11 as 5 mg capsules. Our YK-11 dosage page explains what users report and what is known.

YK-11 half-life

Not measured in any published study. In an anti-doping study, no unchanged YK-11 appeared in urine after a dose; its breakdown products were traceable for more than 48 hours, and the unconjugated ones were gone within 24 hours (Piper 2018). Half-life figures quoted online do not come from a published study.

  • United States: not FDA-approved. In a December 2025 warning letter, the FDA called products sold as “YK-11” unapproved new drugs (FDA warning letter, 2025), and it says SARM products are unapproved drugs, not dietary supplements (FDA).
  • United Kingdom: UK Anti-Doping lists YK-11 (Myostine) among SARMs, says no SARM is approved for human use, and notes that SARMs are illegal to sell or advertise as food or in supplements (UK Anti-Doping).
  • Australia: not named separately, but SARMs as a class are prescription-only and possession without authority is illegal (Poisons Standard 2026).
  • Germany: named as an example SARM in the Anti-Doping Act’s annex (AntiDopG annex); trading in it for doping in sport, or possessing a non-small quantity for that purpose, is banned (AntiDopG §2).

More: are SARMs legal?

YK-11 in sport and drug tests

WADA names YK-11 as a SARM, banned at all times (WADA 2026). Labs test for its breakdown products because the intact drug does not show up in urine (Piper 2018), and a Los Angeles anti-doping lab reported finding it in a doping control sample (Sobolevsky 2024). See SARMs drug test.

YK-11 vs RAD-140, LGD-4033 and steroids

Compound Structure Human evidence Measured effect on lean mass
YK-11 Steroid None Not studied
LGD-4033 Nonsteroidal Two randomized trials +1.21 kg on 1 mg/day for 21 days (Basaria 2013)
RAD-140 Nonsteroidal One Phase 1 cancer trial Not measured in people (LoRusso 2022)
Anabolic steroids Steroid Compared in SARMs vs steroids

The practical difference is evidence: LGD-4033 has placebo-controlled human data showing both its effect and its suppression; YK-11 has none. Head-to-head pages: YK-11 vs RAD-140 and YK-11 vs LGD-4033, or use the compare tool.

Is YK-11 for beginners?

There is no human dosing or safety data for anyone, beginner or experienced. Of all the compounds sold as SARMs, it is one of the least studied: no human trial, no human pharmacokinetics, and human harms known only from case reports and adverse event reports. Our start here page covers the basics of the evidence and the risks.

YK-11 stacks

No study has tested YK-11 with anything. The human case reports all involve combinations: the liver-injury case with LGD-4033 and RAD-140 (Lee 2023) and the FDA product that also held an undeclared steroid (FDA). Stacking makes it impossible to tell which compound caused a problem. Our YK-11 stacks page covers common combinations, and the stack checker shows where documented risks overlap.

Buying YK-11: is it what the label says?

Products sold as SARMs are often mislabeled: in a test of 44 products, only 52% contained a SARM and 25% contained unlisted substances (Van Wagoner 2017), and the FDA’s YK-11 case involved a hidden steroid (FDA). Look for a lot-specific certificate of analysis and learn how to read a lab test. Our current pick is SwissChems, which publishes lot-specific lab reports; see our SwissChems review.

Bottom line

YK-11 is a steroid-based androgen receptor activator with an interesting cell study behind the “myostatin inhibitor” label and nothing behind the muscle claims in people. It has never been tested in a human trial, its half-life and its effect on testosterone are unknown, and the human safety record consists of a stroke linked to an FDA-tested product, a serious liver injury with other SARMs, and adverse event reports. In rats it harmed the hippocampus. It is banned in sport and cannot legally be sold as a supplement in the US or UK.

Charts

Half-life of YK-11 compared Elimination half-life in people, where measured (log scale; bars show the reported range). Values from different studies and routes are not directly comparable.
Half-life of YK-11 comparedIpamorelin: ~2 h; Enclomiphene: ~8–10 h; Ostarine: ~14–24 h; Clomiphene: ~5–24 h (No single value: enclomiphene part ~5–10 h; zuclomiphene part ~24 h with a very long tail (detectable for over a month)); LGD-4033: ~24–36 h (24–36 h); RAD-140: ~45 h; Anastrozole: ~2–2.1 days (~50 h); Tamoxifen: ~5–7 days (~5–7 days (tamoxifen); ~14 days (N-desmethyltamoxifen, main active metabolite)); CJC-1295: ~5.8–8.1 days (~6–8 days); YK-11: not established1 h3 h6 h12 h1 day3 days1 weekIpamorelinIpamorelin: ~2 h~2 hEnclomipheneEnclomiphene: ~8–10 h~8–10 hOstarineOstarine: ~14–24 h~14–24 hClomipheneClomiphene: ~5–24 h (No single value: enclomiphene part ~5–10 h; zuclomiphene part ~24 h with a very long tail (detectable for over a month))~5–24 hLGD-4033LGD-4033: ~24–36 h (24–36 h)~24–36 hRAD-140RAD-140: ~45 h~45 hAnastrozoleAnastrozole: ~2–2.1 days (~50 h)~2–2.1 daysTamoxifenTamoxifen: ~5–7 days (~5–7 days (tamoxifen); ~14 days (N-desmethyltamoxifen, main active metabolite))~5–7 daysCJC-1295CJC-1295: ~5.8–8.1 days (~6–8 days)~5.8–8.1 daysYK-11not established

Source: Sarmguide compound database; YK-11 value: Studies on the in vivo metabolism of the SARM YK11: Identification and characterization of metabolites potentially useful for doping controls (2018).

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More on YK-11

Frequently asked questions

Is YK-11 a SARM or a steroid?

A steroid that acts like a SARMEvidence: Lab

YK-11 has a steroid structure, but its discoverers found it only partly switches on the androgen receptor and called it a SARM. WADA lists it with the SARMs.

Read the full section

What does YK-11 do?

Unknown in peopleEvidence: Lab

In cells it partly activates the androgen receptor and, in mouse muscle cells, raised follistatin and muscle-building signals. In rats it helped repair a bone defect as a gel and, in other studies, harmed the hippocampus.

Read the full section

Is YK-11 a myostatin inhibitor?

Only shown in a lab dishEvidence: Lab

In mouse muscle cells, YK-11 raised follistatin, a protein that blocks myostatin, and that drove muscle-cell growth. No study has measured myostatin or follistatin in people taking it.

What results do users claim from YK-11?

Gains claimed; none measuredEvidence: User reports

Users report gains in size and strength, but no human study has tested YK-11 for muscle, strength or fat. Photos cannot separate its effect from training, diet, other drugs or a mislabeled product.

Read the full section

Has YK-11 been tested in humans?

NoEvidence: Limited

ClinicalTrials.gov lists no trials, and no published human treatment study was found. The research is in cells, rats and mice, plus anti-doping lab work.

Read the full section

What are the main risks of YK-11?

Stroke, liver injury reportsEvidence: Human data

FDA tested a product sold as YK-11 after a user had a stroke; it also held an undeclared steroid. A man who took YK-11 with LGD-4033 and RAD-140 developed serious liver injury, and in rats it caused oxidative stress and memory problems.

Read the full section

Does YK-11 cause hair loss?

Not studiedEvidence: Limited

It activates the androgen receptor, so androgen-related hair loss is plausible, but no study has measured it.

Read the full section

Does YK-11 suppress testosterone?

Not knownEvidence: Limited

It activates the androgen receptor in cell tests, but no study in people or animals has measured testosterone, LH or FSH with YK-11.

Read the full section

What is the half-life of YK-11?

Not measuredEvidence: Limited

In an anti-doping study, no unchanged YK-11 showed up in urine after a dose; its breakdown products were traceable for more than 48 hours.

Read the full section

What dose of YK-11 has been studied in people?

NoneEvidence: Limited

No human dosing study exists. Doses used in cells and rodents do not translate to people, and there is no research on injecting it.

Read the full section

Should beginners use YK-11?

No safety data for anyoneEvidence: Limited

It is one of the least studied compounds sold as a SARM: no human trial, no human pharmacokinetics, and human harms known only from case reports and adverse event reports.

Read the full section

Is YK-11 legal, and is it banned in sport?

Not approved; banned in sportEvidence: Law

The FDA calls products sold as YK-11 unapproved new drugs, and SARMs cannot legally be sold as food or supplements in the UK. WADA bans it at all times.

Read the full section

Sources

  1. (17α,20E)-17,20-[(1-methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna-4,20-diene-21-carboxylic acid methyl ester (YK11) is a partial agonist of the androgen receptor 2011 · PMID 21372378
  2. ClinicalTrials.gov search for 'YK-11' and 'YK11': no studies found (checked 30 October 2026) 2026
  3. FDA: Certain bodybuilding products put consumers at risk for heart attack, stroke, serious liver damage and more (content current as of 2 December 2025) 2025
  4. WADA: The Prohibited List (2026 List, in force from 1 January 2026) 2026
  5. PubChem: YK-11 (CID 119058028), names and synonyms 2026
  6. SARMs | UK Anti-Doping (supplement ingredient warning, updated 29 April 2026) 2026
  7. Mass spectrometric characterization of the selective androgen receptor modulator (SARM) YK-11 for doping control purposes 2017 · PMID 28440570
  8. YK11 induces oxidative stress and mitochondrial dysfunction in hippocampus: The interplay between a selective androgen receptor modulator (SARM) and exercise 2023 · PMID 37468001
  9. From gains to gaps? How Selective Androgen Receptor Modulator (SARM) YK11 impact hippocampal function: In silico, in vivo, and ex vivo perspectives 2024 · PMID 38521455
  10. Selective androgen receptor modulator, YK11, regulates myogenic differentiation of C2C12 myoblasts by follistatin expression 2013 · PMID 23995658
  11. Selective Androgen Receptor Modulator, YK11, Up-Regulates Osteoblastic Proliferation and Differentiation in MC3T3-E1 Cells 2018 · PMID 29491216
  12. YK11 promotes osteogenic differentiation of BMSCs and repair of bone defects 2025 · PMID 39660819
  13. Selective Androgen Receptor Modulator-Induced Liver Injury in Active Duty Male 2023 · PMID 35253885
  14. Selective androgen receptor modulator use and related adverse events including drug-induced liver injury: Analysis of suspected cases 2024 · PMID 38059982
  15. Chemical Composition and Labeling of Substances Marketed as Selective Androgen Receptor Modulators and Sold via the Internet 2017 · PMID 29183075
  16. The safety, pharmacokinetics, and effects of LGD-4033, a novel nonsteroidal oral, selective androgen receptor modulator, in healthy young men 2013 · PMID 22459616
  17. Studies on the in vivo metabolism of the SARM YK11: Identification and characterization of metabolites potentially useful for doping controls 2018 · PMID 30379415
  18. FDA Warning Letter to an online seller of products marketed as SARMs (MARCS-CMS 719645), 12 December 2025 2025
  19. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026 (F2026L00633) 2026
  20. Anlage zum Anti-Doping-Gesetz (AntiDopG), Germany (BGBl. 2023 I Nr. 67) 2023
  21. § 2 Anti-Doping-Gesetz (AntiDopG): Unerlaubter Umgang mit Dopingmitteln (Germany)
  22. Detection of selective androgen receptor modulator YK-11 in a doping control sample 2024 · PMID 37946705
  23. A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer 2022 · PMID 34565686
  24. Myostatin inhibitor YK11 as a preventative health supplement for bacterial sepsis 2021 · PMID 33588136