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RAD-140 + YK-11 RAD-140 (Testolone) plus YK-11 is a popular bodybuilding stack that pairs two selective androgen receptor modulators (SARMs) sought for rapid gains in muscle mass and strength [1]. RAD-140 is a potent nonsteroidal androgen receptor agonist designed to drive muscle growth with fewer of the prostate and hormonal effects of testosterone, while YK-11 is a steroidal SARM marketed as a myostatin-modulating muscle-builder [1][7]. Both are investigational research chemicals, not approved drugs, and both are banned in sport; importantly, RAD-140 has been linked in case reports to serious cardiac harm, so the stack carries real risk [1][2][3].
- Serious muscle growth potential
- High anabolic selectivity from RAD-140
- Myostatin brake released by YK-11
- Orally active
- Strength and recovery in user reports
- RAD-140 has been linked in medical case reports to serious heart problems in young users, including myocarditis and heart failure
- SARMs can suppress the body's natural testosterone production
Overview
RAD-140 plus YK-11 refers to a combination, or stack, of two selective androgen receptor modulators (SARMs) commonly sold together to bodybuilders and athletes seeking increases in muscle mass and strength [1]. SARMs are a class of compounds that bind the androgen receptor, the same receptor activated by testosterone, but were designed to favor anabolic effects in muscle and bone over the androgenic effects on the prostate and other tissues; despite active pharmaceutical research into conditions such as muscle wasting, cachexia, and sarcopenia, no SARM has received full clinical approval [1].
RAD-140, also called Testolone, is a nonsteroidal SARM originally developed as a potent, orally active androgen receptor agonist [1]. YK-11 is chemically different: it is a steroidal SARM built on a dihydrotestosterone-like steroid nucleus, and it is widely promoted to bodybuilders as a myostatin inhibitor, though that popular claim rests on limited laboratory research rather than human evidence [1][7]. Because the two compounds are thought to act on muscle through complementary androgen-receptor pathways, they are frequently combined in an effort to maximize gains, which is the basis for this paired entry.
Neither compound is approved by the United States Food and Drug Administration or any comparable regulator, and both have been on the World Anti-Doping Agency Prohibited List since SARMs were added in 2008, making them banned in essentially all competitive sport [1]. They are sold as research chemicals or mislabeled dietary supplements, and analytical surveys have repeatedly found SARMs including YK-11 present in supplements, sometimes undisclosed on the label and at widely varying concentrations; YK-11 in particular is chemically unstable [8]. They are usually encountered as capsules or as liquid solutions for oral use. The combination of unproven efficacy, no regulatory oversight, and documented serious adverse events makes this an especially high-risk category [1][8].
- Despite their muscle-building reputation, neither RAD-140 nor YK-11 has ever been approved as a medicine, and both are classified as investigational research chemicals.
- In a long-term study in mice, RAD-140 at 5 mg/kg failed to improve muscle strength and instead increased frailty and mortality risk.
- Multiple published case reports describe cholestatic liver injury with jaundice in young men who took RAD-140 for muscle growth, with recovery after they stopped the compound.
Mechanism
Both compounds in this stack act on the , the intracellular receptor through which testosterone and dihydrotestosterone stimulate muscle protein synthesis and growth. As selective androgen receptor modulators, they are intended to activate this receptor preferentially in muscle and bone, producing anabolic, muscle-building effects while causing fewer androgenic effects in tissues such as the prostate than anabolic steroids do [1]. RAD-140 (Testolone) is a nonsteroidal that binds the receptor and drives the gene-expression programs that increase muscle mass, and it is regarded as one of the more potent SARMs in this respect [1]. YK-11 is a steroidal SARM with a dihydrotestosterone-like structure; in addition to its androgen-receptor activity it is marketed as a myostatin inhibitor, meaning it is claimed to reduce the effect of myostatin, a natural brake on muscle growth, although this specific mechanism is supported only by limited in-vitro work and has not been demonstrated in humans [1][7]. Stacking the two is intended to combine complementary anabolic signals for greater muscle gain.
Critically, the anabolic promise of these compounds is not matched by evidence of safe benefit, and controlled data point in a cautionary direction. In a long-term study in mice, RAD-140 given at 5 mg/kg failed to improve muscle strength and instead increased frailty and mortality risk, suggesting that its effects may be more detrimental than beneficial rather than a clean anabolic gain [5]. No human clinical trials have established that either compound safely builds muscle, and their pharmacology in people is largely uncharacterized [1].
The most important mechanistic consideration is safety. Because androgen receptors are present in the heart and vasculature, potent androgen-receptor stimulation can affect cardiac tissue, and RAD-140 has been directly linked in medical case reports to serious cardiovascular events in young users, including acute myocarditis, myopericarditis, and even fatal heart failure [2][3][4]. Additional case reports describe severe events such as spontaneous splenic rupture in a user of RAD-140 together with the growth-hormone secretagogue MK-677 [6]. These harms, combined with the fact that supplement products frequently contain undisclosed or mislabeled SARMs, mean the real-world risk profile of a RAD-140 plus YK-11 stack is substantial and its benefits unproven [5][6][8].
receptor fingerprint
(RAD-140)potent agonist
HPG axis (LH / FSH / testosterone)suppresses
Myostatin (via follistatin, YK-11)suppresses
Follistatin (YK-11)upregulates
Dosingtypical ranges, not medical advice
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Safetyrisks and cautions, not medical advice
The combo has no human study behind it and stacks the risks of both compounds. RAD-140 strongly suppresses natural testosterone and has real-world reports of drug-induced liver injury; YK-11 adds its own liver concern given its methylated steroid-like structure. Expect lower HDL cholesterol and the need for a hormone-recovery plan afterward. Neither is approved, both are banned by WADA, and products are unregulated with uncertain content. The liver and hormonal load is the main reason to be cautious. Not for human use.
History
This stack pairs two separately developed research chemicals. RAD-140, also called Testolone, was discovered by the biopharmaceutical company Radius Health and first described in the scientific literature around 2011 as a potent nonsteroidal selective androgen receptor modulator intended for conditions such as muscle wasting and, in later work, hormone-receptor-positive breast cancer. YK-11 was synthesized by the Japanese researcher Yasuhiro Kanno and colleagues, also reported around 2011, as a steroidal SARM with a dihydrotestosterone-like structure that showed follistatin-related, myostatin-modulating activity in cell culture.
Neither compound has ever been approved for human use, and both entered the bodybuilding and research-chemical markets rather than clinical practice. The practice of stacking the two arose within fitness communities seeking combined anabolic signals, not from any formal drug-development program. Both agents are prohibited in sport by the World Anti-Doping Agency, and the pairing has no legitimate regulatory or clinical history.
Reputation
Within bodybuilding circles the RAD-140 and YK-11 stack has a strong reputation for producing rapid gains in muscle mass and strength, and RAD-140 in particular is often described by users as one of the more potent SARMs available. That enthusiasm, however, must be weighed against a sobering safety record and a striking absence of human evidence. No controlled clinical trials have shown that either compound safely builds muscle in people, and much of YK-11's myostatin-inhibiting reputation rests on limited in-vitro work rather than human data.
More seriously, RAD-140 has been linked in published medical case reports to drug-induced liver injury and to serious cardiovascular events in young users, and a long-term rodent study found it increased frailty and mortality rather than improving strength. Products sold as SARMs are also frequently mislabeled or adulterated. In honest terms, the anabolic appeal of this stack is real to its users, but its benefits remain unproven and its documented risks are substantial.
Subjective profileweighing the evidence above
Hard pass. RAD-140 has been linked in case reports to serious heart problems in young users and to drug-induced liver injury, YK-11 adds its own liver concern, and stacking them doubles that exposure with zero human study of the combination. Both suppress natural testosterone, and neither is approved or quality-controlled.
Resources
This entry is here for reference.
Research
- 2017first citedMass spectrometric characterization of the selective androgen receptor modulator (SARM) YK-11 f…
- 2024most active year3 papers
- 2026most recentSpontaneous Splenic Rupture in a Patient With Recent Use of Performance-Enhancing Compounds: A…
- 1.Detection of SARMs in doping control analysis.
- 2.Selective androgen receptor modulator abuse-induced heart failure: catastrophic effects of RAD-140 (Testolone).
- 3.Acute Myocarditis From the Use of Selective Androgen Receptor Modulator (SARM) RAD-140 (Testolone).
- 4.Myopericarditis Following Use of Selective Androgen Receptor Modifier "RAD-140".
- 5.RAD140 (Testolone) negatively impacts skeletal muscle adaptation, frailty status and mortality risk in female mice.
- 6.Spontaneous Splenic Rupture in a Patient With Recent Use of Performance-Enhancing Compounds: A Case Report and Literature Review.
- 7.Mass spectrometric characterization of the selective androgen receptor modulator (SARM) YK-11 for doping control purposes.
- 8.Development and validation of liquid chromatography-tandem mass spectrometry method for screening six selective androgen receptor modulators in dietary supplements.
- 9.RAD-140 Drug-Induced Liver Injury
- 10.Selective Androgen Receptor Modulators Leading to Liver Injury: A Case Report
10 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is in this blend?
RAD-140 (Testolone), a potent muscle-selective SARM, combined with YK-11, a SARM-like compound that blocks myostatin by raising follistatin.
Why stack them?
To push growth from two angles at once: strong androgen-receptor drive from RAD-140 plus release of the myostatin brake from YK-11.
How hard is it on hormones?
RAD-140 strongly suppresses testosterone on its own; adding a second androgen makes shutdown and recovery a bigger issue.
What about the liver?
Both carry liver concern, RAD-140 through case reports of liver injury and YK-11 through its steroid-like structure. Monitoring is important.
Is it approved or legal in sport?
No. Both are unapproved research chemicals and are banned by WADA. They are sold for laboratory use only.
Limitations of the evidence
- Both compounds are unapproved research chemicals with no established safe dose or long-term safety data
Adverse effects
- RAD-140 has been linked in medical case reports to serious heart problems in young users, including myocarditis and heart failure
- SARMs can suppress the body's natural testosterone production
Notes and cautions
- Products sold as SARMs are frequently mislabeled or contain undisclosed ingredients, and YK-11 is chemically unstable
- Both are banned in competitive sport and are not legal dietary ingredients