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MK-3984 is an experimental selective androgen receptor modulator (SARM) developed by Merck. Like other SARMs it was designed to switch on the androgen receptor selectively in muscle and bone while largely sparing tissues such as the prostate, with the goal of treating conditions like muscle wasting and osteoporosis. It never reached clinical use, its development was discontinued, and today it is encountered mainly as a research chemical.
- Claimed muscle support (unverified)
- Claimed recovery support (unverified)
- Claimed energy (unverified)
Overview
MK-3984 is a nonsteroidal selective androgen receptor modulator (SARM). It has the molecular formula C17H12F7NO2 and a molar mass of roughly 395, is registered under CAS number 871325-55-2, and carries the systematic name (2R)-3,3,3-trifluoro-N-[[2-fluoro-5-(trifluoromethyl)phenyl]methyl]-2-hydroxy-2-phenylpropanamide. The MK prefix marks it as a compound from Merck Sharp and Dohme.
SARMs are a class of drugs that bind the androgen receptor but act with tissue selectivity: they behave as anabolic agonists in muscle and bone while producing much weaker androgenic activity in tissues such as the prostate and skin. Because they are orally active and are not converted to estrogen, they were pursued as a way to gain the muscle- and bone-building benefits of androgens with fewer side effects than testosterone. MK-3984 was one of a number of SARM candidates explored for indications including the muscle wasting that accompanies cancer and the bone loss of osteoporosis [1][2].
Despite this interest, MK-3984 did not advance to approved medical use and its development program was ended. It has no license as a medicine in any country. Like other discontinued SARMs it has surfaced in the gray-market supplement trade, where it is sold as a research chemical rather than a regulated drug, and strong performance claims about it are not backed by clinical evidence.
Because SARMs are banned in competitive sport, MK-3984 has more recently drawn attention from anti-doping science. A 2026 study mapped its metabolic breakdown products in a zebrafish model in order to establish markers for detecting its use in athletes [3]. Human safety and efficacy data for the compound remain absent.
Mechanism
MK-3984 works by binding the and acting as a tissue-selective modulator of it. In anabolic tissues such as skeletal muscle and bone it behaves largely as an , switching on androgen receptor-driven gene transcription that promotes protein synthesis and bone formation, while in classically androgenic tissues such as the prostate and skin it acts as a weaker or partial agonist, which is the property intended to reduce the side effects associated with testosterone [1][2]. Being a nonsteroidal molecule, it is not aromatized to . Its detailed human pharmacokinetics were never established; the most thorough modern characterization concerns the metabolites it forms, studied to enable detection of its misuse in sport [3].
receptor fingerprint
Unknown molecular targetunverified
Muscle anabolism (claimed)unverified
Recovery pathways (claimed)unverified
Dosingtypical ranges, not medical advice
interested in protocols and clinical dosages? make an account to see them! ^_^
Safetyrisks and cautions, not medical advice
Because there is no reliable safety data, MK-3984 should be considered unknown and potentially risky. Gray-market products may be mislabeled or contaminated. Using it is not advisable, and anyone considering it should recognize they are essentially self-experimenting with an uncharacterized compound.
Subjective profileweighing the evidence above
Not enough verified information to recommend; it is an unvetted research chemical and best avoided.
Resources
This entry is here for reference.
Research
- 2013first citedSelective androgen receptor modulators for the prevention and treatment of muscle wasting assoc…
- 2026most recentMetabolic profiles of MK-3984 (SARM) in zebrafish using ultra high performance liquid chromatog…
- 1.Overview of the development of selective androgen receptor modulators (SARMs) as pharmacological treatment for osteoporosis (1998-2021)
- 2.Selective androgen receptor modulators for the prevention and treatment of muscle wasting associated with cancer
- 3.Metabolic profiles of MK-3984 (SARM) in zebrafish using ultra high performance liquid chromatography Q extractive HF hybrid quadrupole orbitrap mass spectrometry (UPLC-QE-HF-MS) for doping control
3 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is MK-3984?
It's an obscure research code with little verified public pharmacology; reliable data on its target and effects is essentially absent.
Is it a SARM?
It is sometimes marketed near SARM-like products, but I couldn't confirm its class or mechanism from credible sources.
Is it safe?
There's no reliable safety data, so it should be treated as unknown and potentially risky.
What dose should I take?
There's no evidence-based dose; using it at all is not advisable.
Why so little information?
Some codes circulate in gray markets without ever being properly studied or published, which is a warning sign.
Limitations of the evidence
- No human safety data established
Notes and cautions
- Androgen-related effects possible in principle
- Prohibited in competitive sport
- Purity and identity uncertain when sold as a research chemical