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Metandienone, more widely known by the former brand name Dianabol, is an orally active anabolic-androgenic steroid, a synthetic relative of the male hormone testosterone. Developed in the 1950s, it was among the first such steroids to be used widely by athletes and bodybuilders to build muscle and enhance performance. It has largely been withdrawn from legitimate medical use and is now encountered mainly as a non-medical performance-enhancing drug. In the United States and many other countries it is a controlled substance and is banned in competitive sport.
- Rapid mass and strength gains
- Classic oral cycle kickstarter
- Boosts nitrogen retention and protein synthesis
- Noticeable fullness and pump
- Can strain the liver, especially with prolonged oral use
- May raise cardiovascular risk and worsen cholesterol
- Can cause breast tissue growth in men and suppress natural hormone production
Overview
Metandienone, also spelled methandienone and marketed historically as methandrostenolone, is an anabolic-androgenic steroid derived from testosterone [2]. Its structure carries a methyl group at the 17-alpha position, a modification that lets the drug survive passage through the liver and remain active when taken by mouth, together with an added double bond in the steroid ring system [2][3]. The same 17-alpha-methyl group that makes it orally usable also contributes to its potential to harm the liver [1].
The compound was first synthesized in the mid-1950s by the pharmaceutical company Ciba in Switzerland and was introduced under the brand name Dianabol toward the end of that decade [3]. It became closely associated with weightlifting and bodybuilding and is often cited as the first anabolic steroid to see widespread use among competitive and recreational athletes [1]. Over the following decades, tightening regulation and doping bans pushed it out of legitimate supply channels in most countries [1].
Although anabolic steroids have some accepted medical roles, such as the treatment of certain hormone deficiencies and wasting conditions, metandienone itself is no longer marketed as an approved medicine in the United States and many other nations [1]. In practice it is used chiefly outside of medicine by people seeking to increase muscle size and strength, typically in amounts far above any that were once prescribed [1]. It is taken as an oral tablet.
Metandienone is a controlled substance in many jurisdictions; in the United States it is classified within Schedule III under anabolic steroid legislation, and it is prohibited in sport by the World Anti-Doping Agency [1]. Non-medical use has been linked to a broad range of adverse effects, including liver injury, unfavorable changes in cholesterol, cardiovascular strain, breast tissue growth in men, suppression of the body's own hormone production, and mood disturbances [1]. Because supply is illicit, product quality and content are frequently unreliable.
Mechanism
As an anabolic-androgenic steroid, metandienone acts as an of the [2]. Binding to this receptor in muscle and other tissues promotes protein synthesis and nitrogen retention, which underlies the gains in muscle mass and strength that the drug is used to pursue [2]. Like related steroids it can be converted by the enzyme aromatase into an estrogenic , so it also produces -like effects such as fluid retention and breast tissue growth in men [2]. Because it is only a weak substrate for 5-alpha-reductase, its androgenic actions are not strongly amplified in tissues where that enzyme is active [2]. Sustained use suppresses the hypothalamic-pituitary-gonadal axis, reducing the body's natural testosterone production [1].
receptor fingerprint
agonist
Muscle protein synthesis / nitrogen retentionraises
Aromatization ()increases
Safetyrisks and cautions, not medical advice
Dianabol (methandrostenone) is an oral 17-alpha-alkylated steroid and is hepatotoxic, capable of raising transaminases and causing cholestatic liver injury with extended use. It aromatizes readily, so estrogenic effects are prominent; gynecomastia, marked water retention, and elevated blood pressure are common without an aromatase inhibitor. It suppresses HDL and worsens the lipid profile, adding cardiovascular strain, and it strongly shuts down endogenous testosterone so post-cycle recovery is typically needed. Additional documented concerns include erythrocytosis, mood changes, and virilization risk in women.
Subjective profileweighing the evidence above
Effective and hard on you in equal measure. It is a 17-alkylated oral with documented liver injury, prominent estrogenic effects, a worsened lipid profile and complete suppression of your own testosterone. If it is used at all it needs bloodwork and supervision, and it is banned in any tested sport.
Resources
Don't even think about it.
Research
- 1974first citedUtilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placenta…
- 2014most active year4 papers
- 2019most recentHuman steroid biosynthesis, metabolism and excretion are differentially reflected by serum and…
- 1.Adverse health consequences of performance-enhancing drugs: an Endocrine Society scientific statement
- 2.Pharmacology of anabolic steroids
- 3.Metabolism of metandienone in man: identification and synthesis of conjugated excreted urinary metabolites, determination of excretion rates and gas chromatographic-mass spectrometric identification of bis-hydroxylated metabolites.
- 4.A comparative study of the effect of the dose and exposure duration of anabolic androgenic steroids on behavior, cholinergic regulation, and oxidative stress in rats
- 5.Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: A comprehensive review
- 6.Human hydroxysteroid dehydrogenases and pre-receptor regulation: insights into inhibitor design and evaluation
- 7.Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione
- 8.Structural basis for androgen specificity and oestrogen synthesis in human aromatase
- 9.Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta
- 10.Limitations of direct estradiol and testosterone immunoassay kits
- 11.Cross-reactivity of steroid hormone immunoassays: clinical significance and two-dimensional molecular similarity prediction
- 12.Limitations of direct immunoassays for measuring circulating estradiol levels in postmenopausal women and men in epidemiologic studies
17 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is Dianabol?
It is an oral anabolic steroid (methandrostenolone) historically used to rapidly build mass and strength.
Why is it called a kickstarter?
It is often used early in a cycle to produce fast gains while longer-acting compounds take effect.
Does it cause water retention?
Yes; it is known for noticeable water retention, which contributes to rapid but partly temporary size gains.
Is it hard on the liver?
As an oral 17-alpha-alkylated steroid, it can place strain on the liver.
Adverse effects
- Can strain the liver, especially with prolonged oral use
- May raise cardiovascular risk and worsen cholesterol
- Can cause breast tissue growth in men and suppress natural hormone production
Notes and cautions
- Banned in sport and a controlled substance in many countries