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Masteron is a brand name for drostanolone, a synthetic anabolic-androgenic steroid derived from dihydrotestosterone (DHT). Introduced around 1960 and once used medically, chiefly as a secondary treatment for breast cancer in women, it is now encountered mainly as a non-medical performance and physique-enhancing drug and is a controlled substance in many countries [1][2]. It is usually supplied as an injectable ester such as drostanolone propionate, and because it derives from DHT it cannot be converted into estrogen [1].
- Dry, hardening anabolic look
- Mild anti-estrogenic activity
- Classic contest-prep polish
- Minimal water retention
- Suppresses the body's own testosterone production
- Acne and accelerated male-pattern hair loss
- Unfavorable changes in cholesterol and added cardiovascular strain
- Virilizing effects in women, such as voice deepening and body hair growth
Overview
Drostanolone, sold under brand names including Masteron, Masteril, and Drolban, is an anabolic-androgenic steroid of the dihydrotestosterone family, structurally a form of DHT bearing an added methyl group. It was first described in the late 1950s and introduced for medical use around 1960 [2]. Historically its main licensed use was in the palliative treatment of advanced or metastatic breast cancer in women, where its androgenic action was employed to oppose tumor growth, an application later largely superseded by better-tolerated drugs. The unmodified compound was little used on its own; instead it was marketed as esters, principally drostanolone propionate and, less commonly, drostanolone enanthate, which prolong its action after injection.
As a DHT derivative, drostanolone has pharmacological features that set it apart from testosterone. It binds the androgen receptor and shows a relatively high anabolic-to-androgenic ratio in animal assays, and, importantly, it cannot be converted by the aromatase enzyme into estrogen, so it does not produce estrogen-related effects such as fluid retention or breast tissue growth in men [1]. It is not 17-alpha-alkylated, the structural change that makes many oral steroids hard on the liver, so it is given by injection and is not considered notably hepatotoxic by that mechanism [1]. These properties are the reason it found a specific niche in physique sport.
In non-medical use, drostanolone is favored by some bodybuilders and athletes, typically during cutting phases, for the lean, hardened muscular look it is believed to promote while sparing muscle during calorie restriction. Because it is widely misused, it is a frequent target of sports drug testing; in anti-doping analysis it has been described as one of the most commonly detected anabolic steroids [2]. Considerable analytical research has mapped its urinary metabolites to extend how long use can be detected, identifying long-lived glucuronide and sulfate metabolites that serve as markers of drostanolone misuse for weeks after administration [2][3][4]. It is prohibited in sport by anti-doping authorities.
Drostanolone is a controlled substance in many jurisdictions; in the United States it is a Schedule III controlled substance under the Controlled Substances Act, and it is similarly restricted elsewhere. Like other anabolic-androgenic steroids used at the high, non-therapeutic doses typical of physique enhancement, it carries health risks including acne, accelerated male-pattern hair loss, adverse changes in cholesterol, cardiovascular strain, suppression of the body's own testosterone production, and, in women, masculinizing effects such as voice deepening and increased body hair [1]. Because much non-medical supply is unregulated, product identity and purity are not assured.
Mechanism
Drostanolone produces its effects as an of the , the same receptor that mediates the actions of testosterone and dihydrotestosterone [1]. After the injected ester is cleaved to release the active steroid, drostanolone enters target cells and binds the ; the hormone-receptor complex then acts in the cell nucleus to change gene expression, increasing muscle protein synthesis and promoting nitrogen retention and other anabolic changes in skeletal muscle, while its androgenic activity drives masculinizing effects in tissues such as skin and hair follicles [1].
Two structural features shape its particular profile. Because it is a dihydrotestosterone derivative, drostanolone is not a substrate for aromatase and cannot be converted into estradiol; this accounts for the absence of estrogenic side effects and for the dry, non-water-retaining character that makes it attractive for use before competitions [1]. Because it lacks 17-alpha-alkylation, it is administered by injection rather than orally and does not cause the liver strain linked to alkylated oral steroids [1]. Like all exogenous androgens, it suppresses the hypothalamic-pituitary-gonadal axis through negative feedback, lowering the body's natural production of testosterone, and it is extensively metabolized into a range of glucuronide and sulfate conjugates that are excreted in urine and exploited for doping detection [1][2][3].
receptor fingerprint
agonist
(ER / aromatase)mild anti-estrogen
Aromatization (DHT-derived)does not aromatize
Safetyrisks and cautions, not medical advice
Masteron (drostanolone) is an injectable DHT-derived androgen that does not aromatize, so its risks skew androgenic and cardiovascular rather than estrogenic. It suppresses endogenous testosterone production, requiring recovery support after use, and its DHT backbone tends to accelerate male-pattern hair loss and acne in susceptible users, with a real virilization risk in women even at low doses. It worsens the lipid profile by lowering HDL and can raise blood pressure, contributing to cardiovascular strain typical of the class. Because it is not liver-toxic in injectable form, hepatic risk is low, but as an unapproved-for-humans compound its safety rests on anecdotal and pharmacologic reasoning rather than clinical trials. It is contraindicated in pregnancy, prostate or breast cancer, and pre-existing cardiovascular disease.
History
Masteron is the trade name for drostanolone propionate, an anabolic steroid created by Syntex Pharmaceuticals in 1959, the same period Syntex developed oxymetholone. On reaching the prescription market it was used almost exclusively to treat advanced, inoperable breast cancer in postmenopausal women, chosen for its comparatively low androgenic rating and reduced virilization risk. It was sold under names including Masteril, Drolban (under an Eli Lilly license), and Drostanolonum. Superseded by tamoxifen and other oncology options, its medical use faded, and Masteron became a widely used cutting and pre-contest steroid in bodybuilding, obtained largely through the grey market.
Subjective profileweighing the evidence above
A cosmetic drug with real costs. It gives a dry, hardened look with no water retention, and it also shuts down your own testosterone, accelerates male-pattern hair loss, lowers HDL and adds cardiovascular strain. Controlled in most countries, and virilizing in women even at low doses.
Resources
Don't even think about it.
Research
- 1974first citedUtilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placenta…
- 2022most recentAnabolic-androgenic steroids: How do they work and what are the risks?
- 1.Anabolic-androgenic steroids: How do they work and what are the risks?
- 2.New drostanolone metabolites in human urine by liquid chromatography time-of-flight tandem mass spectrometry and their application for doping control
- 3.Searching for new long-term urinary metabolites of metenolone and drostanolone using gas chromatography-mass spectrometry with a focus on non-hydrolysed sulfates
- 4.Enabling the inclusion of non-hydrolysed sulfated long term anabolic steroid metabolites in a screening for doping substances by means of gas chromatography quadrupole time-of-flight mass spectrometry
- 5.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
- 6.Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: A comprehensive review
- 7.Human hydroxysteroid dehydrogenases and pre-receptor regulation: insights into inhibitor design and evaluation
- 8.Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione
- 9.Structural basis for androgen specificity and oestrogen synthesis in human aromatase
- 10.Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta
10 listed here; entry last updated July 2026
Reviews
My notesprivate to this device
FAQ
Why is it called a cutting steroid?
It's valued for a dry, hardened look and works best when body fat is already low, making it popular for contest prep.
Does it really lower estrogen?
It has mild anti-estrogenic activity, but it's not a replacement for dedicated estrogen management on a cycle.
What are the main risks?
As an anabolic steroid it suppresses natural hormone production and carries androgenic risks like hair loss and acne; medical oversight matters.
Propionate vs enanthate?
Propionate acts faster and clears quicker, while enanthate is longer-acting, which affects injection frequency.
Adverse effects
- Suppresses the body's own testosterone production
- Acne and accelerated male-pattern hair loss
- Unfavorable changes in cholesterol and added cardiovascular strain
- Virilizing effects in women, such as voice deepening and body hair growth
Notes and cautions
- Sold mostly through unregulated channels, so purity is uncertain