Clinical data
Trade names Agoviron, Android, Metandren, Oraviron, Oreton, Testovis, Testred, Virilon, others
Synonyms RU-24400; NSC-9701; 17α-Methyltestosterone; 17α-Methylandrost-4-en-17β-ol-3-one[1][2][3]
AHFS/ Monograph
  • AU: D
  • US: X (Contraindicated)
    Routes of
    By mouth, buccal, sublingual[4][5]
    Drug class Androgen; Anabolic steroid
    ATC code
    Legal status
    Legal status
    Pharmacokinetic data
    Bioavailability ~70%[6]
    Protein binding 98%[7]
    Metabolism Liver
    Elimination half-life ~3 hours[6]
    Duration of action 1–3 days[7]
    Excretion Urine: 90%[7]
    Feces: 6%[7][8]
    CAS Number
    PubChem CID
    ECHA InfoCard 100.000.333
    Chemical and physical data
    Formula C20H30O2
    Molar mass 302.451 g/mol
    3D model (JSmol)

    Methyltestosterone, sold under the brand names Android, Metandren, and Testred among others, is an androgen and anabolic steroid (AAS) medication which is used in the treatment of low testosterone levels in men, delayed puberty in boys, at low doses as a component of menopausal hormone therapy for menopausal symptoms like hot flashes, osteoporosis, and low sexual desire in women, and to treat breast cancer in women.[4][5][9][10][11] It is taken by mouth.[4][10][11]

    Side effects of methyltestosterone include symptoms of masculinization like acne, increased hair growth, voice changes, and increased sexual desire.[4] It can also cause estrogenic effects like fluid retention, breast tenderness, and breast enlargement in men and liver damage.[4] The drug is a synthetic androgen and anabolic steroid and hence is an agonist of the androgen receptor (AR), the biological target of androgens like testosterone and dihydrotestosterone (DHT).[4][12] It has moderate androgenic effects and moderate anabolic effects, which make it useful for producing masculinization.[4][13]

    Methyltestosterone was discovered in 1935 and was introduced for medical use in 1936.[14][15][16][17][4] It was synthesized shortly after the discovery of testosterone and was one of the first synthetic AAS to be developed.[14][15][16] In addition to its medical use, methyltestosterone is used to improve physique and performance, although it is not as commonly used as other AAS for such purposes due to its androgenic effects, estrogenic effects, and risk of liver damage.[4] The drug is a controlled substance in many countries and so non-medical use is generally illicit.[4]

    Medical uses

    Methyltestosterone is or has been used in the treatment of delayed puberty, hypogonadism, cryptorchidism, and erectile dysfunction in males, and in low doses to treat menopausal symptoms (specifically for osteoporosis, hot flashes, and to increase libido and energy), postpartum breast pain and engorgement, and breast cancer in women.[4][5][9] It is specifically approved in the United States for the treatment of hypogonadism and delayed puberty in males and the treatment of advanced inoperable breast cancer in females.[10] It was also approved in low doses in combination with esterified estrogens for the treatment of moderate to severe vasomotor symptoms associated with menopause in women in the United States, but this formulation was discontinued and hence is no longer used.[11]

    The dosages of methyltestosterone used are 10 to 50 mg/day in men for common medical uses like hypogonadism and delayed puberty as well as physique- and performance-enhancing purposes and 2.5 mg/day in women for menopausal symptoms.[4][18] Higher dosages of 50 to 200 mg/day have been used to treat women with inoperable breast cancer that has failed to respond to other therapies, although such dosages are associated with severe irreversible virilization.[4][18]

    Non-medical uses

    Methyltestosterone is used for physique- and performance-enhancing purposes by competitive athletes, bodybuilders, and powerlifters, although it is not commonly used relative to other AAS for such purposes.[4]


    Methyltestosterone should be used with caution in women and children, as it can cause irreversible virilization.[4] Due to its estrogenicity, methyltestosterone can also accelerate epiphyseal closure and thereby produce short stature in children and adolescents.[4] It can worsen symptoms in men with benign prostatic hyperplasia.[4] Methyltestosterone should not be used in men with prostate cancer, as androgens can accelerate tumor progression.[4] The drug should be used with caution in patients with pre-existing hepatotoxicity, due to its own potential for hepatotoxicity.[4]

    Side effects

    Adverse effects of methyltestosterone include androgenic side effects like oily skin, acne, seborrhea, increased facial/body hair growth, scalp hair loss, increased aggressiveness and sex drive, and spontaneous erections, as well as estrogenic side effects like breast tenderness, gynecomastia, fluid retention, and edema.[4][19] In women, methyltestosterone can cause partially irreversible virilization, for instance voice deepening, hirsutism, clitoromegaly, breast atrophy, and muscle hypertrophy, as well as menstrual disturbances and reversible infertility.[4][19] In men, the drug may also cause hypogonadism, testicular atrophy, and reversible infertility at sufficiently high dosages.[4][19]

    Methyltestosterone can sometimes cause hepatotoxicity, for instance elevated liver enzymes, cholestatic jaundice, peliosis hepatis, hepatomas, and hepatocellular carcinoma, with extended use.[4][19][20] It can also have adverse effects on the cardiovascular system.[4] AAS like methyltestosterone stimulate erythropoiesis (red blood cell production) and increase hematocrit levels and at high dosages can cause polycythemia (overproduction of red blood cells), which can greatly increase the risk of thrombic events such as embolism and stroke.[4] With long-term treatment, AAS can increase the risk of benign prostatic hyperplasia and prostate cancer.[4] Violent and even homicidal behavior, hypomania/mania, depression, suicidality, delusions, and psychosis have all been associated with very high dosages of AAS.[21]


    Aromatase inhibitors can be used to reduce or prevent the estrogenic effects of methyltestosterone and 5α-reductase inhibitors can be used to prevent its potentiation in so-called "androgenic" tissues and thereby improve its ratio of anabolic to androgenic activity and reduce its rate of androgenic side effects.[4] Antiandrogens like bicalutamide and cyproterone acetate can block both the anabolic and androgenic effects of AAS like methyltestosterone.



    As an AAS, methyltestosterone is an agonist of the androgen receptor (AR), similarly to androgens like testosterone and dihydrotestosterone (DHT).[4][19] It is a substrate for 5α-reductase like testosterone, and so is potentiated analogously in so-called "androgenic" tissues like the skin, hair follicles, and prostate gland via transformation into the more potent AR agonist mestanolone (17α-methyl-DHT).[4][19] As such, methyltestosterone has a relatively low ratio of anabolic to androgenic activity, with a similar ratio to that of testosterone (close to 1:1), and this makes it among the most androgenic AAS.[4][19] Due to efficient aromatization into the potent and metabolism-resistant estrogen methylestradiol (17α-methylestradiol), methyltestosterone has relatively high estrogenicity and hence potential for estrogenic side effects such as gynecomastia and fluid retention.[15][22] The drug possesses negligible progestogenic activity.[4][19]

    Due to its combined disadvantages of a relatively poor ratio of anabolic to androgenic activity, unusually high estrogenicity, and the potential for hepatotoxicity (as with other 17α-alkylated AAS), methyltestosterone has not been used as commonly as many other AAS either in medicine or for physique- or performance-enhancing purposes.[4]


    Methyltestosterone has dramatically improved oral bioavailability and metabolic stability relative to testosterone.[4][19] This difference is due to the C17α methyl group, which results in steric hindrance and prevents metabolism.[4][19] The oral bioavailability of methyltestosterone is about 70%, and it is well-absorbed from the gastrointestinal tract.[6] Methyltestosterone can also be taken buccally or sublingually.[4][6] Although effective orally, methyltestosterone is more effective by these parenteral routes, which are said to approximately double its bioavailability.[4][6] Although methyltestosterone is much more potent than testosterone by the oral route, it still has relatively low potency among AAS when taken by mouth; the recommended dosage of methyltestosterone for androgen replacement in men is more than 10 times lower than that of the closely related AAS fluoxymesterone (25 mg/day buccally and 2 mg/day orally, respectively).[13] It is highly protein-bound, by approximately 98%.[7] The drug has low but significant affinity for human serum sex hormone-binding globulin (SHBG), about 25% of that of testosterone and 5% of that of DHT.[4][23] The biological half-life of methyltestosterone is approximately 3 hours (range 2.5–3.5 hours).[6][8] The duration of action of methyltestosterone is said to be 1 to 3 days, and is described as relatively short among AAS.[7][24] It is excreted 90% in the urine as conjugates and other metabolites, and 6% in feces.[7]


    Methyltestosterone, also known as 17α-methyltestosterone or as 17α-methylandrost-4-en-17β-ol-3-one, is a synthetic, 17α-alkylated androstane steroid and a derivative of testosterone differing from it only in the presence of a methyl group at the C17α position.[1][2][4] Close synthetic relatives of methyltestosterone include metandienone (17α-methyl-δ1-testosterone) and fluoxymesterone (9α-fluoro-11β-hydroxy-17α-methyltestosterone).[4][19]


    Methyltestosterone and ethyltestosterone (17α-ethyltestosterone) are the parent structures of all 17α-alkylated AAS. Major 17α-alkylated AAS include the testosterone derivatives fluoxymesterone, metandienone (methandrostenolone), and methyltestosterone and the DHT derivatives oxandrolone, oxymetholone, and stanozolol.[4][19]


    A chemical synthesis of methyltestosterone from dehydroepiandrosterone (DHEA) with methandriol as an intermediate proceeds as follows:[25][26]


    Methyltestosterone was first synthesized in 1935 along with methandriol and mestanolone.[27][28][14][15][16] It was the second synthetic AAS to be developed, following mesterolone (1α-methyl-DHT) in 1934, and was the first 17α-alkylated AAS to be synthesized.[14][15][16] The drug was introduced for medical use in 1936.[17][4]

    Society and culture

    Generic names

    Methyltestosterone is the INN, USAN, USP, BAN, and JAN of the drug and its generic name in English and Japanese, while méthyltestostérone is its DCF and French name and metiltestosterone is its DCIT and Italian name.[1][2][29][3] The generic name of the drug is methyltestosterone in Latin, methyltestosteron in German, and metiltestosterona in Spanish.[1][2][3] Methyltestosterone is also known by its former developmental code name NSC-9701.[29][3]

    Brand names

    Brand names under which methyltestosterone is or has been marketed for medical use include Afro, Agovirin, Android, Androral, Mesteron, Metandren, Methitest, Methyltestosterone, Methyl Testosterone, Oraviron, Oreton, Oreton Methyl, Testormon, Testovis, Testred, and Virilon, among others.[1][2][3][30]

    With an estrogen

    Methyltestosterone is available at a low-dose in combination with esterified estrogens for the treatment of menopausal symptoms like hot flashes in women under the brand names Covaryx, Essian, Estratest, Menogen, and Syntest.[4][31]


    United States

    Although it is not commonly used, methyltestosterone is one of the few AAS that remains available for medical use in the United States.[4][30] The others are testosterone, testosterone cypionate, testosterone enanthate, testosterone undecanoate, nandrolone decanoate, oxandrolone, oxymetholone, and fluoxymesterone.[30]

    Other countries

    Methyltestosterone has also been marketed in many other countries throughout the world.[1][2][3][4][32][33]

    Methyltestosterone, along with other AAS, is a schedule III controlled substance in the United States under the Controlled Substances Act and a schedule IV controlled substance in Canada under the Controlled Drugs and Substances Act.[34][35]


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    Further reading

    • Phillips EH, Ryan S, Ferrari R, Green C (2003). "Estratest and Estratest HS (esterified estrogens and methyltestosterone) therapy: a summary of safety surveillance data, January 1989 to August 2002". Clin Ther. 25 (12): 3027–43. doi:10.1016/s0149-2918(03)90090-7. PMID 14749144. 
    • Kabat GC, Kamensky V, Heo M, Bea JW, Hou L, Lane DS, Liu S, Qi L, Simon MS, Wactawski-Wende J, Rohan TE (2014). "Combined conjugated esterified estrogen plus methyltestosterone supplementation and risk of breast cancer in postmenopausal women". Maturitas. 79 (1): 70–6. doi:10.1016/j.maturitas.2014.06.006. PMID 25011395. 
    • El-Desoky el-SI, Reyad M, Afsah EM, Dawidar AA (2016). "Synthesis and chemical reactions of the steroidal hormone 17α-methyltestosterone". Steroids. 105: 68–95. doi:10.1016/j.steroids.2015.11.004. PMID 26639430. 

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