Clinical data | |
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Trade names | Anadrol, Anapolon, others |
Other names | CI-406; NSC-26198; 2-Hydroxymethylene-17α-methyl-4,5α-dihydrotestosterone; 2-Hydroxymethylene-17α-methyl-DHT; 2-Hydroxymethylene-17α-methyl-5α-androstan-17β-ol-3-one |
AHFS/Drugs.com | Consumer Drug Information |
Pregnancy category |
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Dependence liability | Moderate [1] |
Addiction liability | Moderate [1] |
Routes of administration | By mouth |
Drug class | Androgen; Anabolic steroid |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | Well-absorbed[3] |
Metabolism | Liver[3][4] |
Elimination half-life | Unknown[4] |
Excretion | Urine[3][4] |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.006.454 |
Chemical and physical data | |
Formula | C21H32O3 |
Molar mass | 332.484 g·mol−1 |
3D model (JSmol) | |
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(what is this?) (verify) |
Oxymetholone, sold under the brand names Anadrol and Anapolon among others, is an androgen and anabolic steroid (AAS) medication which is used primarily in the treatment of anemia.[5][6] It is also used to treat osteoporosis, HIV/AIDS wasting syndrome, and to promote weight gain[7] and muscle growth in certain situations.[5] It is taken by mouth.[5][6]
Side effects of oxymetholone include increased sexual desire as well as symptoms of masculinization like acne, increased hair growth, and voice changes.[5] It can also cause liver damage.[5][6] 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).[5][8] It has strong anabolic effects and weak androgenic effects.[5]
Oxymetholone was first prescribed in 1959 and was introduced for medical use but shortly after was discontinued due its high lipid toxicity in the year 1961.[5][9][10][11] It is used mostly in the United States.[5][12] In addition to its medical use, oxymetholone is used to improve physique and performance.[5] The drug is a controlled substance in many countries and so non-medical use is generally illicit.[5]
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