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18-Methyltestosterone
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    18-Methyltestosterone

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    18-Methyltestosterone
    18-Methyltestosterone.svg
    Clinical data
    Other names 18-MT; 18-Methylandrost-4-en-17β-ol-3-one; 13β-Ethyl-17β-hydroxy-18-norandrost-4-en-3-one
    Drug class Androgen; Anabolic steroid
    Identifiers
    • (8R,9S,10R,13S,14S,17S)-13-ethyl-17-hydroxy-10-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
    CAS Number
    PubChem CID
    UNII
    Chemical and physical data
    Formula C20H30O2
    Molar mass 302.458 g·mol−1
    3D model (JSmol)
    • CC[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=CC(=O)CC[C@]34C
    • InChI=1S/C20H30O2/c1-3-20-11-9-16-15(17(20)6-7-18(20)22)5-4-13-12-14(21)8-10-19(13,16)2/h12,15-18,22H,3-11H2,1-2H3/t15-,16+,17+,18+,19+,20+/m1/s1
    • Key:VIDBKWVIQCRYHG-HLXURNFRSA-N

    18-Methyltestosterone (18-MT) is an androgen/anabolic steroid (AAS) which was never marketed. Along with 19-nortestosterone (nandrolone) and 17α-ethynyltestosterone (ethisterone), it is a parent structure of a number of progestogens and AAS. These include the progestogens levonorgestrel (17α-ethynyl-18-methyl-19-nortestosterone) and its derivatives (e.g., desogestrel, gestodene, norgestimate, gestrinone) as well as AAS such as norboletone (17α-ethyl-18-methyl-19-nortestosterone) and tetrahydrogestrinone (THG; δ9,11-17α-ethyl-18-methyl-19-nortestosterone).

    See also



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