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Clinical data | |
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Routes of administration |
Oral, intramuscular injection, subcutaneous injection |
Identifiers | |
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Synonyms | Testosterone 17β-trimethylsilyl ether; Testosterone O-trimethylsilyl ether; 17β-Trimethylsilyltestosterone; O-Trimethylsilyltestosterone; 17β-(trimethylsiloxy)androst-4-en-3-one; SC-16148; NSC-95147 |
CAS Number | 5055-42-5 |
PubChem (CID) | 68627 |
ChemSpider |
61886 ![]() |
UNII |
YY7GL3CCE9 ![]() |
KEGG | D05837 |
ChEBI | CHEBI:607921 |
ChEMBL | CHEMBL485687 |
ECHA InfoCard | 100.023.414 |
Chemical and physical data | |
Formula | C22H36O2Si |
Molar mass | 360.613 g/mol |
3D model (Jmol) | Interactive image |
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Silandrone (INN, USAN) (developmental code names SC-16148, NSC-95147), also known as testosterone 17β-trimethylsilyl ether or 17β-trimethylsilyltestosterone, as well as 17β-(trimethylsiloxy)androst-4-en-3-one, is a synthetic anabolic-androgenic steroid (AAS) and an androgen ether – specifically, the 17β-trimethylsilyl ether of testosterone – which was developed by the G. D. Searle & Company in the 1960s but was never marketed. It has a very long duration of action when given via subcutaneous or intramuscular injection as well as, notably, significantly greater potency than that of testosterone propionate. In addition, it is notable that silandrone, unlike testosterone and most esters of testosterone like testosterone propionate, is orally active.