Silandrone
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| Silandrone | |
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| IUPAC name Silandrone | |
| Systematic name 2,15-Dimethyl-14-[(trimethylsilyl)oxy]tetracyclo[8.7.0.02,7.011,15]heptadec-6-en-5-one | |
| Other names O-Trimethylsilyltestosterone | |
| Identifiers | |
| CAS number | 5055-42-5 (1S,2R,10R,11S,14S,15S)  |
| PubChem | 521285, 6432482 (14S), 10316503 (1S,2R,11S,14S,15S), 12731048 (1S,2R,10R,11S,14R,15S), 68627 (1S,2R,10R,11S,14S,15S) |
| ChemSpider | 61886 (1S,2R,10R,11S,14S,15S) |
| EC number | 225-755-5 |
| KEGG | D05837 |
| ChEBI | CHEBI:607921 |
| Jmol-3D images | {{#if:O=C4\C=C2/[C@]([C@H]1CC[C@@]3([C@@H](O[Si](C)(C)C)CC[C@H]3[C@@H]1CC2)C)(C)CC4|Image 1 |
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| Properties | |
| Molecular formula | C22H36O2Si |
| Molar mass | 360.61 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
Silandrone also known as SC-16148 is an anabolic steroid that was developed at G. D. Searle & Company. Silandrone has a very long duration of action and high potency.[1][2]
References
- ↑ Saunders FJ (November 1966). "A singularly long-acting ether of testosterone". Proc. Soc. Exp. Biol. Med. 123 (2): 303–4. doi:10.3181/00379727-123-31472. PMID 5951069.
- ↑ Le Boeuf BJ, Allen JL (1970). "Prolonged reinstatement of sexual behavior in castrated male rats with an ether of testosterone, SC-16148". Hormones and Behavior 1 (2). doi:10.1016/0018-506X(70)90004-8.
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