Mestanolone
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| Clinical data | |
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| Pregnancy category |
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| Routes of administration | Oral |
| Legal status | |
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| Pharmacokinetic data | |
| Bioavailability | 99% oral |
| Protein binding | yes |
| Metabolism | Hepatic |
| Elimination half-life | ? |
| Excretion | Renal |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| E number | {{#property:P628}} |
| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C20H32O2 |
| Molar mass | 304.467 g/mol |
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Mestanolone is the 17α-methylated version of dihydrotestosterone (DHT).[1] The systematic name of mestanolone is: 17β-hydroxy-17α-methylandrost-3-one.[2] It is an orally bioavailable androgenic steroid that is highly androgenic while only slightly anabolic. It is incapable of aromatization and is not an agonist of the progesterone receptor.
References
- ↑ CTD (2007). "Chemicals: mestanolone". CTD - Comparative Toxicogenomics Database. Unknown parameter
|accessyear=ignored (|access-date=suggested) (help); Unknown parameter|accessmonthday=ignored (help) - ↑ Biology Online.org (2007). "mestanolone". Biology Online.org. Unknown parameter
|accessyear=ignored (|access-date=suggested) (help); Unknown parameter|accessmonthday=ignored (help)
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