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Epitestosterone

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Subject: 22R-Hydroxycholesterol, 20α,22R-Dihydroxycholesterol, 3α-Androstanediol, Cortodoxone, 5α-Androstane-3β,17β-diol
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Epitestosterone

Epitestosterone
Systematic (IUPAC) name
17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17- dodecahydrocyclopenta[a]phenanthren-3-one
Clinical data
Legal status
  • Schedule III
Identifiers
CAS Registry Number  N
ATC code None
PubChem CID:
DrugBank  YesY
ChemSpider  YesY
ChEBI  N
ChEMBL  YesY
Chemical data
Formula C19H28O2
Molecular mass 288.42
 N   

Epitestosterone is an endogenous antiandrogen[1] steroid, an epimer of the hormone testosterone. It is a weak competitive antagonist of the androgen receptor (AR) and a potent 5α-reductase inhibitor.[2]

Structurally, it differs from testosterone only in the configuration at the OH-bearing carbon, C17. Epitestosterone is believed to form in a similar way to testosterone; a 1993 study found that around 50% of epitestosterone production in human males can be ascribed to the testis,[3] although the exact pathway of its formation is still the subject of research. It has been shown to accumulate in mammary cyst fluid and in the prostate.[3] Epitestosterone levels are typically highest in young males; however, by adulthood, most healthy males exhibit a testosterone to epitestosterone ratio (T/E ratio) of about 1:1.[4]

Epitestosterone and testosterone

It has been shown that exogenous administration of testosterone does not affect levels of epitestosterone in the body. As a result, tests to determine the ratio of testosterone to epitestosterone in urine are used to find athletes who are doping.[5] A study of Australian athletes found that the mean T/E ratio in the study was 1.15:1.[6] Another study found that the max T/E ratio for the 95th percentile of athletes was 3.71:1, and the max T/E ratio for the 99th percentile was 5.25:1 [7]

Epitestosterone has not been shown to enhance athletic performance, although administration of epistestosterone can be used to mask a high level of testosterone if the standard T/E ratio test is used. As such, epitestosterone is banned by many sporting authorities as a masking agent for testosterone.

In 1996 the US athlete Mary Decker failed a T/E test with a T/E ratio of greater than 6, the limit in force at the time. She took the case to arbitration, arguing that birth control pills can cause false positives for the test, but the arbitration panel ruled against her.

On September 20, 2007 synthetic testosterone had been detected in the A sample, using the carbon isotope ratio test CIR. The presence of synthetic testosterone means that some of the testosterone in Landis’s body came from an external source and was not naturally produced by his own system. These results conflict with Landis's public speculation that it was a natural occurrence.[8] Landis originally denied the charges, but in 2010 Landis admitted to doping during much of his career,[9] but continued to adamantly deny taking testosterone that would have led to the positive test in the 2006 Tour de France.[10]

Notes

  1. ^
  2. ^
  3. ^ a b
  4. ^
  5. ^
  6. ^ http://doping-info.de/proceedings/proceedings_10_pdf/10_261.pdf
  7. ^ http://scienceblogs.com/purepedantry/upload/2006/07/te.jpg
  8. ^
  9. ^
  10. ^

External links

  • Landis has T/E ratio twice the tour limit


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