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Trenbolone



Trenbolone
Systematic (IUPAC) name
17β-Hydroxyestra-4,9,11-trien-3-one
Identifiers
CAS number 10161-33-8
ATC code  ?
PubChem 25015
Chemical data
Formula C18H22O2 
Mol. mass 270.37
Pharmacokinetic data
Bioavailability 100% (intramuscular)
Metabolism 5 months
Half life 3 days
Excretion Urinary:%
Therapeutic considerations
Pregnancy cat.

X

Legal status

Illegal (US)
Schedule IV (CA)

Routes Intramuscular

Trenbolone is a steroid used by veterinarians on livestock to increase muscle growth and appetite. To increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate (Finaplix Gold from Valopharm USA, TREMBLONA QV75 from Quality Vet, Mexico), Trenbolone enanthate or Trenbolone cyclohexylmethylcarbonate (Parabolan from Laboratoires NEGMA until 1997). Plasma lipases then remove the ester in the bloodstream leaving free trenbolone.

Illicit Use

No trenbolone compounds have been approved by the FDA for human use,[1] due to a lack of clinical applications and some potential negative side-effects.[2] It is classified as a Schedule III drug under the Controlled Substances Act. However, bodybuilders have been known to use the drug illicitly in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.

Trenbolone acetate is often referred to as "Fina" by illicit users, because injectible trenbolone acetate is often prepared from Finaplix H pellets, an ear-implant used by cattle ranchers to maintain the weight of cattle during shipping to slaughter.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone.[citation needed] Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it.

Short-term side effects include insomnia, high blood pressure, increased aggression, night sweats, and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.  

References

  1. ^ http://www.mesomorphosis.com/articles/collins/anabolic-steroids-and-the-law.htm
  2. ^ http://www.mesomorphosis.com/steroid-profiles/trenbolone.htm



 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Trenbolone". A list of authors is available in Wikipedia.
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