China 99% Muscle Establishment Anabolic Steroid Powder Metribolone CAS 965-93-5
Methyltrienone is a steroid compound used for muscle establishment and fat burning.Trenbolone is a steroid used by veterinarians to increase muscle growth and appetite. In order to increase its effective half-life, tebufen is not used in the unrefined form, but as an ester derivative such as trenbolone acetate, trenbolone enanthate or dibbylcyclohexylmethyl Carbonate (Parabolan) administration. Then the plasma lipase cleaves the ester groups in the bloodstream, leaving the free tibolone.
Methyltrienolone (methyltrienolone aka R1881) is a potent, non-aromatizable androgen that is structurally similar to trenbolone and has been referred to as "oral tren." Methyltrienolone binds strongly to the androgen receptor (AR) and is a more potent agonist (activator) of the androgen receptor than is DHT.
17a-methyltrienolone is listed at 30,000 times more anabolic than methyltestosterone according to Julius Vida in "Androgens and Anabolic Agents: Chemistry and Pharmacology." Effective dosages begin at only 25mcg.
Steroid experts William Llewellyn and Patrick Arnold have each called methyltrienolone one of the "most powerful" anabolic steroids ever created. It is also one of the most hepatotoxic androgens ever produced. Originally developed by Roussell-UCLAF during the 1960s, the hepatoxicity of Metribolo prevented its commercial release. Bill Roberts likened the toxicity of methyltrienolone to that of taking high dosages
of Anadrol combined with high dosages of Halotestin concurrently.
According to Patrick Arnold, several athletes used methyltrienolone in the 1990s and were able to successfully pass doping controls looking for methyltrienolone due to the very small quantities of the steroid required for performance enhancing effects. He was somewhat surprised that methyltrienolone was detected by drug testers in the Greek steroid scandal suggesting that anti-doping tests have improved for the substance; 11 Greek weighlifters and 4 Greek track and field athletes tested positive for
methyltrienolone prior to the 2008 Beijing Olympic Games.
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Methyltrienol is a modified form of nandrolone. The difference is that: 1) adding methyl groups at 17 wells to protect the hormones during oral administration, and 2) introducing double bonds at carbon and 9 and 11 to increase their binding affinity and slow down their metabolism. The resulting steroid is significantly more effective than its nandrolone base and shows a longer half-life and a lower affinity for serum binding
proteins compared to that. Methyltrienol is different from fossilone chemistry except that methyl is added to c-17 only. However, this change significantly changes the activity of the methylenetriol, so that the agent should not be simply considered to be an oral form of chemokines.
Methyltrienolone (Methyl Trenbolone, MT, Tren Tabs, Metribolone, R1881) is a very potent, non-aromatizing androgen.(1) Methyltrienolone binds so strongly to the AR (androgen receptor) that it has been used as a photoaffinity label for the androgen receptor.(2) In other words, this stuff binds onto the AR so strongly that it is pretty much the benchmark in studies on other androgens to measure how strongly they bind to the AR. If you've read the profile on Trenbolone acetate (TA), you'll note that it said TA is the most potent injectable weapon in our arsenal with regards to ability to bind to the Androgen Receptor. That's still true, because methyltrienolone is not injectable.
It is simply the oral version of TA, which means it is Trenbolone which has undergone modification to become orally active, via the addition of a 17-alpha-methyl group.
Methyltrienolone would probably be best used as part of a cutting cycle, stacked with some injectables (testosterone, etc...), but absolutely no other orals. Methyl Trenbolone is just too hepatotoxic.(10) Methyl Tren was originally developed by Roussell-UCLAF during the 1960s, then explored further by Negma, the French company who brought Parabolan (trenbolone hexahydrobenzylcarbonate) to the market (and then discontinued it). Methyl Tren was never pushed for approval as a commercially released drug, since the original studies showed it to be highly toxic.
Studies have shown that taking oral anabolic steroids and foods may reduce their bioavailability.630 This is caused by the lipid-soluble properties of steroid hormones, which may allow some drugs to dissolve undigested dietary fats and reduce their absorption from the gastrointestinal tract Road. In order to maximize the use of methyl trienol should be taken in fasting.
Due to unacceptable levels of hepatotoxicity, methotrienol is no longer used in clinical medicine. For the same reason, this drug is usually not recommended for physical or performance enhancement purposes. Those who absolutely insist on using them need to pay great attention to the level of liver toxicity. At least routine blood tests should be performed to ensure that the medicament does not cause damage. The
duration of the drug should also be very limited, preferably for more than 4 weeks.
The relative potency of methyltrienol is very high, requiring only 0.5 mg of dose per day. Its effective and tolerable range is generally considered to be 0.5 to 2 mg per day. Every day 20-30 mg of Dianabol type dose is totally unimaginable and should not be tried. Again, this is an extremely toxic steroid, and all good advice will say to avoid it. Many of the commercially available steroids will be safer for anyone.
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