Methyltrienolone (MT) is a very powerful, low-toxicity, non-aromatizing steroid. Ok. Let us go over those three topics again. To begin with, MT is really powerful. It binds so strongly to the AR (androgen receptor) that it is often used to assess how strongly other androgens bind. In other words, this substance binds so tightly to the AR receptor that it is very much the gold standard for that property. If you read my Trenbolone Acetate (TA) profile, you will notice that I said that TA is the most powerful injectable weapon in our armory in terms of capacity to bind to the Androgen Receptor. That remains true since this specific drug is not in our arsenal and cannot be injected… it is merely the oral form of TA (i.e. it is Trenbolone which has undergone modification to become orally active, via the addition of a 17-alpha-methyl group).
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So, why is it critical that this material bonds so firmly to the AR? Androgen Receptors are located in both fat and muscle cells; they operate on the AR in muscle cells to stimulate development, and on the AR in fat cells to influence fat burning. The more androgen binds to the A.R, the greater the lipolytic (fat burning) action on adipose (fat)tissue. Unfortunately, a strong binding does not inherently elicit the highest potential anabolic response, nor does a poor binding induce a weak anabolic response. Anadrol (oxymetholone), for example, has the lowest bind to the AR conceivable (too low to test) yet causes a significant anabolic response.
Dianabol is a relatively low-dose anabolic stimulant with a strong anabolic effect. ARs may be present in both muscle and adipose tissue. When the AR of a muscle is activated, it might cause hypertrophy. Fat is lost when an adipose tissue AR is triggered by multiple associated pathways. This is an oversimplification. Whatever. All we need to know is that when a steroid attaches to the AR, it develops muscle while burning fat. And a steroid that binds strongly to the AR will promote a lot of muscle synthesis while also burning a lot of fat.
Trenbolone is an excellent illustration of this. And, since I brought up Trenbolone, it is worth noting that MT is essentially a 17aa (oral) form of (injectable) Trenbolone. However, AR binding and stimulation are not the sole mechanisms that induce anabolism. It should be noted that Dbol has a very poor AR binding ability, while A50 has an AR binding capacity that is too low to test! However, both are very strong oral steroids. So, although crucial, AR binding/stimulation is not the be-all and end-all of anabolism, while it is a component of it. Do not be misled by the anabolic/androgenic ratio of this (or any other steroid). The anabolic/androgenic ratio of MT suggests that it has 120(+) times the anabolic and 60(+) times the androgenic impact of Testosterone (which has a score of 100 and 100 respectively). If you can get your hands on a bottle of this substance, I feel it would be best utilized as a part of a cutting cycle, stacked with some injectables (testosterone, etc…) but no other orals. It is just too dangerous. Negma (the French firm that introduced and subsequently abandoned Parabolan) never sought for MT to be approved as a commercially marketed substance since their first testing revealed it to be exceedingly harmful. Of course, methyltrienolone is a 19Nor molecule (as is Trenbolone)… As a result, it will affect your sexual drive and performance in a manner similar to Tren and Nandrolone, implying that temporary impotence and/or a lack of desire (also known as Tren-Dick or Deca Dick) is a distinct possibility. Another issue with MT is that it is a progestin that binds very effectively to the progesterone receptor (PgR). Progestins, as we know, increase the estrogenic effects of aromatizing medicines.
The compound methyltrienolone was discovered in 1965. As soon as it was discovered, it was recognized as a highly effective anabolic agent, substantially more effective than the commercially available anabolic agents at the time. Despite its great relative activity, however, methyltrienolone has had only a limited amount of application in human medicine. During the late 1960s and early 1970s, it was utilized clinically, most notably in the treatment of advanced breast cancer, and it is still in use today. In this case, the drug’s extremely potent anabolic/androgenic action aids in the countering of the local effects of endogenous estrogens, allowing it to be effective in slowing or even regressing tumor growth to a certain extent. Such an application, however, did not last long, since more realistic assessments of the drug’s toxicity quickly led to the drug’s discontinuation from use in human medicine.
The use of methyltrienolone in non-human research investigations, particularly in those relevant to the study of androgen receptor activation, had become commonplace by the mid-1970s. The agent is exceptionally well suited for this function. As a result of its high potency and resistance to serum-binding proteins, it serves as an ideal in-vitro receptor-binding benchmark against which other drugs can be measured. Because active methyltrienolone metabolites are so resistant to metabolism, they are unlikely to have a significant impact on the outcomes of most tests. Most steroids are easily metabolized by body tissues, which means that even incubation studies can be complicated by the question of whether it is the steroid itself or one of its undiscovered metabolites that are generating a particular impact. When it comes to methyltrienolone, this is far less of a concern. At this time, methyltrienolone is still only used for research purposes.
Negative side effects
MT does not aromatize, but you should be concerned about its possibility to induce negative effects by increasing the estrogenic concerns caused by other chemicals you may be taking. How dangerous is this stuff? It was never commercially commercialized for usage in humans, and it has been confined to Steroid-Purgatory, where it is solely utilized in research. I would put it on a par with taking really high amounts of halotestin or methyltestosterone. And I would definitely advise folks to keep dosages of this product extremely low, far lower than the suggested levels for the other two substances I just listed (500-750mcgs/day, for no more than 3-4 weeks). I had the good opportunity to discuss this product with the proprietor of an Underground Lab, and he had handed out numerous samples of this material to athletes he knew, all of whom maintained records and had regular bloodwork done. People who took 2mg/day experienced extremely increased liver enzymes and jaundice (yellowing of the eyes and skin). They all recovered, and after trial and error, it was discovered that a 500-750mcg dosage was (*relatively) safe and (*roughly) as effective as 150-225mgs of Trenbolone Acetate. Virilization (growth of male sexual features) is a potential adverse effect of MT for women, which is severe with this material, thus it is completely off-limits for women to use. If you decide to try it, you should take milk thistle (320mgs/day), ALA (500mgs per meal), and try some Pygeum Africanum (Permixon, the liposterolic extract of Serenoa)… all of this stuff will protect either your prostate or liver… in one study, it inhibited competitively the binding of Methyltrienolone to the cytosolic receptor of the rat prostate. You will still need to have a blood test done, avoid other orals (such as drinking or anything else that might stress your liver), and keep a tight eye on your health. This is certainly not a medicine for beginners, and it is most likely only effective for pre-contest bodybuilders.
Because methyltrienolone exhibits no estrogenic action in the same way as trenbolone does, the possibility of estrogenic adverse effects is not a worry with this chemical in and of itself. It is also resistant to the enzyme 5 alpha-reductase, although this is of little comfort to a user since methyltrienolone is already one of the most androgenic medicines in regular usage by steroid users, making it an even greater source of concern. As a result, androgenic side effects should be predicted by the majority of users who use this medication on a regular basis in cycles. Users have often reported symptoms such as prostate enlargement and greasy skin/acne. Additionally, the drug’s impact on the user’s hair should be similar to that of trenbolone. A large number of users have stated that trenbolone is one of, if not the most, severe compounds for causing hair loss. In the case of methyltrienolone, the same may be stated. When it comes to male pattern baldness, this substance may be best avoided by those who are genetically prone to it.
Given the strong androgenic character of methyltrienolone as well as the many adverse effects linked with this molecule, it should come as no surprise that women are not advised to take this substance. Female users are likely to experience the typical virilizing effects of the drug, such as depth of the voice, body/facial hair development, and enlargement of the clitoris, among other things. As seen in animal research, these side effects may manifest themselves even at very modest dosages. Attempting to inject methyltrienolone is not a task that should be undertaken by women.
It would seem that users of methyltrienolone would have nothing to worry about in terms of side effects such as gynecomastia, water retention, and the like because of the absence of estrogenic adverse effects linked with the substance. Methyltrienolone, like trenbolone, is a progestin, which means that it has the capacity to connect to receptors for the female sex hormone progesterone, just as trenbolone does. In addition, methyltrienolone, like other 19-nor substances, has been shown to elevate prolactin levels. Breast development and lactation may occur as a result of these responses as well as other side effects. Additionally, the medicine has the potential to increase any estrogenic adverse effects that may occur as a consequence of the usage of aromatizing therapies when the drug is being administered simultaneously. This is certainly something to consider when determining which auxiliary medications to employ in conjunction with methyltrienolone during a cycle that contains the substance. A number of medications, including bromocriptine, vitamin B6, and/or cabergoline, may be used to reduce the negative effects associated with high prolactin levels in a user’s system. Letrozole may also be used to reduce the amount of progesterone in the body.
Due to the fact that it is a progestin, methyltrienolone has a significant impact on the user’s natural testosterone production. In a manner similar to that of trenbolone and nandrolone, the anabolic steroids methyltrienolone and nandrolone may restrict the body’s natural testosterone production for a lengthy period of time. Users who seek to prevent sexual dysfunction, libido issues, or mental negative effects linked with a shortage of testosterone may consider using testosterone in combination with methyltrienolone, even during short cycles, according to the research. However, some animal studies have indicated that methyltrienolone may actually improve libido in certain situations, while others have discovered that the converse is true in other cases. As a preventative strategy, testosterone supplementation may be a wise course of action to take.
In accordance with the information provided previously in this profile, the business that developed methyltrienolone determined that it was too hepatotoxic for commercial human usage. As a 17 alpha alkylated steroid, it would be reasonable to expect that the medicine would place an extra burden on the liver of the individual who consumed it. Methyltrienolone, on the other hand, seems to be one of the most harmful steroids in terms of hepatotoxicity. As a result, if a user consumes methyltrienolone for a prolonged length of time, it is reasonable to suppose that his or her liver readings may become raised. In fact, if the user has any liver issues or if the dosages or durations of cycling the medication are outside of the accepted norms, liver damage might be a substantial concern. The use of other 17 alpha-alkylated steroids at the same time as methyltrienolone, or even at a time that is reasonably near to that of the medication, is thus deemed to be a danger that should be avoided at all costs.
What you should know about methyltrienolone
Methyltrienolone was previously a black market experimental steroid. It functions similarly to Trenbolone, with one exception. Methyltrienolone is C-17 alpha alkylated, making it orally active. Aside from that, this medicine has a high anabolic index and works hard to bind progesterone and glucocorticoid receptors.
Even though it demonstrates how robust the binding process is in Methyltrienolone, its affinity for the PR is more than 40 times more than that of testosterone. Aside from that, MTren has a strong androgenic impact, lowering HDL levels. When it comes to its androgenic and anabolic ratio, the anabolic benefits it delivers work 120 times harder than testosterone, while the androgenic effects work 60 times harder. When taken orally, this is comparable to methyltestosterone.
What is the ideal MTren cycle duration?
When it comes to MTren cycle duration, four weeks is considered the normal amount that users generally restrict themselves to. Male users must take 400mg-800mg, however, ladies do not have to take MTren. Females should avoid using the medicine due to its virilizing effects, which include clitoris enlargement, body or facial hair development, and voice deepening.
Methyltrienolone is a progestin
Methylenetrienolone is classified as a progestin. Progestins are synthetic progestogens that mimic the actions of progesterone. Methyltrienolone is classified as a progestin due to the substantial influence it has on a user’s natural testosterone production. MTren lowers natural testosterone production over a longer length of time, enabling the user to take testosterone as a companion with this medicine. Many people use MTren with testosterone to treat libido issues, sexual dysfunction, and mental negative effects that are obviously related to testosterone deficiency.
Is Methyltrienolone a hepatotoxic substance?
Many people have stated that using Methyltrienolone may harm your liver. Because using this steroid might cause liver problems, persons who desire to use it and develop liver abnormalities are no longer permitted to do so. Even having other alpha-alkylated steroids is not suggested due to the additional hazards they may pose.
How to buy steroids online safely
It is always urged to use extreme caution while purchasing steroids such as Methyltrienolone online. There are just a few places that sell these items at a low cost, while others charge a high price. Steroids are not very cost-effective. In truth, producers offer them at a price that is appropriate for their components and effects.
Before you purchase MTren online, you need first to understand what the product is. It is good to study it, specifically its advantages and disadvantages. You must be extremely careful not just with the drug’s information, but also with the manufacturer’s. It is also vital to confirm the drug’s validity. You do not want to be a victim of fraudsters, therefore be cautious with your measurement.
Methyltrienolone is fundamentally the same molecule as trenbolone, but it has been subjected to 17 alpha alkylation in order to retain its activity after oral administration. To put it another way, methyltrienolone has all of the benefits that trenbolone has, with the additional benefit of being orally active. However, as will be illustrated in the next section, that additional advantage comes at a high cost in terms of hepatotoxicity.
Additionally, similar to trenbolone, methyltrienolone has an extraordinarily great binding affinity for the androgen receptor, which is even stronger than that of testosterone. Of course, this confirms the claim that trenbolone is particularly anabolic, since attaching to the androgen receptor allows a substance to activate the anabolic pathways that are reliant on the androgen receptor, which is one of the numerous ways in which anabolic steroids help in muscle building. Androgen receptors may be found in fat tissue as well. When they are triggered by a chemical such as methyltrienolone binding to them, this may result in a greater than typical lipolytic effect. Not only can this medication aid in the development of muscle, but it also has the potential to aid in the reduction of fat.
Another notable aspect of methyltrienolone is its ability to inhibit catabolic activity in the body. Metabolic hormones like glucocorticoids and methyltrienolone attach to receptors on the surface of the body that interact with glucocorticoids. Since a result of its ability to block cortisol and several other catabolic hormones in the body, methyltrienolone is particularly beneficial for people aiming to lose body fat, as the substance will aid to prevent muscle loss while following an eating plan that is deficient in calories.
Cycle and dosage
A French pharmaceutical firm initially created methyltrienolone, but it was never commercially manufactured owing to the severe hepatotoxic effects of the compound on the liver. This should provide an indication of just how severe this medication is. As a result, it is critical that users exercise care while administering this medication and that they limit the duration of their cycles to a short length of time. Additionally, additional steroids that are very hepatotoxic, such as 17 alpha alkylated oral steroids, would be prohibited.
When it comes to cycle duration, four weeks is the normal time that most users adhere to, if not less often. Any prolongation of this period would entail the administration of ongoing blood tests by a physician, which is a good idea regardless of how long a user plans to take this medication. As with any drug, individual responses to it and a user’s liver function would be important factors in how well a user would tolerate methyltrienolone and, consequently, how well the drug would be tolerated and run.
As for dosage, since the little study has been done on methyltrienolone since its introduction, we must rely on anecdotal evidence to estimate the precise amount of the molecule that should be administered in order to reap the advantages while also minimizing the unwanted effects. Doses ranging from 400 to 800 micrograms per kilogram of body weight for male users are pretty common for most. As will be explained more in the section below, it is not suggested that females give this medication. Of course, as with all medications, considerably larger dosages have been tested than those used here. A significant increase in the number of reports of undesirable side effects, particularly transient liver problems such as jaundice, has resulted as a result of this. In order to avoid adverse effects, it is suggested that users use extreme caution while administering this substance at low doses and when increasing their doses later on.
It has been demonstrated in studies that taking an oral anabolic steroid with food can reduce its bioavailability. That is because steroid hormones are fat-soluble, which means that some of the medication can dissolve with undigested dietary fat, which reduces the amount of drug absorbed from the digestive tract. Methyltrienolone should be consumed on an empty stomach in order to maximize its absorption.
It is no longer recommended for use in clinical medicine due to an unacceptable amount of hepatotoxicity associated with it.
For the same reason, this substance is generally not recommended for use in the enhancement of one’s physical appearance or performance. It is imperative that those who are adamant about using it do so with full awareness of the extent of its liver harm. It is recommended that at the very least, routine blood tests be performed to check that the agent is not causing harm. In addition, the period of drug use should be kept to a bare minimum, preferably no more than 4 weeks. Meltrienolone has extraordinarily high relative potency, necessitating doses of as little as.5 milligrams per day to get maximum effect. This medication’s effective and tolerated dose range is typically believed to be between.5 and 2mg per day. Dosages of 20-30 mg per day, similar to those used by Dianabol, are utterly unfathomable and should never be attempted. Once again, this is a highly hazardous steroid, and all sound advice would tell you to stay away from it. Any of the numerous commercially available anabolic steroids would be far safer alternatives.
It is no longer recommended for use in clinical medicine due to an unacceptable amount of hepatotoxicity associated with it.
As a result of its exceptionally high toxicity and proclivity to cause virilizing side effects, this drug is not suggested for use by women for the goal of boosting their physique or performance.
What happens to this medication after it enters your body?
Here’s how it works:
Once digested by stomach acids, methyltrienolone attaches to androgen receptors, causing a significant increase in androgen production. In essence, androgens are male sex hormones that are responsible for the production of anabolic effects in humans. It is important to note that androgen receptors are the principal mechanism through which these hormones generate their anabolic effects. They stimulate a number of genes, which results in an increase in muscle mass and strength over time. One of the many androgens, testosterone is the primary hormone responsible for the growth and repair of your bodily tissues. Androgen receptors are responsible for ensuring that the body responds effectively to the hormone that has been released. As a result of this interaction, testosterone is transported to the skeletal muscle cells, where it performs its function. Methyltrienolone, with its strong affinity to androgen receptors, aids in the activation of testosterone’s actions, hence facilitating the development of lean muscle mass and increased strength.