Weight loss material AICAR Acadesine/steroidmisty@ycphar.com

Product Name:AICAR,Acadesine
Chemical Name:5-Aminoimidazole-4-carboxamide ribonucleotide
CAS NO.:2627-69-2
Molecular Formula:C9H14N4O5
Molecular Weight:258.231
Purity:99%
Appearance:White Powder
Grade:Pharmaceutical Grade

Fat Loss

AICAR is a peptide, which is an intermediate within the generation of inosine monophosphate and directly related to metabolic regulation. The most important mechanism that AICAR is known for is its ability to block enzymes both in intracellular and extracellular levels, which, in turn, allows for an accelerated stimulation of glucose uptake and increase protein kinases in skeletal muscle tissue. These two functions allow for more energy conversion, which helps burn fat and also sustain output in activity. This is what scientists and athletes/bodybuilders are interested in.

AMP-activated Protein Kinase

AICAR’s principal mechanism of action is activation of AMPK (AMP-activated protein kinase.) Activating AMPK, therefore, causes the same cellular machinery (so to speak) to be turned on as if the cell were energy deprived, for example from intensive exercise, or from low caloric intake.

AICAR, at sufficient and quite substantial concentration, is effective at activating AMPK and inducing a cellular state as if exercise had been performed, or energy stores were low and fat therefore needed to be burned.

AICAR uses metabolic pathways to block certain enzymes, which allows for AMP-activated protein kinase. This can be explained to the layperson like this: once you take a substantial amount of AICAR, it tricks your body at a cellular level in to thinking that exercise has just been preformed. Since the body thinks it has just done a considerable amount of exercise, the energy cycle at the cellular level starts converting fuel sources, like fatty acids, to output the energy that was thought to have been spent during exercise. This can have a direct effect on the level of endurance activity and the sustainability of that activity. Insulin sensitivity is also noted to be one action that AICAR produces, as the body will think it just went through a series of exercises. Interestingly, in animal studies with obese mice, AICAR showed all of the peptides benefits for obese diet induced mice, yet the healthy lean mice did not reap any of the benefits of insulin sensitivity or increase in glucose uptake. That being said, the application in bodybuilding does not seem very suitable, as these mechanisms are targeted for the out-of-shape and over-weight.

Protect against ischemic Injury

Interestingly, AICAR has been shown to protect against ischemic injury. This type of injury is directly related to the restriction of blood to tissues, which can cause insufficient amounts of oxygen and glucose needed to keep the tissue alive. This can lead to thrombosis, embolisms, and vasoconstriction. AICAR can be used as a stabilizing peptide for ischemic episodes, and it can allow for proper blood flow to the myocardium (heart). This function is very interesting, as AICAR could be fundamentally used to treat the heart muscle in the aftermath of a heart attack. This might reduce the possibility for ischemic injuries. Abnormal growths of heart tissues and heart valve function have also been altered in animal studies that used the peptide AICAR, which is a downside.

Weight loss 2,4-Dinitrophenol/steroidmisty@ycphar.com

Product Name:2,4-Dinitrophenol Sodium Salt
Alias:Sodium 2,4-dinitrophenate
CAS NO.:1011-73-0
Molecular Formula:C6H3N2NaO5
Molecular Weight:206.09
Purity:99%
Appearance:Orange Yellow Powder
Grade:Pharmaceutical Grade

DNP is an extremely powerful and beyond controversial fat burning drug. There is no compound on earth that can burn fat at the rate of DNP; however, to say it is beyond dangerous is almost an understatement. DNP is so dangerous it can in fact kill you. No one can deny the fat loss power held by this compound is truly tremendous, but when we consider the risk there are very few if any we can recommend it too.

Effects of DNP

The effects of DNP are very simple and very straightforward, tremendous fat loss and loss of total bodyweight. So powerful, the effects of DNP can result in a full pound of body fat loss per day. Note we said a full pound of body fat, not merely weight but actual pure body fat. That is truly amazing and could easily result in twenty plus pounds of fat loss in only a few weeks, not to mention any other weight lost, i.e. water weight.

That’s it, pure fat loss, rapid and tremendous fat loss represents the full effects of DNP. The compound carries no additional traits that could be potentially desired by any human being. While sometimes labeled as a performance enhancing drug DNP carries no anabolic properties. The compound will not help the individual build muscle mass or enhance strength. The individual will not see his athletic performance enhanced; in fact, many would see it diminished as DNP can be extremely draining on energy levels. Further, due to the tremendous increase in body temperature, when we look at the side effects of DNP we will find extreme activity must be avoided when using the compound.

When looking at the effects of DNP in a performance setting, many are often curious about its fat loss power compared to other more commonly used medications. The two most commonly used fat loss aids in performance enhancement circles are undoubtedly Clenbuterol and Cytomel (T3), and both are highly effective. However, while we cannot recommend DNP and while both Clen and T3 are far safer, we cannot deny the truth. DNP is far more powerful and will lead to greater and more dramatic fat loss than both Clenbuterol and Cytomel combined. This is simply the truth; however, both Clenbuterol and Cytomel can easily be used without severe or even fatal consequences, but we cannot say the same for DNP. Absolutely, DNP can be used without it leading to your death, there are those that get away with it, but the overall risk is so great you are truly playing with fire. At Steroid.com our job is to simply give you the truth. When explaining and covering various hormones and compounds, our job is to tell you exactly what the hormones and compounds in question can do. It is not our job to insight fear, or to embellish risks that may be associated with a compound in question. Our job is to take a neutral stance and simply explain what a compound can do, the good and the bad and nothing more. But when it comes to DNP it truly is pure poison and that is not an embellished statement. Regardless, some of you will still try it and while some of you will have success others will face horrific consequences and that’s the truth.

Side Effects of DNP

There are not too many side effects of DNP use, but what does exist is tremendously damaging. Of the side effects of DNP the most concerning is death. We actually mean your heart stopping and you living no more. There have been numerous deaths reported due to DNP use over the years. Although the compound is no longer legitimately obtainable on the pharmaceutical market, death will still be a possible side effect for those who are able to find it.

Beyond death, the most common side effects of DNP use include dramatic insomnia, nausea and extreme sweating. When we refer to extreme sweating, a more accurate way to describe it would be sweating profusely. Many who have used DNP have reported ruining their mattress during periods of use due to the sweating being so intense. DNP is also well-known for causing cataracts, which in many cases ultimately leads to the individual going blind.

DNP can also have a strong, negative impact on white blood cell count by reducing the total count severely. This can have a disastrous effect on the individual’s immune system. You will be far more susceptible to viruses and infections when using DNP. It is also very common for those who use DNP to fall into a coma, which can very easily lead to an untimely death. So powerful is the compound and so great is the risk of death, reports have indicated that death can occur with only a few days of use. Talk about a risk and one that is not worth taking.

Anabolic steroids Lorcaserin hydrochloride/steroidmisty@ycphar.com

Product Name: Lorcaserin HCl
CAS: 846589-98-8
MF: C11H14ClNClH
MW: 232.1525
Appearance:White Powder
Grade:Pharmaceutical Grade

Lorcaserin, currently marketed under the trade name Belviq and previously Lorqess during development,is a weight-loss drug developed by Arena Pharmaceuticals. It has serotonergic properties and acts as an anorectic.

Lorcaserin is used long term for weight loss in those who are obese.BELVIQ is an FDA-approved prescription weight-loss medication that, when used with diet and exercise, can help some overweight adults with a weight-related medical problem, or obese adults, lose weight and keep it off.

Lorcaserin VS Orlistat

Lorcaserin is a selective 5-HT2C receptor agonist,and in vitro testing of the drug showed reasonable selectivity for 5-HT2C over other related targets. 5-HT2C receptors are located almost exclusively in the brain. The activation of 5-HT2C receptors in the hypothalamus is supposed to activate proopiomelanocortin (POMC) production and consequently promote weight loss through satiety.The safety and effectiveness was tested in the 3 clinical trials which nearly 8000 overweight or obese participants were involved.

Orlistat works by inhibiting gastric and pancreatic lipases, the enzymes that break down triglycerides in the intestine. When lipase activity is blocked, triglycerides from the diet are not hydrolyzed into absorbable free fatty acids, and instead are excreted unchanged. Only trace amounts of orlistat are absorbed systemically; the primary effect is local lipase inhibition within the GI tract after an oral dose. The primary route of elimination is through the feces. But for a part of stubborn obesity who get good appetite, the treatment effect is not ideal.

Anabolic weight loss steroids Dextromethorphan Hydrobromide/steroidmisty@ycphar.com

Product Name:Dextromethorphan Hydrobromide 
Alias: Romilar,dextromethorphan,Demorphine,Dormetan 
CAS No.: 125-69-9 
EINECS No.: 204-750-1 
MF: C18H26BrNO 
MW: 352.31 
Purity: 98.0% 
Appearance: White or kind of white crystalline powder
Grade:Pharmaceutical Grade

Dextromethorphan (DXM or DM) is an antitussive (cough suppressant) drug.  Dextromethorphan has also found other uses in medicine, ranging from pain relief to psychological applications. It is sold in syrup, tablet, spray, and lozenge forms. In its pure form, dextromethorphan occurs as a white powder.

DXM is also used recreationally. When exceeding label-specified maximum dosages, dextromethorphan acts as a dissociative hallucinogen. Its mechanism of action is via multiple effects, including actions as a nonselective serotonin reuptake inhibitor and a sigma-1 receptor agonist.DXM and its major metabolite, dextrorphan, also acts as an NMDA receptor antagonist at high doses, which produces effects similar to, yet distinct from, the dissociative states created by other dissociative anaesthetics such as ketamine and phencyclidine. As well, the metabolite 3-methoxymorphinan of dextrorphan (thus a second-level metabolite of DXM) produces local anesthetic effects in rats with potency above dextrorphan, but below that of DXM.

DXM Effect

DXM has dissociative effects, somewhat similar to ketamine and PCP. The main effects are those of dissociation (separation of mind and body), which include:

Double vision and no perception of depth (eyes are not able to focus)
Altered kinesthetic sense (distorted perception of gravity and movements)
Overall reduction of external stimuli (loosens the connection between mind and body, can lead to out-of-body experiences)
Total loss of reality awareness (dissociative anaesthesia - at high doses)
Euphoria
Emotion amplification
Hallucinations (closed-eye visuals, vision trails and increased awareness of color, flanging of sound)
Music appreciation

Anabolic weight loss steroid Theobromine/steroidmisty@ycphar.com

Product Name:Theobromine
Alias:Diurobromine Theobromine,Teobromin,Theominal, Theoxalvose,Riddovydrin
CAS: 83-67-0
MF: C7H8N4O2
MW: 180.16
EINECS: 201-494-2
Assay: 99%
Appearance: White crystal powder

Theobromine, formerly known as xantheose, is a bitter alkaloid of the cacao plant, with the chemical formula C7H8N4O2. It is classified as a xanthine alkaloid, which also includes the similar compounds theophylline. The compounds differ in their degree of methylation.

Health Benefits of Theobromine

Theobromine has a similar effect than caffeine, but about 10 times weaker. Theobromine has diuretic, stimulant and relaxing effects. Theobromine can lower the blood pressure because it can to dilate blood vessels.
Theobromine has stimulant properties, similar to caffeine. Unlike caffeine theobromine does not affect the central nervous system. 
Theobromine can also relax bronchi muscles in the lungs. Theobromine can be used as cough medicine. Studies indicate that theobromine acts on the vagus nerve, which runs from the lungs to the brain. 

Weight Loss

Theobromine is a mild stimulant and diuretic. Both of these properties can aid weight loss by giving you a little energy boost for physical activity and helping you shed water weight. Theobromine can also help suppress your appetite.Theobromine can be said to promote weight loss in a variety of different ways including vasodilatation, diuresis and the ability to increase energy although most of these seem to be indirect.

Use

In modern medicine, theobromine is used as a vasodilator (a blood vessel widener), a diuretic (urination aid), and heart stimulant. Theobromine increases urine production. Because of this diuretic effect, and its ability to dilate blood vessels, theobromine has been used to treat high blood pressure.

Anabolic weight loss steroid Rimonabant/steroidmisty@ycphar.com

Product Name:Rimonabant
Alias:Acomplia,Zimulti,Rimonabdomining Exercisesish
CAS NO:168273-06-1 
Molecular Formula:C22H21Cl3N4O
Molecular Weight:463.79
Appearance:White to off-white crystalline powder
Purity:99.5%
Grade:Pharmaceutical Grade

Weight Loss

Rimonabant (trade name Acomplia) is an anorectic antiobesity drug that has been withdrawn from the market due to potentially serious side effects.Rimonabant is an inverse agonist for the cannabinoid receptor CB1.It has also been shown to be a μ-opioid receptor antagonist (possibly the contributing factor in its reported dysphoric qualities).Its main effect is reduction in appetite.Rimonabant works by blocking the cannabinoid receptors in the brain. This is designed to lower your food cravings in between meals and prevent you from munching on snacks when your body doesn't truly need food. The recommended dosage is only a single pill each day before breakfast.

The Rimonabant is a very great  weight loss powders in nowadays  markets ,and its purity is very high ,the contents is for 99% ;especially for smoker and is also for patients with cardiovascular diseases.

Application

1)Obesity,weight loss
2)Smoking cessation
3)Addiction behaviors
4)Short-term memory
5)Blockage of cannabis effects

Anabolic weight loss steroids L-Carnitine/steroidmisty@ycphar.com

Product Name:L-carnitine,Vitamin BT,L-ca greatrnitine,L-ctheirrnitine
CAS NO.:541-15-1
EINECS:208-768-0
Molecular Formula:C7H15NO3
Molecular Weight:161.20
Melting Point:200℃
Appearance:white crystal or transparent powder

L-Carnitine is a natural, vitamin-like nutrient wich plays an important role inhuman metabolism. It is essential in the utilization of fatty acids and in transporting metabolic energy.

Carnitine (carnitine) is an essential, non-toxic, natural nutrient that helps burn fat for fuel. Because deficiencies have been linked to a profound impairment of muscle function, there has been great interest in studying carnitine supplementation. Over the past decade, my research, as well as countless others, has shed light on carnitine’s role in metabolism, performance and overall health.

Carnitine burns body fat 

Carnitine has an essential role in transporting fat into mitochondria (the furnace of the cell). Therefore, carnitine has been marketed as a fat burning supplement.Carnitine is a substance that helps the body turn fat into energy. Your body makes it in the liver and kidneys and stores it in the skeletal muscles, heart, brain, and sperm.

Usually, your body can make all the carnitine it needs. Some people, however, may not have enough carnitine because their bodies cannot make enough or can’t transport it into tissues so it can be used. Some other conditions, such as angina or intermittent claudication, can also cause low levels of carnitine in the body, as can some medications.

Carnitine has been proposed as a treatment for many conditions because it acts as an antioxidant. Antioxidants fight harmful particles in the body known as free radicals, which damage cells and tamper with DNA. Antioxidants can neutralize free radicals and may reduce or help prevent some of the damage they cause.

Anabolic weight loss steroids 1,3-dimethylpentylamine hydrochloride/steroidmisty@ycphar.com

Product Name:Methylhexanamine,DMAA
Alias:dimethylamylamine,methylhexamine
CAS Registry Number:13803-74-2
Molecular Formula:C7H18ClN
Molecular Weight:151.68
Appearance:White Crystalline powder
Grade:Pharmaceutical Grade

Methylhexanamine is synthesized by reacting 4-methylhexanone-2 with hydroxylamine, which converts the 4-methylhexanone-2 to 4-methylhexanone-2 oxime, which is reduced with hydrogen by means of a catalyst; the resulting methylhexanamine can be purified by distillation.

Fat Loss

A large number of supplements focusing on fat loss and workout energy (thermogenic or general-purpose stimulants) now use the ingredient in concert with other substances such as caffeine, a combination similar to the combination of ephedrine and caffeine.

Methylhexanamine is an indirect sympathomimetic drug that constricts blood vessels and thus has effects on the heart, lungs, and reproductive organs it also causes bronchodilation, inhibits peristalsis in the intestines, and has diuretic effects.Most studies have been done on pharmacological effects when the drug is inhaled; our understanding of what methylhexanamine does when taken orally are mostly based on extrapolating from the activities of similar compounds.Today, dimethylamylamine is sold as a dietary supplement used for attention deficit-hyperactive disorder (ADHD), weight loss, improving athletic performance, and body building.

Athletes and bodybuilders are constantly persuing lean body mass.When it comes to sports performance and building,some turn to dietary and sports improving supplements to boost their athletic performance or lose body fat. One such supplement ingredient called methylhexamamine or DMAA is advertised for this objective and is currently the topic of some controversy.

How Does DMAA Work?

DMAA has stimulant results significantly like caffeine. Individuals who take it experience more energized and have better mental focus without any the jitteriness that many people experience when they drink an excessive amount of caffeine. At exactly the same time, DMAA causes constriction of blood vessels and dilation of bronchioles in the lungs.It’s also an appetite suppressant and may cause weight loss in some people.

Using and Dosage

A typical starting dose of 1,3-DMAA is in the 10-20mg range and eventually reaching up to 40-60mg a day, there is no actual evidence to support this dosage range but it seems to be the standard dosages range for supplemental 1,3-DMAA on the market.

Anabolic weight loss steroid Furazabol/steroidmisty@ycphar.com

Product Name: Furazabol
Alias: Miotolon
CAS No.: 1239-29-8
EINECS: 214-983-0
Molecular formula: C20H30N2O2
Molecular weight: 330.46
Assay: 98%
Grade:Pharmaceutical Grade
Appearance: White crystalline powder

Bodybuilding Benefits

Furazabol (Miotolan) is a 17-alpha-alkylated oral steroid that is derived from dihydrotestosterone (DHT),it is a derivative of the anabolic steroid stanozolol. It differs from stanozolol by having a furazan ring system in place of  the pyrazole. It has a c-17alpha methyl group, which allows it to be taken orally and causes hepatotoxicity in some individuals.Furazabol does not aromatize and also has very minimal bloat, that is why there is little to no water retention when administering the drug, and muscle begins to appear much denser and harder,therefore it should produce a lean and vascular appearance. 

Interestingly, it also has no 3-keto group,  which is needed for androgenic binding . This obviously hinders the androgenic activity of the compound and thus limits its muscle and strength building abilities. Due to its androgenic effects and lack of estrogenic activity, bodybuilders with relatively low body fat should notice a muscle hardening effect when using adequate dosages.Its moderately potent androgenic activity, give it a fairly low risk for gyno or negative effects on the libido. These are traits shared by Stanozolol. It is for this reason that Furazabol is most commonly compared to Stanozolol in both their structures and effects.

Noticeable gains in lean muscle mass and strength are likely not going to be achieved unless doses of at least 200mg/day are used. Big increases in weight are not likely to happen with this steroid either, so increased blood pressure and painful back pumps should not be a problem. If used for the specific purpose of enhancing the appearance of the user muscle, Furazabol can be quite beneficial when used in conjunction with other anabolic compounds. 

Risks/Side Effects of Furazabol

Furazabol can not aromatize and therefore estrogenic side effects are not a concern with this compound. As well, the drug is relatively mild in terms of expected androgenic side effects and therefore these should not be a source of concern for most users. This is also a reason why Furazabol is a relatively safe choice for women. 

The only real cause of concern for most users would be that the compound is derived from dihydrotestosterone as it relates to (1,4). This of course will indicate that side effects associated with dihydrotestosterone could become apparent with use of the drug. Hair loss, acne and prostate enlargement are all possible side effects that could be encountered when administering the compound. 

Finasteride will usually help in preventing or minimizing the effects of dihydrotestosterone, but it will not help with this as a result of furazabol. This is due to the fact that as stated the drug is derived from dihydrotestosterone and so its androgenic activity will not be increased via interaction with the 5 alpha reductase enzyme. However these related side effects should be tolerable if dosages and cycle length are kept within reasonable limits. 

As noted earlier, since the compound is 17-alpha-alkylated liver values will likely be raised when administering it. For this reason, and the fact that permanent liver damage is possible, it is recommended that a user limit their use of the drug to about 4-8 weeks. This moderate length of use should not result in any serious complications in terms of liver health. 

Use/Dosing of Furazabol

In terms of dosing, for inexperienced males users, doses in the range of 30-90 milligrams per day should be sufficient to promote very noticeable gains. Due to the short active life of the compound, multiple doses a day should be administered. Three to four would likely be the minimum needed to provide the users with stable blood concentrations of the drug. 

In terms of the appropriate dosage for use by women, 5 to 20 milligrams per day should be adequate to experience gains in muscle mass and density. As always however, doses larger than those recommended here have been experimented with by both males and females. Of course with these increasing doses come greater risks and likelihood undesirable side effects will be experienced. 

While there have been some studies conducted that have indicated that Furazabol has little effect on endogenous testosterone production, for the most part these studies used relatively small doses , much smaller than would be needed to experience any type of muscle building effect. For this reason, along with the fact that it is unlikely that any male users would administer Furazabol without running any other type of anabolic steroid(s) in conjunction with it, the regular post-cycle recovery protocol should be followed. 

Anabolic weight loss steroid Orlistat/steroidmisty@ycphar.com

Product name: Orlistat
Brand Name:Myalli,Xenical,Alli
CAS: 96829-58-2
Molecular Formula: C29H53NO5
Molecualr Weight: 495.73
Assay: 99%
Grade:Pharmaceutical Grade
Appearance:White Crystalline Powder

Fat Loss Mechanism

Orlistat is a drug that promotes loss of weight by preventing the digestion and absorption of fat in food. In the intestine, an enzyme called lipase (produced primarily by the pancreas) breaks apart fat in food so that it can be absorbed into the body. Orlistat blocks the action of lipase and thereby prevents the breakup and absorption of fat. Orlistat blocks absorption of about 25% of the fat in a meal. The unabsorbed fat is excreted in the stool. 

This medication is used along with a doctor-approved reduced-calorie diet, exercise, and behavior modification program to help significantly overweight (obese) persons lose weight. Taking orlistat can also help prevent you from regaining the weight you have lost. Losing weight and keeping it off can reduce the many health risks that obesity causes, including heart disease, diabetes, high blood pressure, some forms of cancer, certain breathing problems, and a shorter life span.

Dietary fats need to be broken down into smaller pieces before the body can absorb them. Orlistat works by blocking the enzyme that breaks down fats in your diet. This undigested fat then passes out of your body in your bowel movement. Orlistat does not block the absorption of calories from sugar and other non-fat foods, so you still need to restrict your total intake of calories.

Fat Loss Effect

Orlistat is used for the treatment of obesity. The amount of weight loss achieved with orlistat varies. In one-year clinical trials, between 35.5% and 54.8% of subjects achieved a 5% or greater decrease in body mass, although not all of this mass was necessarily fat. Between 16.4% and 24.8% achieved at least a 10% decrease in body fat.After orlistat was stopped, a significant number of subjects regained weight-up to 35% of the weight they had lost.

The incidence of type 2 diabetes in an obese population over four years is decreased with orlistat (6.2%) compared to placebo (9.0%).Long-term use of orlistat also leads to a modest reduction in blood pressure (mean reductions of 2.5 and 1.9 mmHg in systolic and diastolic blood pressure respectively).

Orlistat Dosage

Orlistat is usually taken 3 times a day during every meal containing fat. The average dosage is a 120mg per day. Due to the fact that Xenical may decrease the absorption of vitamins and it is useful to take a multivitamin once a day at bedtime. While taking this drug bodybuilders and athletes should follow their diet, medication, and exercise routines very closely.

Anabolic weight loss steroid Liothyronine Sodium T3/steroidmisty@ycphar.com

6893-02-3

Product Name:T3,Cytomel
Alias: Triiodothyronine
CAS NO: 55-06-1
Einecs No: 200-223-5
MF: C15H11I3NNaO4
MW: 672.96
Purity: 98.0%
Appearance: white or light yellow powder

Fat Loss

Liothyronine is the most potent form of thyroid hormone. Chemically, it is nearly identical to triiodothyronine (T3). As such, it acts on the body to increase the basal metabolic rate, affect protein synthesis and increase the body's sensitivity to catecholamines (such as adrenaline) by permissiveness. The thyroid hormones are essential to proper development and differentiation of all cells of the human body. These hormones also regulate protein, fat, and carbohydrate metabolism, affecting how human cells use energetic compounds.

T3 is a regulator of the oxidative metabolism of energy. When you take liothyronine sodium it will increase the uptake of nutrients into the mitochondria, which raises activity in the oxidative metabolic pathway. This causes everything to work harder within the organism and makes the body demand more fuel.

T3 in the body is responsible for regulating the uptake of various nutrients into cells and into the mitochondria of those cells in order to effectively become utilized for the production and consumption of energy.The mitochondria of every single cell in the body utilizes carbohydrates (primarily), fat, and even protein for the production of an energy source known as ATP (Adenosine Triphosphate). Through the intake of more T3, this production of ATP will increase, leading to an increased rate of energy consumption in the form of fats,carbohydrates, and protein. Hence, this is why the consumption of too much T3  without the use of anabolic steroids can result in muscle loss.

Bodybuilding

The increase of ATP and metabolic activity leads the body to burn fat. This is why bodybuilders use T3 as a part of their anabolic steroid stacks. Furthermore, T3 is popular among bodybuilders because it can help burn those stubborn 1 to 2% of body fat that won’t come off through just diet and cardio.

Another interesting property of Cytomel is that it can enhance growth hormone (GH) production. 

Dosages of T3

In the first approach, the goal is to achieve an ongoing edge in fat loss or to help maintain a near-personally-ideal body composition. In this approach, T3 dosing is very low, preferably 12.5 mcg/day but in some cases as much as 25 mcg/day. At the lower end of this range, typically thyroid testing will show no detectable suppression even with prolonged use. At the higher end, moderate suppression is sometimes seen, but results are superior to when T3 is not taken, and the suppression reverses rapidly upon discontinuing T3 use.

In the second approach, the goal is to achieve a quite substantial increase in rate of fat loss, at the known cost of inducing thyroid suppression. Most preferably the dosage is about 50 mcg/day, but in some instances can be as high as 75 mcg/day. Such use is preferably not ongoing, but only for a limited period of time such as 8-12 weeks, though there’s no exact requirement for timeframe.

Bodybuilding Raw Powder Metribolone/steroidmisty@ycphar.com

Product name: Metribolone
Alias: Methyltrenbolone,Methyltrienolone
CAS register number: 965-93-5
Molecular formula: C19H24O2
Molecular weight: 284.39
Assay: 98%
Appearance: yellow or light yellow crystalline powder
Grade: Pharmaceutical Grade
Usage: a steroid to help burn fat and maintain muscle tissue. 

Metribolone, also known as methyltrienolone is a potent, non-aromatizable androgen which has also been used as a photoaffinity label for the androgen receptor. It is the 17-methylated derivative of trenbolone, and is a similarly potent anabolic steroid, but with high hepatotoxicity. Methyltrienolone binds strongly to the androgen receptor (AR) and is a more potent agonist (activator) of the androgen receptor than is DHT.

Metribolone binds onto the AR receptor so strongly that it is pretty much the benchmark for that quality.Androgen Receptors are found in both fat cells as well as muscle cells; they act on the AR in muscle cells to promote growth, and in the fat cells to affect fat burning.The stronger the androgen binds to the A.R, the higher the lipolytic fat burning effect on adipose fattissue. MT is basically a 17aa (oral) version of (injectable) Trenbolone. AR binding and AR stimulation is not the only mechanism which stimulates anabolism.

Metribolone is an anabolic steroid that is available for oral administration as tablets and is available also as injection.
Generally, most of the users tend to take metribolone for a shorter period of time at the room temperature below 30 degrees C.

Metribolone is steroid hormone which can increase muscular endurance and explosive power,it is the most powerful anabolic steroids ever producedIt can also Treatment of advanced and recurrent breast cancer and ovarian cancer and other diseases.

Side Effects

It is also one of the most hepatotoxic androgens ever produced. even though it is very toxic to liver and kidneys.

Comparisons to oral trenbolone

A lot of people on forums will compare metribolone to oral trenbolone, and online steroid ‘gurus’ will claim that metribolone is the “most powerful steroid ever.”  Are they right?

If you take a look at the structure, the first difference is that oral trenbolone is not 17-aa, while metribolone is methylated in a big way.  Moreover, on paper metribolone may appear to be hundreds of times more powerful than straight testosterone, but things on paper can be misleading; in fact, those who used metribolone say that it is milder than oral trenbolone, yet it is much more toxic because of the liver strain that occurs.

Although they are very similar in structure, methyltrienolone is very different in effect from trenbolone. It has an anabolic to androgenic ratio of 12000/6000 in comparison to methyl-testosterone, making it possibly the most potent steroid in existence. Methyltrienolone may also be the strongest androgen receptor binder of all steroids. Methyltrienolone required very small doses to see big gains in size and strength. Methyltrienolone does not convert to estrogen, but it does have progestational activity which may increase the effects of estrogen. This can be considered a “dry” compound that will not cause much if anything for subcutaneous (under the skin) water retention.