Anabolic steroids Calcium Pyruvate/steroidmisty@ycphar.com

Product Name:Calcium pyruvate
Synonym: Pyruvic acid Calcium salt; Pyruvic acid calcium 
CAS: 52009-14-0 
MF: C6H6CaO6
MW: 214.19 
EINECS: 257-599-9 
Appearance: White to light yellow powder 
Purity: 99%
Grade:Pharmaceutical Grade

Fat Loss

Calcium pyruvate can enhance exercise endurance, increase cell energy, prevent or reduce due to too much caused by the consumption of fat and increase in body weight, heart, muscle inhibition efficiency, reduce the high fat fed cholesterol. 

Pyruvate is a 3-carbon energy intermediate produced in cells from glucose, en route to creating ATP (the main energy currency of working cells). Pyruvate supplementation has been proposed to enhance work output and weight loss by providing more efficient energy that bypasses the ability of the body to store glucose as body fat.

Many claim that calcium pyruvate can help with weight and/or fat loss. In theory, since it is the raw material for cellular respiration, supplementing with calcium pyruvate should increase the amount of energy burned, therefore allowing for more fat burning. The question is whether this is actually the case. A study done by Dr. Ronald Stanko at the University of Pittsburgh concluded that calcium pyruvate does have this fat burning effect. Obese women were put on a 1,000-calorie diet for 21 days during this study. The group receiving calcium pyruvate experienced 48 percent higher fat loss, amounting to 3.2 extra pounds. However, very large doses of 30 grams per day were used to elicit this result. The common recommendation of 5 grams per day may not be enough to produce similar results. The expense of high dosage supplementation with calcium pyruvate may be too expensive for some. Diet-and-Health.net discounts the research, claiming that there is still no solid evidence for weight loss benefits.

Application

1. Calcium pyruvate as dietary supplements, has accelerated fat consumption, reduce weight, enhance human endurance, improve the efficacy of athletic performance etc. 

2. A special protective effect on the heart, can enhance the effectiveness of the heart muscle, causing a reduction in heart disease or cardiac ischemia injury. 

3. At the same time, calcium pyruvate engulfed in a free radicals and inhibit the formation of free radicals and other significant effects. 

4.Some suggest that other potential benefits of calcium pyruvate supplementation may include antioxidant activity for antiaging, lower blood pressure and cholesterol, increased glyogen storage and utilization, 

Effective Dose

The effect of calcium pyruvate may be dependent on the dose, and if you're dieting when you take it. In the "American Journal of Clinical Nutrition" study, participants who took 30 grams of pyruvate, 16 grams of which was calcium pyruvate, were on restricted diets. Pyruvate accounted for 13 percent of the participants' diets. In the study published in "Nutrition," which did not find significant effects for pyruvate, participants maintained their normal diets and took 5 grams of calcium pyruvate twice a day.

Side Effect

However, side effects, such as diarrhea, bloating, gas and increased bowel movements have been recorded. For those with heart disease, be sure to get calcium pyruvate, as compounds stabilized with sodium may increase blood pressure to dangerous levels.

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 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 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.