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Methyl-1-Testosterone, a.k.a. methyldihydroboldenone, is a methylated derivative of the anabolic steroid dihydrotestosterone (DHT), an anabolic steroid that was designed to treat testosterone deficiency in males.

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This 3 FPM and Mexedrone Combo Pack puts 2 of our best selling stimulants in a combo pack! These 2 products combined give the best lab results recorded.

Mexedrone is supplied in a pure white powder and is not crushed crystal, but is genuine mexedrone powder. Mexedrone is an analogue of MMC. It's full chemical name is 3methoxy-2 (methylamino)-1-(p-tolyl)propan-1-one or also known as 4-mmc-oMe.

3 FPM's chemical name is 3-fluorophenmetrazine, is the 3-fluoro analogue of Phenmetrazine. Phenmetrazine was an extremely popular chemical with researchers in the 1960s, with in-vitro stimulant properties

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3 FPM & Mexedrone Combo is not for human consumption.
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Aditpotide is an experimental weight loss peptidomimetic with the amino acid sequence CKGGRAKDC-GG-D(KLAKLAK)2, which has been developed by researchers in the United States in an effort to fight obesity. Peptidomimetics are small protein-like chains designed to mimic a peptide. The peptide called Adipotide has been developed by U.S. researchers in the fight against the obesity . This experimental treatment has reduced by 11% the weight of the treated monkeys by reducing fatty tissue, the BMI, and waist circumference.

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Currently, AICAR has also been shown as a potential treatment for diabetes by increasing the metabolic activity of tissues by changing the physical composition of muscle.  AICAR (commonly under the name Acadesine) is an analog of adenosine that enters cardiac cells to inhibit adenosine kinase and adenosine deaminase. It enhances the rate of nucleotide re-synthesis increasing adenosine generation from adenosine monophosphate only during conditions of myocardial ischemia. In cardiac myocytes, AICA-riboside is phosphorylated to AICA-ribotide (ZMP) to activate AMPK without changing the levels of the nucleotides. ZMP is able to enter the de novo synthesis pathway for adenosine synthesis to inhibit adenosine deaminase causing an increase in ATP levels and adenosine levels.

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