6-bromoandrostenedione
CAS: 38632-00-7
Synonyms: 6-BRONMANDROSTENEDIONE;6-bromoandrostenedione;(6b)-6-Bromoandrost-4-ene-3,17-dione
MF: C19H25BrO2
MW: 365.3046
Properties:White Crystalline Powder
Usage :pharmaceutical raw materials, the hormone
Assay: 99%
Appearance: White powder
Usage:the compound 6-Bromodione which binds to the aromatase enzyme making it unable to convert androgens to estrogen.6-Bromoandrostenedione is an androstenedione analog, and an aromatase inhibitor.
6-alpha-Bromodione is a fast acting competitive inhibitor of the aromatase enzyme. It works by binding to the aromatase enzyme to prevent it from aromatizing androgens. This is not a permanent binding and later acts to normalize aromatase (and thus estrogen levels) as hormone production returns to normal. It specifically targets aromatase and does not act as a central anti-androgen like some other post cycle products can. This means that your libido and mood will not be negatively affected.
6-beta-Bromodione works in a similar way but has an irreversible and permanent effect. This works well to mediate the excess aromatase that was produced while on cycle, while the alpha isomer works to normalize the natural levels. The goal is again to transition into normal production levels for all hormones affected by the anabolic cycle.
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Several precursors of testosterone and nandrolone introduced on the nutritional supplement market as performance enhancing drugs are banned in sports. Until now they are legally sold without a prescription in the US. Results of excretion studies with related compounds including 7-keto-DHEA and 1-androstenediol are presented. The main metabolites of 7-keto-DHEA are 7-hydroxylated compounds. The commercial 1-androstenediol preparation was contaminated with several other anabolic steroids. Oxidation of 1-androstenediol to 1-androstenedione seems to be the major renal metabolic pathway. Additionally contaminated nutritional supplements containing banned substances not indicated on the label were administered. The results of the excretion studies indicate that after the intake of amounts substantially lower than the recommended dose athletes can fail a doping test for periods up to 120 h.
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