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  • Country/region: China
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4-DHEA

  • CAS No:853-23-6 Dehydroepiandrosterone acetate
    Molecular Structure

    Detailed Description

    4-DHEA is a naturally occurring unmethylated (non-17aa) steroid.

    4-DHEA, such as DHEA, requires a two-step conversion process involving 3b-HSD and 17b-HSD to convert it to androstenedione / maleenediol, followed by testosterone. DHEA is slightly different from the 4-DHEA is the fourth and not the fifth of the double key. This allows 4-DHEA to reduce estrogen by not directly acting on estrogen receptors (such as DHEA has been found).

    Although 4-DHEA can cause estrogenic fermentation, it may not be sufficient to cause high estrogen-related side effects.

    The overall results will be similar to the original 4-AD disabled in 2004. Higher doses of this compound will produce considerable lean gain in muscle mass, with improved strength. The product may be partially inflated by estrogen conversion, which may be counteracted by administration of an aromatase inhibitor, but this will greatly disrupt the use of the compound for the purpose of initiation.

    Since this compound is naturally occurring and unmethylated, the overall side effect will be quite mild. However, high doses may also cause oily skin, acne and elevated blood pressure. Because this steroid is non-17aa, the negative effects on low-density lipoprotein / low-density lipoprotein ratio should be less.

    Because this compound can be converted to testosterone, it can also be converted to DHT and other 5α-reduced metabolites. This can be a good stack with progesterone or relative non-androgenic compounds, which may cause sexual or female problems due to lack of androgenic potency.


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