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1. What is it and where does it come from?

Methyl-1-4-OHN (4-Hydroxy-17aMethyl-Hydroxyestra-4ene-3-one) is a potent prosteroid, similar in chemical configuration to Deca Durabolin (nandrolone decanoate).

2. What does it do and what scientific studies give evidence to support this?

Because this substance is relatively new, anecdotal reports are mixed.

Prohormones Banned Jan. 20th, 2005

On January 20th, 2005 the US Federal Gorvenment's ban on prohormones took effect. Don't worry though, we have numerous other products that work just as well. Find out more about these alternatives.

Methyl-1-4-OHN is similar in chemical structure to nandrolone decanoate and is believed to deliver similar results. Reported results include increased feelings of well being, improved joint function, reduced body fat levels and increases in muscular hypertrophy.

Users have also indicated that methyl-1-4-OHN is similar to, but up to 10x more powerful than, the hardening drug oxandrolone. Methyl-1-4-OHN may also be very angiogenic - meaning that it may increase vascularity.

Users of Methyl-1-4-OHN consistently report that it is effective at eliciting muscular hypertrophy and strength.

The chemical structure of methyl-1-4-OHN makes it resistant to aromatization.¹ In addition, Methyl-1-4-OHN will not convert to dihydrotestosterone or dyhdronandrolone. This offers anabolism without estrogenic side effects.

This page will be updated as data becomes available.

No physiological need for Methyl-1-4-OHN exists and thus no symptoms of deficiency exist.

Methyl-1-4-OHN is of benefit to athletes and bodybuilders, as well as any male person free of medical complication looking to increase quality of life and physical health.

Females should not use this product.

Strictly adhere to label recommendations.

Anecdotal evidence indicates that side-effects are limited and rare.

With any prohormone or prosteroid product, endogenous down-regulation of testosterone production is likely. Anti-estrogen products used post-administration may prove efficacious.

REFERENCES

1. Rubin et al. Endrocrinol., 49, 1951, p. 429.