Strength steroids like Masteron, Anavar and Anadrol all share one thing in common, they are Androstanes. The Androstane skeleton is key for steroids that provide increased fat loss and increased strength like Masteron, Anavar, Anadrol and many others including Winstrol. Methyl Masterdrol V2 is a true DSHEA legal prohormone with this amazing amdrostane skeleton and the Methyl-Block delivery system, making it the most advanced prohormone on the market for cutting fat and increasing strength. Like I said, Steroids like Proviron, Masteron and Anavar are androstanes and have the same skeletal structure as our new Methyl Masterdrol V2 V2 and they have the exact same molecular weight skeleton. This is why we chose androstane to be our horse and Ester with Methyl Block™ to be our delivery system, like we did with 17aa - Methyl 1-Test, Methyl 1-P and Masterdrol V2.
Benefits of Prohormones Over Steroids:
Zero Liver Toxicity!
Legal DSHEA Compliance
Reduced risk
Slow growth that is easier to keep
We also used the newsest quick release technolgy in our XPLO caps, which allows reapid release and quick delivery of the amazing androstane in Methyl Masterdrol V2. XPLO caps disolve quickly and increase the absorption rate of the androstanes which give immediate agression and performance enhancement in the gym which is why they are best taken 20-30 minutes bedfore a workout. This means more intense workouts and increased agression…focus to power past your plateaus and squeeze out that extra rep!
Making Prohormones MORE Effective:
The added support ingredients increase the effectiveness of Methyl Masterdrol V2 simulating the Methyl delivery system without any liver toxicity.
Piperine: bocks sulfotransferase, the main enzyme for clearing our Androstane from the intestines.
Zinc Asperate: Increases hormonal activity at the cell
Caprylic Acid: Increases androgen receptor activity, making the hormones more potent
Coleus Forskolin: Increases 3bHSD making the conversion to active stanolone more effective.
Yohimbine: Increases intensity of Masterdrol’s central nervous system stimulation.
The effect of Androstanes
In looking at the literature, you find that many androstane based steroids are usually deactivated in muscle, which is why you can’t just buy any product thrown together without the HEAVY science behind it. Proviron solves this problem by methylating the 1 postion, Masteron solves this issue by methylating the 2 position as did the old Methyl Masterdrol V2. What did this teach us? If you can prolong the half life of the androstane skeleton, stabilize the 3 position and give an effective dose, you can get the SAME results which is pretty damn cool. You need a good dose of androstane ester, but that’s why we gave you 300mg per serving more than 3X any other prohormone EVER made. How does it work? First, the ester protects the molecule and VASTLY increases it’s half life in the body by being metabolized more slowly by esterase. Which also blocks 3bHSD in the liver. Longer half life is the secret of Methyl steroids and makes Methyl Masterdrol V2 so potent and effective. We were not satisfied there though, we then added our Methyl Block technology that boosts half life even further and adds potency by blocking liver destruction, sufatase and glucoronidase enzymes along with upregulating 3bHSD to convert more of the base prohormone into an active steroid. Combined, Methyl Block and Ester make for ONE HELL OF A PRODUCT that we can be proud to call Masterdrol!
Kick back and let me explain why Methyl Masterdrol V2 is the most advanced product of its kind and why the people that doubted the AMAZING LG Sciences, get the proverbial SMACKDOWN once again in the science department.
Big Myth #1 “The liver destroys prohormones”….WRONG!
I don’t blame you, I believed it too. “They” told us “The liver is the enemy…the first pass metabolism is what destroys prohormones and converts them into useless metabolites vs. active prohormones.” Remember? We have all read how Testosterone orally is ineffective because of the liver destroying it… In fact some people tell you to drink grapefruit juice or take some useless grapefruit extract to deactivate the liver enzymes, so a few precious milligrams of ACTIVE hormone can get through. Oh, they also came up with this BULLSHIT lymphatic delivery crap too, that we all bought into as a way to increase the bioavailability of hormones.
What if I could show you how our ANDROSTANE derivatives in Methyl Mastrdrol actually get converted to STANOLONE derivitives in the stomach and that the STOMACH and INTESTINE are actually what causes the problems with old prohormones, not the liver? Also I am going to show you how we used turned those findings into a system that works in reverse. What used to disable the old prohormones is the same system we use to ACTIVATE our ANDROSTANES. I am about to do just that for you!
It’s not the liver that causes the issues it’s the “gut” or intestinal systems! To quote a study “Our findings suggest that the gut, rather than the liver, is responsible for the failure of oral testosterone to provide effective androgen replacement therapy.”
Testosterone metabolism by the rat gastrointestinal tract, in vitro and in vivo.
· Farthing MJ,
· Vinson GP,
· Edwards CR,
· Dawson AM.
We have shown previously that the capacity of the jejunal mucosa to oxidise testosterone to the weaker androgen, androstenedione, by the enzyme 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD), is considerable. The present study extends these earlier observations by measuring 17 beta-HSD activity in different regions of the gastrointestinal tract, by investigating the potential for testosterone metabolism by slices and everted sacs of rat jejunum, and estimating the contribution of intestinal testosterone metabolites to circulating levels of plasma androgens, by portal vein sampling in the rat, in vivo. 17 beta-HSD activity in homogenates of gastric and duodenal mucosa was significantly higher than that in jejunum, and was also present in ileum and colon. In addition to androstenedione, slices and everted sacs of rat jejunum produced various metabolites, one of which was probably dihydrotestosterone. It was not, however, a major metabolite in vivo. It is suggested that 5 alpha-reduction may be favoured in vitro by a lower oxidation-reduction potential resulting from tissue anoxia. The major portal vein metabolite was androstenedione, the same major metabolite produced by mucosal homogenates. We conclude that oxidation of testosterone is the major metabolic pathway in intestinal mucosa and the capacity of the gastrointestinal tract to reduce the potency of testosterone is considerable. Our findings suggest that the gut, rather than the liver, is responsible for the failure of oral testosterone to provide effective androgen replacement therapy. The qualitative difference in testosterone metabolism between in vitro and in vivo preparations emphasises the need for caution in the interpretation of similar in vitro experiments.
What if we show you how by doing the OPPOSITE of what the “experts” told you, you could get more ACTIVE HORMONES in your body??? IMPOSSIBLE? To quote Kramer from Seinfeld “is it so possible that I just blew your mind?” So, the “so called” experts tell us we need to find better ways of making WRONG hormones more active, when actually we can feed the RIGHT hormones into the body and let it take its own natural course of conversion to PURE ACTIVE ANABOLICS!
Methyl Masterdrol V2’s end hormone Stanolone is 400% more anabolic than testosterone!
If you take the “old school” prohormone products, you got very little active in the muscle, where active is defined as something that builds muscle (3-one, 17b-ol steroids):
Oral Stanolone (illegal active steroid) + Gut Enzymes (17bHSD) = Androstanedione (inactive prohormone) + Liver/Muscle Enzymes (3bHSD) = Androsterone (inactive prohormone)
Oral Androstanedione (illegal inactive prohormone) + Gut Enzymes (17bHSD) = Stanolone (active steroid) + Liver/Muscle Enzymes (3bHSD) = Androstanediol (inactive prohormone)
Oral Androstanediol (illegal inactive prohormone) + Gut Enzymes (17bHSD) = Androsterone (inactive prohormone) + Liver/Muscle Enzymes (3a/3bHSD) = Androstanedione (inactive prohormone)
So, you can see that with the prohormones of old, you get INACTIVE hormones in the muscle no matter what path you take, EXCEPT for Methyl Masterdrol V2’s Androstane ester:
Methyl Masterdrol V2 Androstane Ester (DSHEA compliant prohormone) + Gut Enzymes (17bHSD) = Androstanediol (prohormone) + Liver/Muscle Enzymes (3a/3bHSD) = Stanolone (ACTIVE STEROID)
The cool thing is that Stanolone is 400% more anabolic than Testosterone!
ONLY Stanolone Builds Muscle and is 400% more anabolic than Testosterone! The only way to get STANOLONE in the muscle is with Methyl Masterdrol V2! Yet again we lay the smack down on the competition.
THIS IS THE SECRET BEHIND THE NEW METHYL MASTERDROL V2
I hope this wasn’t too complicated, but I wanted to show you how we OUTSMART them again with our Androstane and give you EXACTLY what you want in a supplement, something that works! The people you “thought” were the experts are working off the old theories from 8-10 years ago and that is why we have dominated the prohormone market for over 3 years!
Linear Mode
