LG Sciences (Formerly Legal Gear) METHYL MASTERDROL V2 Supplement
Information
LG Sciences [Legal Gear], originally sky rocketed to world fame by releasing
onto the sports supplement market, M1T [methyl-1-testosterone]
- the compound that rapidly became the fastest selling and effective OTC
pro-hormones available. This exciting development company have
continued to research the very latest, cutting edge compounds in physique
development and LG Sciences [Legal Gear] offer a truly exceptional and
diverse range of designer physique development agents.
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
androstane 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:
* Legal DSHEA Compliance
* Reduced risk
* Slow growth that is easier to keep
We also used the newest quick release technology in our XPLO caps, which
allows rapid release and quick delivery of the amazing androstane in Methyl
Masterdrol V2. XPLO caps dissolve quickly and increase the absorption
rate of the androstanes which give immediate aggression and performance
enhancement in the gym which is why they are best taken 20-30 minutes
before a workout. This means more intense workouts and increased aggression…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 position, 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 up regulating
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 derivatives 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 oxidize
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 favored 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 emphasizes 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!
Supplement Information LG Sciences METHYL MASTERDROL V2 (Formerly
Legal Gear) - Creators of the original M1T
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