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February
23, 2001
Issue
# 35
THE
FUTURE OF PROHORMONES IS 1-AD
by
Pat Arnold

In
Pursuit of the Holy Grail
You
are about to be introduced to the future of prohormones.
It is called 1-AD, and it is without a doubt the single most
amazing prohormone to be synthesized and sold as a nutritional
supplement.
Let
me start by setting something straight.
We are not amateurs to the prohormone industry.
On the contrary, we actually started the whole prohormone
industry. But not only that, we are also responsible for practically
every significant innovation in prohormone technology to date.
The leader of Ergopharm, organic chemist Patrick Arnold, was
the person who discovered androstenedione and introduced it to the
market in 1996. Patrick
also discovered and patented androdiol® (4-androstenediol) and
norandrodiol™ (19-nor-4-androstenediol), and introduced
cyclodextrin technology to the prohormone industry.
For
the past 18 months Patrick has feverishly been working - almost
exclusively - on one project. While
scores of less knowledgeable people in the industry periodically
made occasional lame, foul ball attempts at finding the “latest,
greatest” prohormone, Patrick kept quiet and worked on the
development of what essentially could be called the “holy grail”
of prohormones.
Patrick
wanted this prohormone to have all the attributes most critical to
the perfect prohormone. It
was to be:
After
months of scouring every book and journal he could locate, including
those in foreign languages (i.e. German), Patrick discovered a
compound that seemed to be the perfect candidate.
That was the easy part.
It then took Patrick almost one whole year to figure out how
to manufacture the compound cheaply enough for sale as a supplement.
Patrick’s lab took on the appearance of ground zero at
Hiroshima as he endlessly did reaction after reaction in pursuit of
the perfect manufacturing recipe.
.
Ergopharm’s
pledge
Before
I introduce exactly what 1-AD is, I want to mention one quick thing.
In this industry it’s often hard to find straight answers to
exactly what something is, and how something works.
Most often, the case is that the company is evasive with the
facts because there really is no existing science that validates the
claims they are making. Either
that, or they simply do not understand the science themselves.
Occasionally a company does have science to back up their
products, but they decide that the consumer is too simple minded to
appreciate the facts.
Ergopharm
is different. We
produce products that are backed up by hard scientific fact, and we
take great pride in laying everything on the table. Our strength is our science, and we go to great lengths to
explain all the facts and back them up with references.
We understand that not everyone buying our products has a
chemistry or biology degree, but we do know that people appreciate
being treated with respect and honesty. They want to know they are being told the straight story,
even if they don’t have the background to understand every facet
of the presentation.
Introducing
1-AD
Its
time to introduce what Patrick refers to as “the crown
achievement” of his career. The
formal chemical name of the compound Patrick developed is 5alpha-androst-1-en-3,17-dione.
We nicknamed this compound “1-AD” which is a shortened
acronym of its chemical name. Its chemical structure is:
This
compound is truly unique amongst other prohormones in a variety of
ways. Lets look
specifically at 1-AD and what it does.
.
The
Power of “1-Testosterone”
You
probably are familiar with the “Andro” prohormones, and the
“Norandro” prohormones. The
former convert to testosterone and the latter to 19-nortestosterone.
1-AD, however, does not fit into either of those categories.
That is because 1-AD converts to a relatively unheard of
hormone called 1-testosterone.
1-testosterone is what is known as a “double bond isomer”
of testosterone.
Although
chemically the only difference between testosterone and
1-testosterone is position of the double bond, pharmacologically the
two products are quite different.
According to research done by the pharmaceutical giant G.D.
Searle and published in the 1960s, 1-testosterone is over 7 times as
myotrophic (anabolic) as testosterone.[i]
That makes 1-testosterone a phenomenally potent compound,
surpassing even most synthetic anabolic steroids.
.
No
Aromatization
1-testosterone
differs from testosterone in another way as well. Being a
5alpha-reduced androgen (a DHT derivative) it simply cannot
aromatize to estrogens. The same goes for 1-AD itself - no estrogen
transformation can occur. This
makes 1-AD unique compared to other prohormones - all of which can
either aromatize directly, convert to a product that aromatizes, or
both. So what does this
mean in the real world? It
means that your chances of getting gynecomastia (bitch tits) from
1-AD is essentially zero, and that water retention side effects are
vastly reduced compared to other prohormones.
.
The
Only Truly “Orally Active” Prohormone
Natural androgenic
steroids are normally not very active orally.
Large amounts have to be taken orally to see biological
effects. This is because the liver first pass causes a massive
deactivation of the compounds, primarily through the oxidation of
the 17beta-hydroxyl to a 17-keto group.
Chemists long ago found that by adding an alkyl (methyl or
ethyl) chemical group to the alpha position of the 17 carbon, this
oxidation can be prevented. However,
this alkyl derivatization also greatly increases the toxicity on the
liver. Therefore the
usage of such synthetically altered compounds (methyltestosterone,
oxymetholone, stanozolol) are not without substantial risk.
Luckily,
there are other ways to render a steroid orally active, and do so
without making the compound toxic to the liver.
Certain structural modifications can alter the metabolism of
steroids making them resistant to liver breakdown.
One of these modifications is unsaturation (presence of a
double bond) in the 1-position.
One steroid that has this structural modification and is
orally active is the anabolic steroid Methenolone, also known as
Primobolan.
As
you may have noticed, this double bond position that makes
Primobolan orally active is the same one found in 1-AD, which BTW is
also orally active. Steroids
with this particular double bond characteristic are known as
1-dehydroandrostanes.
During
the 60’s and 70’s some papers were published describing the
phenomenon of oral activity seen with 1-dehydroandrostanes,
including 1-testosterone and 1-AD.
What was discovered was that these compounds resist metabolic
deactivation by profoundly shifting what is known as the “17-keto
redox potential” towards the formation of active 17beta-hydroxyl
steroids.[ii],[iii]
What does this mean? It
means that when you take 1-AD, the liver serves primarily to
activate the compound, rather than break it down and excrete it as
it does with other prohormones and testosterone.
It means that 1-AD is “orally active,” yet it does not
impart the liver toxicity that 17alpha-alkylation does.
.
A
Natural Hormone Made in the Body
One
of the beautiful things about 1-AD is that in addition to its
impressive pharmacological activity, it is also a natural androgen
made in the human body[iv].
This means that it is not foreign to your body, and that it
can legally and openly be sold as a nutritional supplement.
Furthermore, 1-AD’s high rate of active conversion after
oral administration is not just a “theory” of Ergopharm’s –
it has been demonstrated and published in a highly reputable peer
reviewed journal.[v]
.
Summary
Lets
put it all together and see what 1-AD has to offer:
There
can be no argument that this is the ultimate prohormone.
Believe me, there simply are no natural compounds out there
that can come close to what 1-AD does, so don’t even bother
looking.
[i]
Counsel et al., “Anabolic Agents.
Derivatives of 5alpha-Androst-1-ene”, J. Org. Chem., 27
(1962), 248-251
[ii]
Galletti and Gardi, “Metabolism of 1-Dehydroandrostanes in
Man”, J Steroid Biochem, 3 (1972), 933-936
[iii]
Langecker, “Beziehungen Zwischen Substitution im Ring A und
Abbau im Stoffwechsel bei Verwandten des Testosterons”, Acta
Endocrin, 41 (1962), 494-506
[iv]
Lieberman et al., J. Biol. Chem, 182 (1950), 299
[v]
Galletti and Gardi,
“Metabolism of 1-Dehydroandrostanes in Man”, J Steroid
Biochem, 3 (1972), 933-936
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