| What is ARIMEDEX
HD™? Arimedex HD™ is a novel compound Testosterone Boosting
Agent. A shut down non-prescription Anti-Aromatase Inhibitor that works
by blocking/binding to the enzyme aromatase therefore preventing the conversion
of Estrogen. It also works by binding to the estrogen receptors and by
doing so, prevent harmful estrogen from binding to these receptor sites.
ZERO to little Estrogen leads to a harder, leaner, more dry looking physique.
No more holding water, no more bloated looks – just rock hard shredded
muscle.
THERE IS ABSOLUTELY NOTHING LIKE ARIMEDEX HD™
Anti-Estrogenic? These are used for blocking receptor sites, not to stop
conversion of aas to estrogen. When it is already converted, anti-estrogens
keep the body from performing this action. The anti-estrogens need to
be taken before and at the first sign of receptor activity (gynecomastia),
or to supplement with an aromatase inhibitor.
Anti-Aromatase? Used to block the conversion of aromatizing aas to estrogen,
and through binding to the enzyme aromatase, can block the production
of estrogens in the body. Bodybuilders everywhere are using this class
of drugs during cycles with particular steroids, this will avoid any mishaps
to prevent any undesirable hormonal activity. Before any symptoms of aromatization
have occurred at the beginning of a cycle, take anti-aromatase.
What’s in ARIMEDEX HD™? CHEMICAL NAME: (3s,4s)-4-[(3,4-dimethoxyphenyl)methyl]-3-hydroxy-3-[[3-methoxy-4-[(2s,3r,4s,5r,6r)-3,
4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-phenyl]methyl]oxolan-2-one:
Research shows that this novel lignan-class compound has potent anti-estrogenic
activity, with a potency factor comparable to the leading anti-aromatase
prescription intervention. Arimedex HD™ is the first dietary supplement
product to feature clinical dosed levels of this anti-estrogenic compound.
CHEMICAL NAME: (2r,3r)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl] butane-1,4-diol;(2r,3r,4s,5s,6r)-
6-(hydroxymethyl)oxane-2,3,4,5-tetrol: Research shows that this compound
possesses powerful anti-estrogenic properties via multiple mechanisms.
Specifically, this novel lignan-class compound has been shown to inhibit
aromatase (it also shows synergistic/additive effect when taken in combination
with the leading anti-aromatase prescription intervention), inhibit 3ß-hydroxysteroid
dehydrogenase and 17ß-hydroxysteroid dehydrogenase, down-regulate
5 alpha-reductase, modulate tyrosine kinases as well as other protein
kinases, and favorably modulate plasma free testosterone levels. Moreover,
use of this compound prior to sustained physical exercise/exertion helps
to reduce muscle damage via up-regulation of hepatic glutathione (GSH)
levels and down-regulation of malondialdehyde (MDA) levels in skeletal
muscle.
CHEMICAL NAME: 4-[(e)-2-(3,5-dimethoxyphenyl)ethenyl]phenol: Research
shows this novel stilbenoid-class compound, which is methylated, is markedly
more efficiently metabolized than non-methylated stilbenoid-class compounds
for activation of the SIRT1 gene, up-regulation of plasma free testosterone
production via selective estrogen receptor (ER) modulation, inhibition
of aromatase, enhanced glucose metabolization, and improved insulin sensitivity.
As a methylated stilbenoid-class compound, this compound is not sulfated
by P450 enzymes, which translates into significantly greater bio-activity.
CHEMICAL NAME: s)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-decanone:
Research shows that this phenolic-acid class compound exhibits bio-active
androgenic activity via multiple pathways, such as marked down-regulation
of malondialdehyde (MDA) levels, resulting in potent potential up-regulating
effects on plasma free testosterone and luteinizing hormone. (NOTE: One
published study showed an increase of up to 231.8% in plasma free testosterone
(as compared to control), and an increase of up to 147.6% in luteinizing
hormone (as compared to control).)
CHEMICAL NAME: phenethyl(e)-3-(3,4-dihydroxyphenyl)prop-2-enoate: Research
shows that this remarkably active, potent and specific phenolic acid-class
compound blocks inflammatory proteins, such as pro-inflammatory interleukin-1{beta},
and also inhibits prostaglandin synthesis in acute inflammation, and suppresses
COX-II mRNA and protein. This compound is a specific inhibitor of 5 alpha-reductase
(which down-regulates conversion to dihydrotestosterone) activity. Moreover,
this compound acts as an estrogen receptor (ER) modulator.
ARIMEDEX HD™ is The Ultra Concentrated TESTOSTERONE Booster. It
is a single capsule dose. That’s it. Not 2-4 capsules daily. Just
ONE SINGLE CAPSULE daily.
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