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BPI A-HD 28 Capsules
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List Price: $56.95
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A-HD™ (formerly known as ARIMEDEX HD™ - name changed
for legal purposes).
A-HD™ is a novel compound Testosterone Boosting Agent. A shut
down non-prescription Anti-Aromatase that works by blocking/binding to
the enzyme aromatase therefore preventing the conversion to 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 A-HD™
A shut down non prescription anti-aromatase that is designed to work by
blocking/binding to the enzyme aromatase, preventing conversion to
estrogen. It's also designed to work 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, dry
looking physique. The ultimate result: no more retaining water, no more
of that bloated look – just rock hard shredded muscle.
What Is Anti-Aromatase?
Anti-aromatase agents are used to block the conversion of aromatizing
AAS (Anabolic/Androgenic Steroids) to estrogen and through binding to
the enzyme aromatase can block the production of estrogens in the body.
Bodybuilders everywhere know that this class of prescriptions taken
during cycles with particular steroids help to avoid any mishaps and
prevent and undesirable hormonal activity. Before any symptoms of
aromatization have occurred at the beginning of a cycle an anti-aromatase
agent can prove most beneficial.
What's in ARIMEDEX HDTM?
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 HDTM 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. |
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| *These statements have not been evaluated by the Food & Drug
Administration. This product is not intended to diagnose, treat, cure or
prevent any disease. |
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