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Επιστροφή στο Forum : A-HD (Bpi Sports)



poison1
02-04-12, 20:55
A-HD

JUST ONE ULTRA CONCENTRATED CAPSULE PER DAY
TESTOSTERONE BOOSTER
ANDROGENIC AND ESTROGENIC MODULATOR
#1 PCT (Post Cycle Therapy)

42680

42681


Introducing A-HD™ the ultimate estrogenic modulator and androgenic formula! A-HD™ is designed to support increased testosterone production while minimizing estrogen activity. 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! A-HD is the androgenic/estrogenic modulator of choice, as well as the top PCT (post cycle therapy), among all hardcore bodybuilders in the "know". Ever wonder how to get that long lasting, hard-as-nails, dense, muscular look? This is it. A-HD is The Ultra Concentrated Testosterone Booster. Just one small capsule a day. That's it. Not 2-4 capsules at a time. Don't waste your time with anything else because THERE IS ABSOLUTELY NOTHING LIKE A-HD™

What’s in A-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:
Scientific evidence shows that this novel lignan-class compound has potent anti-estrogenic activity.

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:
Scientific evidence shows that this compound possesses powerful anti-estrogenic properties via multiple mechanisms.* Specifically, this novel lignan-class compound has been shown to 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 may help 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:
Scientific evidence 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, healthy glucose metabolism, and maintaining healthy 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:
Scientific evidence 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: Scientific data 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:
Scientific evidence shows that this remarkably active, 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.*


Suggested Usage: Take one (1) capsule daily, (in the morning) at the same time each day, or as directed by a qualified healthcare practitioner. Must be taken on a full stomach. For best results take four to eight (4-8) consecutive weeks (1-2 Cycles). Do not take this product longer than eight (8) consecutive weeks. A four (4) week break between cycles is recommended.


Serving Size 1 Capsule
Servings Per Container 28
Amount Per Serving % Daily Value
Niacin (as Nicotinic Acid) 25 mg (125% DV), A-HD™ Proprietary Blend 250 mg (* DV), (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,(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,s)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-decanone. Standard Phytochemical Complex Blend 30 mg (* DV), 4-[(e)-2-(3,5-dimethoxyphenyl)ethenyl]phenol, Curcuma longa (rhizome), Cynara scolymus (leaf),phenethyl(e)-3-(3,4-dihydroxyphenyl)prop-2-enoate.
*Daily Value not established.
Other Ingredients: Gelatin, Microcrystalline Cellulose, Magnesium Stearate, Silicon Dioxide, Hypromellose, Polyvinylpyrrolidone, Maltodextrin, Stearic Acid, Capsicum annuum, FD&C Blue #1, Titanium Dioxide.





καταρχην 1000 συγνωμη αν υπαρχει εκανα αναζητηση αλλα δεν εβγαλε τιποτα, ουτε και με την παλια ονομασια
καμια γνωμη??? εγω παντως ενιωσα χαμενος στη μεταφραση:green:

beefmeup
03-04-12, 11:37
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:



ειναι αυτο trechaloside.


An anti-estrogenic lignan glycoside, tracheloside, from seeds of Carthamus tinctorius.

Yoo HH, Park JH, Kwon SW.

College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
Abstract

The lignan glycoside, tracheloside, was isolated from seeds of Carthamus tinctorius (Compositae) as an anti-estrogenic principle against cultured Ishikawa cells by employing a bioassay-linked HPLC-ELSD method. Tracheloside significantly decreased the activity of alkaline phosphatase (AP), an estrogen-inducible marker enzyme, with an IC(50) value of 0.31 microg/ml, a level of inhibition comparable to that of tamoxifen (IC(50) = 0.43 microg/ml).


(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

ειναι αυτο..Secoisolariciresinol diglycoside...
φυτοσοιστρογονο ειναι λενε..

4-[(e)-2-(3,5-dimethoxyphenyl)ethenyl]phenol

ειναι αυτο..Pterostilbene
ξαδερφακι της ρεσβερατρολης..


-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-decanone

ginger..το γνωστο.


phenethyl(e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

ειναι αυτο..Caffeic Acid phenethyl ester
δλδ ειναι η γνωστη προπολη??

Phytother Res. 2010 Feb;24(2):295-300.
Caffeic acid phenethyl ester, a component of beehive propolis, is a novel selective estrogen receptor modulator.

Jung BI, Kim MS, Kim HA, Kim D, Yang J, Her S, Song YS.

College of Pharmacy, Sookmyung Women's University, Seoul, Republic of Korea.
Abstract

Caffeic acid phenethyl ester (CAPE) is an active ingredient of beehive propolis with a structure similar to phenolic acid. The estrogenic effects of propolis were previously demonstrated through the activation of an estrogen receptor. To identify the estrogenic properties of propolis, CAPE was evaluated using in vitro and in vivo methods. CAPE showed selective binding affinity to human estrogen receptor beta (hERbeta) rather than hERalpha. CAPE also reduced ERalpha expression in MCF-7 and MDA 231 cells. In the yeast estrogen receptor transcription assay, CAPE produced the transcriptional activity of estrogen-responsive element with EC(50) values of 3.72 x 10(-6) M. CAPE did not increase the growth of MCF-7 estrogen receptor-positive breast cancer cells in doses ranging from 10(-7) to 10(-5) M. In order to understand how CAPE acts in animals, CAPE was tested by a uterotrophic bioassay. Treatment with CAPE (100, 500 mg/kg) did not increase the uterine weight relative to 3 microg/kg 17beta-estradiol treatment. The results indicate that CAPE, which is a selective agonist to hERbeta, but does not show any estrogenic effect on estrogen receptor-positive breast cancer cells and in immature rat uterine tissue, is a potential selective estrogen receptor modulator. (c) 2009 John Wiley & Sons, Ltd.


τα σχολια ειναι περιτα νομιζω...:green:

zisgeo
03-04-12, 23:10
δηλαδή αξίζει ή όχι? σκεφτομαι να χρησιμοποιήσω αυτο το stack της bpi sports : A50 (60 caps), Solid (28 caps) & A-HD (28 caps)

Devil
03-04-12, 23:18
δηλαδή αξίζει ή όχι? σκεφτομαι να χρησιμοποιήσω αυτο το stack της bpi sports : A50 (60 caps), Solid (28 caps) & A-HD (28 caps)

με απλα λογια..... ΟΧΙ...:green:

zisgeo
04-04-12, 12:50
μαλλον ειναι λίγο off απο το θέμα, αλλά για πρωτο κύκλο ανάλογο με τον παραπάνω τί προτείνετε?