Tren is back?!
- 05-09-2010, 06:45 PM
- 05-09-2010, 06:53 PM
- 05-09-2010, 06:54 PM
05-09-2010, 06:57 PM
05-09-2010, 07:00 PM
05-09-2010, 07:01 PM
05-09-2010, 07:10 PM
05-09-2010, 07:14 PM
theres a risk of gyno from using anything hormonal. progestins are just commonly associated with Prolactin induced gyno. proper pct and cycle supports youd be fine
05-09-2010, 07:15 PM
Hmm...yeah I want to avoid anything like that because I think I am very prone to gyno. Thanks mball52.
05-09-2010, 07:17 PM
05-09-2010, 09:08 PM
the chance of gyno is about the same with pro dienolone (tren ph) as it is with max lmg. and they aren't progestins, they are steroids that bind to the androgen receptor, as well as have some activity on the progestin receptor, there by possibly enhancing estrogenic sides.
gyno is caused by multpile hormone imbalances, to narrow it down to a specific hormone imbalance, is difficult, even with blood test.
stacking max lmg or pro dienolone with something like dht will help with the sides.
I used pstanz recently, others use pro dht. more common is epistane.
Olympus Labs Rep in the UK ;)
05-09-2010, 10:26 PM
05-09-2010, 10:32 PM
05-09-2010, 10:46 PM
All I know is I didnt like my experience with Revolt(13-ethy) so others can have that while I go admire my stash
05-10-2010, 12:36 AM
It is a progestin, but because it’s structurally related to RU-486 – the structure of which is in the figure below –
It works primarily as a progesterone blocker. It is not C-17 methylated, so it’s not dangerous for the liver, and it makes you grow serious muscle bulk.
What more do you want?
It’s a great story. If we draw the formula of the compound 13-ethyl 3-methoxy 2,5(10)-gona-diene 17-one, with our limited understanding we don’t get anything that even vaguely resembles RU-486. We stumbled on the steroid shown on the left in the diagram below.
The A-ring looks suspiciously like that of estradiol. In an acid environment, like in the stomach, the A-ring changes. The methoxy group on C3 falls off and a double bond disappears. See the right-hand side of the diagram.
Then, still in an acid environment, the double bond shifts in the molecule. See below.
Enzymes in the body then change the carbonyl group on C17 into a hydroxyl group. The end result is an androgen that has little resemblance to RU-486,
but is similar to norbolethone, Balco’s first undetectable hormone. The structure of norbolethone is drawn below.
Whether the substance has any effect, and whether it is safe, has never been studied.
this is the most data based research on max lmg i can find, as it is a vauge compound, that has info as limited as the compound found in protodrol.
but from what I know about this product, though the nomenclature makes it looks like a progestin, when we draw out the compound, is in fact an anabolic pro steroid.
Olympus Labs Rep in the UK ;)
05-10-2010, 01:28 AM
05-10-2010, 11:52 PM
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