freakazol Information (Prohormones)
Serving Size: 1 capsule
Servings per Container: 60 capsules
Amount per Serving:
13-ethyl-3-methoxy-gona-2,5(10)-diene-17-one - 20mg (LMG)
2a, 17a-di methyl etiocholan 3-one, 17b-ol - 7mg (Superdrol)
4-chloro-17a-methyl-androst-1, 4-diene-3, 17d-diol - 20mg (Halovar)
1 capsule twice daily with meals. Do not take for more than 6 weeks continuously with at least a 4 week break. For oral use only.
At the recommended dosage, you're getting 40mg of Max-LMG, 14mg of Superdrol, and 40mg of Halovar (a Halodrol clone).
TunedSports recommend dosing LMG at 75mg per day for the first half of hte cycle, and 100mg a day for the second, so you're understrength here.
For Superdrol, most users respond well to 20mg a day, and some to even less. In a stack, 14mg is probably OK for most.
Halodrol sweet spot seems to be report at around 75mg a day, again with some users going up to 100mg a day.
And here we kind of see the problem with stacks. Three compounds, two of them severely underdosed, at least according to their use under a standalone protocol.
I still think. if you're going to stack, you're better of building your own.
Also, it's recommending 6 weeks. Seems kind of long to me. Call me an old fart, but a few years back, people ran Superdrol on 3 week cycles, some even on 2! Now here's a company telling you to run 14mg for 6 weeks? Now 14mg might be on the low-ish side, but still... 6 weeks? And then only 4 weeks off? Irresponsible.
General rule I go by is 2x as long off cycle as on. If I do a 5-week Epistane, I take 10 off (the first 3 of that being PCT).
And, when it comes to stack, make your own base dof compounds you've already used and know how you respond to. Sure, it's more expensive, but do you want to risk serious sides to save a few bucks?
13-ethyl-3-methoxy-gona-2,5(10)diene-17-one (Max LMG)Trade names include Max LMG, Tren, Trena, AKA Methoxygonadiene
Common dosage: 60-120mg daily
Common cycle length: 4-6 weeks
Half-Life:Long (48-72 hours)
Not a 17aa steroid so liver toxicity is not as harsh as with 17aa steorids, however the ethyl group on C-18 may make it slightly more toxic than a non-ethylated steroid (while increasing its oral bio-availability). Max LMG is progestin designed to give solid gains in muscle mass with low water retention. The progestational activity of methoxygonadiene (once it is converted to its active metabolites) is considered to be slightly stronger than nandrolone. This means muscle building with Max LMG in your cycle gives you higher quality hardening effects. Since it acts as anti-progesterone, there are decreased negative effects of extra estrogen and increased libido.
It is legal because it is a progestin, like trenbolone, nandrolone, methyltrienolone and Methyl-Dien. As a progestin, Max LMG is structurally related to the pill RU-486 and as such acts as an "anti-progesterone". This results in decreased estrogen-like effects and an increase in libido.
Research suggests that Max LMG has a half-life of about 6 hours, though it appears that it is closer to 10 hours based upon plasma levels maintained in test subjects. It is not a 17-alkylated analog and has a low potential for liver toxicity.
Most users report good results at a dosage of 75mg a day.
Some comments from users:
"As stated, appears to be an all out bulker. Great for size and strength, but notorious for bloat and the potential for gyno. I've also read that it kills libido pretty quickly. Some of the makers claimed that the libido would remain fine if one didn't use too large of daily doses though. I remember seeing people getting decent gains from 40mg - 50mg (depending on the product). It looks like most guys go up to 75mg though."
"Would be my favorite if it didn't make my nips start burning by the end of week two. Rapid weight gain on it plus the fact its not methyl are pluses. Just keep in mind i've seen many complain about it easily aggrevating gyno."
In the stomach acid, the C-3 methoxy group is rapidly cleaved off and the double bond on the A ring at C-2 is lost. At this point, a 3-oxo is formed and a metabolite known as 13b-ethyl-nor-androstenedione is created, which is chemically similar to norbolethone, and probably where this compound gets most of its effects.
13b-ethyl-nor-androstenedione is about equal to testosterone in anabolic potency, yet less androgenic. This would make this compound fairly light on the hairline with minimal chance of acne or other androgenic side-effects.
With low androgenic activity, this compound may negatively affect the libido and erectile function. The lack of androgenic potency and progestational effects make this compound likely to cause gyno symptoms. Users could stack this compound with testosterone or one of its non-aromatizing metabolites to preserve DHT levels and possibly prevent these side-effects.
Users experience rapid weight gain from this compound partly due to subcutaneous water retention from the progestational activity. Therefore the overall gains from this compound may lead to a bloated appearance. Because of the progestational effects, users should avoid stacking this compound with other gyno aggravating compounds. Max LMG can aromatize to estrogen in small amounts, however not to any significant degree, therefore an aromatase inhibitor would provide little protection against this compound's side-effects.
Max LMG immediately converts in the stomach into a 13b alkylated compound (13b ethyl nor androstenedione) and then makes it all the way to the liver because it is ethylated to survive first pass, and is converted into 13b ethyl nor testosterone, a steroid similar to norbolethone aka the clear.
2a,17a-dimethyl-17a-hydroxy,5a-etiocholan-3-one (Superdrol)Seems to be yet another chemical nomenclature for Superdrol:
Superdrol is a powerful anabolic designer steroid brought to market in 2005, however due pressure by the FDA, the original Superdrol was pulled and is no longer available. Like many other compounds, it has been made available again through the production of clones.
4-chloro-17a-methyl-androst-1,4-diene-3-17b-diol (Halovar)A clone of Halodrol (4-chloro-17a-methyl-androst-1, 4-diene-3b,17b-diol)
Halodrol is a 17aa steroid that converts to the steroid oral Turinabol after interaction with 3b-HSD at an estimated rate of about 5%. Because of this low conversion, doses must be higher than other 17aa pro-steroids. However, it is suspected that Halodrol has decent potency without conversion as good results are seen despite the relatively low conversion to Turinabol. Halodrol appears to be about as potent as testosterone, and significantly less androgenic.
Because of the 4-chloro group, halodrol has no progestational effects, it cannot interact with the aromatase enzyme, and it produces inactive 4-chloro-DHT metabolites. This makes androgenic side-effects such as hair loss, high blood pressure, acne and prostate enlargement less likely.
The lack of androgenic potency might be expected to create problems with gyno, however the low SHBG binding affinity has minimal interference with SHBG levels and/or freely circuiting estrogen and testosterone. It does not appear that halodrol has a significant gyno risk.
Because halodrol must be used at such a high dose to see noticeable effects, liver toxicity may become an issue. Therefore it is recommended to use a liver protecting supplement before and during halodrol cycles.
Gains from Halodrol generally take a few weeks to notice, but users can expect solid increases in strength, lean muscle mass, improved vascularity and minimal water retention. This allows some of the gains to be kept after the cycle if good diet and training are continued. Quick dramatic gains in size and strength are not generally noticed with Halodrol.
H-Drol is one of the most popular and proven compounds on the market and is considered good for beginners due to it's reputation for minimal side effects and dry gains that are relatively easy to maintain after the cycle is complete.