ORAL ONLY CYCLE THAT WORKS! Can you take an oral only cycle?

Dean Destructo

Dean Destructo

New member
YES

There is one exception to the rule, and that is SUPERDROL



AKA: Dimethazine (DMZ), M Drol , mathasteron, methyldrostanalone


2a,17a-dimethyl-5a-androst-3-one-17b-ol​

Dosing:

Superdrol (currently not legal)20-40mgs Daily
DMZ (currently "grey area") Can be legally purchased.45-60mgs Daily
Cycle length5 weeks Max

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PCT:

Noladex: 20mgs ED for 4-6weeks
Clomid: 150mgs ED for 4-6 weeks
OR-
Nolvadex and Clomid:
20mg Nolvadex ED
50mg Clomid ED
Both for 4 weeks.

This oral designer steroid hit the market in 2005. It is very similar to masteron. It is actually based on masteron. This compound was actually first synthesized in 1959, at the same time as Masteron and Anadrol. It is no longer legal to posses superdrol, in its original form. You CAN BUY it LEGALLY in it's stereochemetistry version Dimethazine.

DMZ can be purchased legally, online. There are also UG brands of the original superdrol, I believe Geneza pharms produces some. (NOT A SOURCE, A BRAND)

What is the difference between DMZ and original superdrol. Not much. DMZ is basically two superdrol molecules bonded together, the bond is easily cleaved in the stomach thus laving free 17aa drostanalone in the blood. Due to the added Azine structure though, more DMZ vs superdrol will be needed. For example 45mgs DMZ equals ~20mgs superdrol.

Superdrol and all of it's variants are hepatotoxic! Do not run a cycle over 5 weeks! There is no need. Many users of superdrol have reported 15 to 20 pounds of DRY and LEAN muscle gains in the first 3 weeks!!!

This is hands down, to me, the most powerful oral available. Intense strength increases fast. Lean mass build up, fast.
Superdrol and DMZ do not convert to estrogen. No anti E is needed on cycle. Right after though, PCT must start, and be thorough. I recommend Nolvadex.
One could run HCG during the short cycle, and rebound fast, really fast. You will experience faster recovery, due to superdrols DHT like structure and its inability to convert to estrogen. If you follow PCT correctly you could work many small cycles in a year.

One could also add IGf 1 Lr3 to this cycle and have a completely LEGAL CYCLE! (As long as you are using DMZ)

Original article by Dean Destructo
 
That’s something that confuses me Is all the different things I’ve read. I heard people saying it was so toxic it should not be ran at all and it’s worse than halo
 
Dieselmatt said:
That’s something that confuses me Is all the different things I’ve read. I heard people saying it was so toxic it should not be ran at all and it’s worse than halo
Click to expand...

It is not the base compound that make it hepatotoxic. Any 17aa compound is hepatotoxic. I have ran superdrol. I have seen a lot of logs on superdrol. Under 40mgs for 4 weeks is fine, and you will gain a lean 15lbs if you eat right.
 
Halotestin is a modified version of methyltest. There is an extra flouro group at the carbon 9 and 3, and a hydroxl on 11. Highly modified compound. That on top of having a methyl group on the 17th carbon position (17aa methyl).
 
I forgot to add that you could stack or bridge with a SARM. I will look to updating on that premise.

- - - Updated - - -

Dieselmatt said:
That’s something that confuses me Is all the different things I’ve read. I heard people saying it was so toxic it should not be ran at all and it’s worse than halo
Click to expand...

Halo is 17aa. Halo also offers no real world anabolism. It is more of an extreme strength compound IIRC.
 
You have to learn what works for you. What may not work for someone may be a home run for you. Just be safe no matter what you do.
 
Dean Destructo said:
It is not the base compound that make it hepatotoxic. Any 17aa compound is hepatotoxic. I have ran superdrol. I have seen a lot of logs on superdrol. Under 40mgs for 4 weeks is fine, and you will gain a lean 15lbs if you eat right.
Click to expand...
It's the conversion in liver to something else reason Anavar is 17aa and not toxic.
I will bump a thread.

Superdrol 10-15 mg a day helps me alot but 3-4 weeks tops. BUT I recover quick.
M-sten too

Sent from my SAMSUNG-SM-G890A using Tapatalk
 
I posted article on this brother

With 17-alpha alkylated steroids, this conversion from a 17-hydroxy to a 17-keto steroid is prevented. This is key, and if you remember anything from this article, remember the next few sentences. The main difference between 17-aa's and regular steroids is that one retains a free 17 hydroxyl group and one does not, when going through the liver. The reason that 17-aa are toxic is because the free hydroxyl is able to be conjugated with glucuronic acid, forming a D ring 17-glucuronide. It is not the 17-aa steroid that is liver toxic but rather its 17-glucuronide metabolite. So it's not that these steroids are harder to metabolize, but rather the way they are metabolized causes them to be toxic.
Dean Destructo said:
It is not the base compound that make it hepatotoxic. Any 17aa compound is hepatotoxic. I have ran superdrol. I have seen a lot of logs on superdrol. Under 40mgs for 4 weeks is fine, and you will gain a lean 15lbs if you eat right.
Click to expand...

Sent from my SAMSUNG-SM-G890A using Tapatalk
 
@DeanDestructo
I know what u meant and u gave best understandable answer.
I just thought of article I had found and thought let me bump it to further let others understand. About 17aa and what problems are..



Sent from my SAMSUNG-SM-G890A using Tapatalk
 
Muscle mechanic said:
I posted article on this brother

With 17-alpha alkylated steroids, this conversion from a 17-hydroxy to a 17-keto steroid is prevented. This is key, and if you remember anything from this article, remember the next few sentences. The main difference between 17-aa's and regular steroids is that one retains a free 17 hydroxyl group and one does not, when going through the liver. The reason that 17-aa are toxic is because the free hydroxyl is able to be conjugated with glucuronic acid, forming a D ring 17-glucuronide. It is not the 17-aa steroid that is liver toxic but rather its 17-glucuronide metabolite. So it's not that these steroids are harder to metabolize, but rather the way they are metabolized causes them to be toxic.


Sent from my SAMSUNG-SM-G890A using Tapatalk
Click to expand...

The study seems theoretical though. Unless I can see some resources where they studied the conversion in vitro. That is the crazy thing, with out biopsy we can only look for symptoms of liver issues. Which doesn't show us how the problem itself forms. Great article post though! I hope I am not sounding negative lol.
 
Dean Destructo said:
The study seems theoretical though. Unless I can see some resources where they studied the conversion in vitro. That is the crazy thing, with out biopsy we can only look for symptoms of liver issues. Which doesn't show us how the problem itself forms. Great article post though! I hope I am not sounding negative lol.
Click to expand...

Essentially they are hepatotoxic because they are steroids AND 17aa. If we are following the logic of the article you posted then anything that helps with free radicals can treat hepatoxicity, because it clears free radicals. I am researching it more now.
 
I remember i had to cut my superdrol dosage from 20mg down to 10 and in the first week i think it was, cant remember exactly but it was fast and i posted about it back then , as i could believe how quick it worked, but it made me feel shitty at 20mg and man did i blow the fuck up.
 
Presser said:
I remember i had to cut my superdrol dosage from 20mg down to 10 and in the first week i think it was, cant remember exactly but it was fast and i posted about it back then , as i could believe how quick it worked, but it made me feel shitty at 20mg and man did i blow the fuck up.
Click to expand...
I may look into Dmz or superdrol in the future after I run anadrol
 
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