I guess it would stop being orally active.oxandrolone without the 17-alpha alkylation
Anyone know if this was ever tested / found to be any good?
^^I think I've read of a dimethyltrienolone as a designer steroid. And thanks for the ester clarification. I was thinking of the eq-dbol relationship as well. whyarewenotfundingthis.jpg
I'd like to see the nonmethyl version of oxandrolone made. I wonder how much the properties would change. If we're lucky and they don't change much, you'd have a great compound.
.........Ok, first, thank you both for the reply.
Yeah, found quite a lot about MENT, so no more questions about that. And what he said is about the same as I found on my own.
Is he sure that dimethyl tren and mibolerone are the same thing?
This is tren:
This is methyltren:
This is mibolerone:
Isn't mibolerone missing some two double bonds to be dimethyl tren?
As to why the 7a methyl does what it does good question.
If I'm reading this correctly 7a-methyltren hasn't been tested as far as he is aware, right?
And regarding the oxandrolone without the 17aa anything about that?
......
7a-methyltren, what I'd like to see tested
.............The first 'designer steroid' was THG
which was discovered by Patrick Arnold at BALCO. Synthesis is via hydrogenation of gestinone.
Only a few years later, The Greek olympic weightlifting team were caught using R1881
You can see how similar they are (1 methyl).
I'm not well up on the situation with anabolic steroids, but are people still producing newer and newer analogues?