Nope. It depends on the position of the 17a, like epistane is the 3rd position, superdrol is the 2nd.
Nope. It depends on the position of the 17a, like epistane is the 3rd position, superdrol is the 2nd. Also look for "dimethyl". That is methylated x2. Someone else should be able to chime in with more information. It's is a good idea to be cautious when staking methyls. Tudca is the best otc protection available, stay off of the booze, drink a lot of water
Um, no. It's 17-alpha alkylation or 17-alpha methylation due to it being attached to the 17th carbon atom. Compounds are more or less toxic based on it's resistance to hepatic breakdown, well mostly. 17-AA tends to be less toxic in general terms compared to 17-AM.
So compounds like halo and epi are 17-AA while compounds like SD/msten are 17-AM?
I feel like there's a lot of heresay going on right now with no real knowledge.
Did a little googling and couldn't find very much on what actually makes each compound more toxic to the liver than another. If they're 17a, then the toxicity should be the same, Mg vs Mg, right?
Huh?
You're correct, all the 17 attachments are alkyl groups. They are either methyl to ethyl derivitives.
So compounds like halo and epi are 17-AA while compounds like SD/msten are 17-AM?
Nope