do all methylated orals have the same liver toxicity? or does it depend on the compound/amount taken or other things?
no depends on the compound. for example...m-drol has a much higher toxicity than say h-drol or epi/havoc. phera compounds can be high also. and the original M1T was even higher in toxicity than superdrol i believe.
why exactly is it harsher on your liver does anyone know?
oh just why would superdrol be more toxic than say epistane mg to mg?
because m-drol is a steroid. it is just a very harsh compound all around in general. i think it has to do with where the carbon atoms and methylated structures are in the make up but i am not 100% on that
It has to do with the steroids individual affinity for glucuronyl transferase. Glucuronyl transferase converts the steroid to a glucoronide metabolite that's toxic to the liver.