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1-methly group

PIOTREK

Member
this is a quote from big cat's article:

"The low liver-toxicity is accounted for that the bio-availability of methenolone is carried by a 1-methyl-group, which lessens the need for a carrier attachment such as a 17-alpha-akylated group, the main culprit in steroid-related liver afflictions."

my question is, why has this alternate method (1-methly-group modification) not been employed in more drugs/once legal prosteroids?
 
The c17aa attachment seems to make the product stronger.. Proviron is 1-methylated, yet it's merely a weak DHT with high oral availability.. Same with oral Primo, it's 1-methylated, yet it's not highly anabolic.. ;)


This is all just my educated guess, though.. Boldenone becomes fast-acting and stronger once it's methylated in the 17th position (methandrostenolone aka Dianabol), so it makes sense..
 
Mesterolone is 1-methyl-dehydrotestosterone, or Proviron if you're nasty... ;)

1-alpha-methyl-17 betahydroxy-5 alpha-androstan-3one is the longer more geeky name..
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Why hasn't anyone made 1-methyl boldenone? Would it just have the same estrogenic / androgenic character as dianabol? At least you could take if for a longer amount of time without liver toxicity.
 
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