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Would boldenone w/out an ester attached be orally active w/out a methyl group at 17a.?
I was wondering because Patrick Arnold is stating that his 1-AD is orally active w/out 17aa because it has a double bond at the "top" of the "A" ring similar to primobolan.
Boldenone and it's 17aa brother dianabol both have 2 double bonds in the "A" ring.
Do you think this would make boldenone orally active??
I was wondering because Patrick Arnold is stating that his 1-AD is orally active w/out 17aa because it has a double bond at the "top" of the "A" ring similar to primobolan.
Boldenone and it's 17aa brother dianabol both have 2 double bonds in the "A" ring.
Do you think this would make boldenone orally active??
