huh...an ester form of stanozolol isstead of a 17 alpha methyl...huh....does not sound to bad powder guy..kinetics might be bad due to poor shbg binding. dose would have to be adjusted to maintain therapuetic levels. the last thing i want to see is cumulative toxicity, so kinetics would be a MUST.
you kind of lost me on the "1 androstene 19 nor ethyl testosterone) what carbon are you saying to put the ethyl? by itself a 1-ene on an estrane analog(19-nor) is not as stable as it would be on a androstane(the methly group would increase stability of the 1-ene on an androstane through carbocation stability and steric hindrance) just a theory. i base this science on totally nothing. if i was going to make an estrane with a 1-ene stable i would add a 4-ene and maybe a 4 chloro group added(dont forget the 17 alpha methyl( nor-clostebol (bingo)........but illegal, stupid president bush