We have been working with ketoxime functions in place of 3 position ketones. Initially in effort to crease a different version of a prohormone then the usual diol or diones with the thought that the ketoxime should hydrolize within the body to a ketone. This was first ketoxime compound was "The One" by AppNut which was Mestanolone(17a Methyl DHT) with a ketoxime function in it's three position, this compound was later cloned by CEL and released as D-Plex.
These compounds have both been discontinued for several years now and no one else has attempted a ketoxime compound.
Since it is extremely difficult to get pure M1,4ADD(ph to Dbol) we asked out chemists if they could produce a dbol with a ketoxime function vs a diol and they said yes, and it turned out more stable and we then had Dianodrol. Soon after BA decided Proviron is a hell of a drug, and they did the same to it, releasing Mestebol.
Now the interesting factor is when we added the Ketoxime function group it changes the whole effect of the steroid, it turned out dry unlike dbol which is wet. This leads us to believe that the ketoxime function may not be cleaving and just interacting with the AR by itself. It was hard to distinguish this with The One/D-plex because you already had a dry steroid so you would only assume it is converting. It's not overly far fetched we've seen that the 3 ketone function isn't overly important in AR binding or agonization(see Phera, Epi, Proto, Mithras, Triumphalis).
So in an effort to get a compound closer to the effects of M1T then M1A we are making a M1T with a 3 ketoxime function.