Has such a thing ever been produced? Would it decarboxylate in vivo to DMT? How hard would it be to synthesize? Would it be considered an analogue?
Check TIHKAL, I seem to remember N,N-dimethyl-tryptophan as being fatal in humans at 1 mg. This would be in the section of TIHKAL where Shulgin talks about biosynthetics.
DON'T INGEST YET!!! :P
amines to an end
Really?
Wow that makes anything that comes from tryptophan decarboxylation suspect. Scary!!!
Would dipropyl tryptophan have the same effect?
Do Your Part To Win The War
Or maybe I have been up too long...
I am looking at the book now and see a section where it talks about extracting tryptophans from plants and talks about a seed containing mono and tri n-methyltryptophans that contained an extremely toxic protien fragment...
so i was probably wrong, but it is wise to do some research first... ::)
amines to an end
It wouldn't decarboxylate on it's own. But possibly while smoking... Check my page for references about its synthesis.
http://www.fortunecity.com/westwood/storey/116 (http://www.fortunecity.com/westwood/storey/116)