08-08-01 21:55
No 202724
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?
(Hive Bee)
08-09-01 01:08
No 202738
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!!!
amines to an end
(Hive Addict)
08-09-01 04:16
No 202753
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
(Hive Bee)
08-09-01 05:54
No 202769
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
(Moderator)
08-09-01 07:28
No 202791
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/stor