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Author Topic: N,N dimethyltrytOPHAN  (Read 3329 times)

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psycosmo

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N,N dimethyltrytOPHAN
« on: August 08, 2001, 09:55:00 PM »
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?
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indole

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Re: N,N dimethyltrytOPHAN
« Reply #1 on: August 09, 2001, 01:08:00 AM »
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.
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amines to an end
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foxy2

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Re: N,N dimethyltrytOPHAN
« Reply #2 on: August 09, 2001, 04:16:00 AM »
Really?

Wow that makes anything that comes from tryptophan decarboxylation suspect.  Scary!!!
Would dipropyl tryptophan have the same effect?

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indole

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Re: N,N dimethyltrytOPHAN
« Reply #3 on: August 09, 2001, 05:54:00 AM »
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
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Lilienthal

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Re: N,N dimethyltrytOPHAN
« Reply #4 on: August 09, 2001, 07:28:00 AM »
It wouldn't decarboxylate on it's own. But possibly while smoking... Check my page for references about its synthesis.

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