N&PD Moderators: Skorpio | someguyontheinternet
What happens if you add an acetyl group to the beta position on phenethylamines?
then you'd get ephedrine and acetic acid because it's quickly cleaved by esterases.
What would be the point?
For moronic ideas: how about the nitrate ester of ephedrine?
It'll counter the increased blood pressure
or explode![]()
azetine rings are rather hard to construct.
also, blowjay, many of those compounds are hemiaminals, ketals, or lactones, so they wouldn't be very stable.
hammilton said:For moronic ideas: how about the nitrate ester of ephedrine?
It'll counter the increased blood pressure
or explode
That's super cool, 3,4-MDPCP?![]()
Was wanting to throw this one out there last time since 3 and 4 meo exist, why not bridge them?
That's super cool, 3,4-MDPCP?I'd like to see the pharmacology of that one haha.
Here's some things I've come up with recently.
DMAA-based tryptamine analogue:
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I liked this one, have always been interested in DMAA having activity, makes me wonder how much of a ring system is really needed for some recreational activity, propylhexedrine always intrigued me, what would a cyclohexene ring do instead and what about placement of double bond?
I am wondering about analogs of Phenmetrazine as well, why not move the oxygen over one closer to the nitrogen and see what that does of why not just replace said oxygen with a carbon instead?
http://www.chemspider.com/Chemical-Structure.14447455.html
Hell, why not methylate the nitrogen while we are at it?
Someone entertain my ideas, always wanting to 'learn' (or at least ask questions).
Also, here's something else I made hoping to find a dopamine agonist/reuptake inhibitor and GABA transanimase/reuptake inhibitor (based on dopamine and bamaluzole/muscimol):
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