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I Like to Draw Pictures of Random Molecules

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Any evidence for those claims other than "it feels wierd"? Most of these cmpds seem very selective for CB1/2 over other targets, and overstimulation of CB1 can lead to very strange psychotic effects...


This cmpd is also known as QUPIC
 
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I got a bit bored and decided to post a few of my ideas, let me know what your thoughts are:

1253x9x.jpg
 
image_zpsecdd281d.jpg


why hasn't this come about yet? Or any other azetine derivatives of pyrridines?
 
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.
 
What would be the point?

For moronic ideas: how about the nitrate ester of ephedrine?

It'll counter the increased blood pressure :)

or explode ;)
 
What would be the point?

For moronic ideas: how about the nitrate ester of ephedrine?

It'll counter the increased blood pressure :)

or explode ;)

haha :)

but why stop at one nitro group? trinitro-ephedrine would be fun, who doesn't like drugs with explosive effects ;)
 
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.

How about the last one, any thoughts on it?
 
11iiput.jpg


Was wanting to throw this one out there last time since 3 and 4 meo exist, why not bridge them?
 
hammilton said:
For moronic ideas: how about the nitrate ester of ephedrine?

It'll counter the increased blood pressure

or explode

Let the future of terrorism be explosives concealed as research chemicals. :P

ebola
 
11iiput.jpg


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:
zxppDQr.png


Non-hepatotoxic analogue of amineptine:
ahAQLY5.png


Methylenedioxybenzofuranylpropylaminopentane :) or, MDBPAP!
LZ1BVIX.png
 
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:
zxppDQr.png

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).
 
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).

For some types of activity it certainly seems necessary. For this one, I would wonder if the absence of the pyrole ring would make a huge difference. It might prevent 5ht2a binding, but I'm not 100% sure. I think it might still have SERT affinity though, and might act as a releasing agent. Some cyclohexene ideas have been thrown around before actually, and I think it's a ripe field for discover ;)

I'm not honestly sure how removing the nitrogen would affect it. I would assume it would keep some sort of dopaminergic activity based on the structure of amineptine, but it could be a reuptake inhibitor rather than a releasing agent. Changing the position of the oxygen probably wouldn't change much.

Haha they actually have done that: http://en.wikipedia.org/wiki/Phendimetrazine
Makes it into a prodrug!

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):
rokku6U.png
 
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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):
rokku6U.png

http://en.wikipedia.org/wiki/A-68,930

Check out this interesting fellow, not quite what you were wanting but very interesting IMO.

I am a bit interested in this guy below

http://en.wikipedia.org/wiki/A-77636

I find bromantane is useful and have stumbled on (distantly) related stimulants, the anxiolytic + stimulant combo is very ideal.

As an added bonus I will throw in another interesting dude below:

http://en.wikipedia.org/wiki/SKF-82958

I hope you find these at least mildly interesting, dopamine agonists seem to be extremely variable and have always intrigued me.


Would love to find 'functional' dissociative with mild dopamine release, IMO this would be the perfect everyday boredom buster. Tune out everyone else but your self and your ambitions/duties and have motivation whilst doing so. Maybe throw in some neuroprotective properties for good measure but ehh sometimes we think a bit too much.
 
dingophone, that compound would sooner fall apart than be absorbed by a human cell. Typically the N-CH2-OH motif is pretty... uncommon warranting to its ability to decompose to formaldehyde and an amine.

Aromatic rings are needed for activity at most transporter sites and things like serotonin receptors - the exception tends to be the adrenoreceptors which seem to be pretty promiscuous for alkylamines especially (see, for instance, tuaminoheptane... possibly one of the simplest drugs?). I think NET has a little tolerance for bulky alkyl groups in general, but remember that propylhexidrine (hexahydro-dextro-methamphetamine) is about 1/100 - 1/1000 as potent as the drug it is 'derived' from !

Nobody gets arrested for extracting nasal inhalers to sell on the street, either...

Also, to my knowledge, nobody but rats and monkeys have been trialed on wierd ass D1 full agonists. I can only imagine using such a drug would have an effect somewhat similar to that of a rampaging bull in a china shop on the psychology of most people. A drug with no primary effects - not a stimulant nor a depressant nor a hallucinogen, that just induces reward? Seems like something out of a bad remake of Limitless...
 
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