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I Like to Draw Pictures of Random Molecules

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Reduction of Ambien's (zolpidem's) N,N-dimethyl amide functional group to the N,N-dimethylethanamine (I'm not gonna say how, but it isn't hard to figure out) should produce a drug that packs quite a wallop.
 
z7BnngC.png


That should be a banging cannabinoid.
 
8-OH-quinoline (alcohol on the ester there) is a transcription inhibitor/putative cancer chemotherapy drug, I would not like that accumulating, no sir.
 
All in moderation! BB-22 was quite enjoyable. Could always replace it with a naphthalene group (probably not the safest thing ever either though).
 
i went through a gram of BB-22 in a few months. i felt EXTREMELY odd by the end of it. looking back, its actually when a few of my current health problems started.
 
Could be interesting nonetheless! N, N-Di(propyl-1-oxo)-Tryptamine!

If you only managed to ingest it without breaking it down in the process... ;) So it's like it could be interesting if we only lived in a different realm with different rules governing it, but unfortunately we're carbon-based lifeforms with lots of water inside. =D
 
If you only managed to ingest it without breaking it down in the process... ;) So it's like it could be interesting if we only lived in a different realm with different rules governing it, but unfortunately we're carbon-based lifeforms with lots of water inside. =D

injection straight to the cerebellum? =p





8-OH-quinoline (alcohol on the ester there) is a transcription inhibitor/putative cancer chemotherapy drug, I would not like that accumulating, no sir.

All in moderation! BB-22 was quite enjoyable. Could always replace it with a naphthalene group (probably not the safest thing ever either though).

i went through a gram of BB-22 in a few months. i felt EXTREMELY odd by the end of it. looking back, its actually when a few of my current health problems started.

after realizing that, the more i think about it, the more i think that BB-22 kinda messed me up when i smoked it last year. i acquired it at the same time that i got my gram of 3-MeO-PCP, and i was definitely abusing both of them. around that time i started noticing some issues with my bowels, some numbness in my lower extremities, and some odd heavy feelings in my lungs. at the time i attributed all those effects to the 3-MeO-PCP. but this year, i picked up some more 3-MeO-PCP, and didn't notice any of those side effects. i thought that was odd, but figured it was attributable to other changes in my life. but yeah, the more i think about it now.... i think that BB-22 was more of a culprit.

good information, thanks sekio.

BB-22, for reference: (NSFW for size)

NSFW:
BB-22.png
 
I thought of this in the shower the other day. not viable to make but interesting to think about :)

KP94epMm.jpg


ps: doing a fluorobenzyl sub on JWH-122 is really where it's at gaiz
 
Psilocin with aminoindane-like structure.

0Ri44YQ.png

Funny, I had thought of a similar perversion of TMA-6:

TVtvxaZ.png


or, perhaps to stay truer to form:

Y5hSJsR.png


Moving the 5-MeO to 6 doesn't seem to destroy activity and phens seem to respond well to constraint (planarity) so the question in my mind is what a more efficient 4-sub would result in. it's kind of a moot point with indanyl psychedelics like 2CB-Ind, jimscaline & friends waiting to be explored, though

Edit: on the 1st image, per existing indanyls my amide is both too short a chain and in the wrong spot... but you get the idea

almost dragonfly-ish if you look at it

whoa! i wish i had thought of that! looks like a winner!

thanks :)
 
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From I've been taught, you can't have a N and an O sharing the same carbon (or 1 carbon away from each other, to state it differently). As for the other one, it is probably not safe, as 100mg or more of the related 2-aminotetralin will send you to the hospital. Also, I've done TMA-6 and didn't even enjoy it. I would love to try all four "5"-MeO-(5 or 6)-AP(D)B's, though.
 
Do we need a campaign against aminal abuse?
tcgxLY4.png


These guys are hydrolytically and enzymatically unstable, they are valid compounds indeed, but they have a tendency to decompose to ammonia and the parent aldehyde (!)
 
Psilocin with aminoindane-like structure.

0Ri44YQ.png


Huh, that's actually a more interesting compound than I thought. I was looking on the LSD analogue Midnight Sun posted and made a similar connection.

Here's the same molecule on a different angle, plus the piperidine version aside. Looks very LSD like! I wonder if adding a double bond somewhere could help with the activity.

J00A3iP.png
 
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