• Neuroscience & Pharmacology Discussion Welcome Guest
    Posting Rules Bluelight Rules
    Recent Journal Articles Chemistry Mega-Thread
    FREE Chemistry Databases! Self-Education Guide

  • N&PD Moderators: Skorpio | someguyontheinternet

I Like to Draw Pictures of Random Molecules

Status
Not open for further replies.
Yup!

thenightwatch said:
^ indeed

here's an easy one:

______O
_____||
HO\/\/\OH
Click to expand...

GHB (Gamma-Hydroxy-Butyric acid)

Katuskoti said:
^ GABA!!

1 billion points to the first poster that can get this one (hint: very closely related to GABA)
_______O
H2N/\/\//
.____|_|
____/\_OH
.___|_|
____\/

edit: I have no life
_________O
H2N/.\./.\.//
.___._|__.|
.___./_\\_OH
.___|l_._|
.___.\,.//
Click to expand...

Me neither! YAY! That one is phenibut.
Cool. (┌●_●)

Here's another molecule I drew. NZX-18986 (NZX-18,986).
64kujc.png


Here's another one. It's 2C-PH-I.
16ixnxl.png

Here's 2C-Ph.
2i1ihy1.png

Here's 2C-NAP-I
20i6r9s.png
 
Last edited:
^ Ding ding ding! You win! Jesus though. I can't brain today I have the dumb. Amide and hydroxy are totally the same guys. The only difference is one is aromatic and one isn't. So only one is the future of 'smells' that get you high. (jk :D)

Skyblue you should just write Pihkal 2 already! Those are awesome though.

O^i^

<O^i^

_┐
.,O^^
_└
 
2z9m79c.png


what about this one? has it been synth'ed? is it active or doesn't that position take any kind of substituents? since, according to recent literature, the metabolites like HHMA and HMMA are most likely to be the cause of neurotoxicity at high(er) dosis, we could make the molecule a bit less susceptible to attack from those pesky enzymes. if it doesn't work, just replace the methyl by a t-butyl, but i don't think we'd have any chance of seeing activity then ;)
 
I didn't mean to say it would be very active/good just that it may have at least some activity.
 
I came home today and it says that the books were delivered, so I get them Monday. Later than expected (I thought they would come before I left), so about another week until I start drawing molecules.
 
The 2C-Ph-x series might carry high nootropic potential. Based on the activity of 2C-x at sub-psychedelic doses.
2C-Ph-D. Get it? 2C-"PhD"?
293ug7a.png

2C-Ph-I
16ixnxl.jpg

2C-Ph. This molecule alone may carry stimulant effects.
2i1ihy1.jpg

Here's Super E, or Super MDA. Let's call it Jenny-X. %) The theory is that if the 2 oxygens are closer together, it'll become more active and enpathogenic.
xe3le1.png

Here's 2C-Ph-C.
2v1sq47.png

Here's 2C-Ph-T-4.
2l94m6e.png

Here's 2C-Ph-Se-4.
2vajb54.png

This one is 2C-Se-4.
302cenb.png

2C-Fluorenol.
2bwor9.png

Here's AcBZP, or Acetic-Benzylpiperazine. It looks similar to sunifiram, and ione of it's metabolites might be BZP. Other nootropics have a BZP metabolite. Hopefully, the AcBZP has some nootropic potential. I think that if such a molecule were to exist, doses must never exceed 25mg. 8o
2rdalp3.png

There's also more molecules. Stay tuned!
Here's 2C-Sm. The longer name is 2,5-Dimethoxy-4-Sesamylphenethylamine.
2q8bpy0.png

Here's 2C-6MO-I. The longer name is 2,5-Dimethoxy-6-Methoxy-4-Iodophenethylamine.
166j5dt.png

Here's 2C-3MO-I.
2mwtht4.png

Here's 2C-3Mo-6MO-I
25iqc1e.png

Here's 2C-2MD-I. The longer name is 5-Methoxy-2,3-MethyleneDioxy-4-Iodophenethylamine.
jjpag4.png

Here's 2C-5MD-I. The longer name is 2-Methoxy-5,6-MethyleneDioxy-4-Iodophenethylamine.
xpa2dw.png

Here's 2Z-I. The longer name is 2,3-MethyleneDioxy-5,6-MethyleneDioxy-4-Iodophenethylamine.
2yxi1eh.png

The last one, 4Z-I.
120nrl3.png
 
Last edited:
ShaggyFin said:
I came home today and it says that the books were delivered, so I get them Monday. Later than expected (I thought they would come before I left), so about another week until I start drawing molecules.
Click to expand...

Love your videos dude! You're gonna be a well-loved and popular member on this forum! Keep it up!
 
Hold on, aside from the fact that he has no business doing research experiments or anything related... aren't hops supposed to have a sedative effect? I do wonder what is actually known about the (albeit mild) psychoactivity.

Likewise I'm curious about theanine and how other alkylamide homologues besides the ethyl compare. Unfortunately the MOA seems to remain obscure.

theanine_analogues.jpg
 
Status
Not open for further replies.
Top