• N&PD Moderators: Skorpio | someguyontheinternet

I Like to Draw Pictures of Random Molecules

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What makes the amines so important, why don't we get phenethanols or tryptanols(?) ? Somehing to do with it being basic I presume.

Yep! If I remember correctly, the amine have to be protonated to bind to the different serotonin receptors. So it's related to the basicity of the amine...
 
qk69.png


jg4z.png
 
Well, then it would be really unstable and probably too polar too penetrate the BBB well.
 
I believe the first one was in Ralf Heim's thesis, the same one containing RH-34 and 25I-NBOMe. If memory serves me right it is either untested or an antagonist at 5-HT2a, but I will have to double check to be sure. I am close to 100% positive that he did in fact synthesize it though.
 
Molimage


GPCR ligand 0.23
Ion channel modulator 0.30
Kinase inhibitor -0.51
Nuclear receptor ligand -0.18
Protease inhibitor -0.20
Enzyme inhibitor 0.22

miLogP -1.703

or

Molimage

GPCR ligand 0.28
Enzyme inhibitor 0.27
 
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what's going on with the Texas peroxy oxygen with a methyne off of it?

if you fix that up chances are it wil follow the fentanyl SAR. the presence or absence of methylenedioxyphenyl grous is by no means a metric for "is this an empathogen or not".
 
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I let you guys find the name for this

Nay, the molecule will spontaneously decompose to dodecahydroxydodecadehydrocoronene (the core) and 3,4-(2,2-dihydroxymethylenedioxy)phenethylamine.
The latter might then break down to glyoxal too...
 
unlikely. the methylenedioxy group doesn't tolerate much bulk, and chemically a geminal dihydroxy compound like that would decompose to water and 2-keto-MDPEA.
 
Ketamine without the ketone? I can't find anything about it, any one knows anything? it must have been made.
 
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