• N&PD Moderators: Skorpio | someguyontheinternet

Drug designs. (MedicinalUser SAR thread)

Just having a phenol/thiol group on the aromatic ring is likely to be too polar. For this reason they normally occur as the methyl ethers.
 
Here's the other version of MDMA-K that I didn't post. You see when you add the extra methyl it weakens the bioactivity of the structure. Making it target less of the A-G coupled protein receptors. https://ibb.co/QbzJxB2
 
Imagine the sodium salt of a C-2 sulphur substituted version of vinylbital. I bet that one would knock arse right over. There is actually a thiobarbiturate version of Seconal and Nembutal, so having one of Optanox would be interesting. Strangely enough I've never seen a thiobarbiturate version of Amytal, which makes me wonder what happened there. My guess is likely because they already had Surital and that having one anaesthetic barbiturate in their respective market was enough for them.
 
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