AlsoTapered
Bluelighter
There are 6 isomers if viminol. 4 are inactive, one is an agonist, the other an antagonist. It's because it forces the H: into the agonist conformation. In some certain research, N-n-butyl was tested but N-(S) s-butane will NOT allow the H to enter the antagonist conformation.
I've only ever seen this trick in Viminol but antagonists and mixed agonists are also possible. In a lot of research, the N-n-butylamine example is
used and it would be interesting to see which examples need the (S) s-butylsmine, are agonists, antagonists or don't care.
A fascinating way to make a SAFE product.
I've only ever seen this trick in Viminol but antagonists and mixed agonists are also possible. In a lot of research, the N-n-butylamine example is
used and it would be interesting to see which examples need the (S) s-butylsmine, are agonists, antagonists or don't care.
A fascinating way to make a SAFE product.