Hi, Lonely. I am kind of hoping the same thing, but other tryptamines with the same chain are not all psycho active. I will try it.no but I would think it would be much like 4 ACO DMT to be honest.
I don think changing the acid moiety on the phenol makes as much difference as the chains on the amine.
If there is any way to break the O benzoyl or 4 ACO into psilocybin, could you point me to it?I have been offered this: O-Benzyl Psilocin CAS 28383-23-5. I have never heard of it and ask if what anyone knows about it, particularly how does it compare with psilocybin family or 4 ACO DMT CAS 92292-84-7 .
This one should be inactive by itself... and not a prodrug for psilocin.O-Benzyl Psilocin CAS 28383-23-5
Unfortunately, this somewhat obscure reference is for the N-benzyl psilocin, whereas OP has been offered O-benzyl psilocin. There is no reason to assume that they have similar activities.its active.
" 1-Benzylpsilocin
No, a "benzoyl moeity" is removed by hydrolysis, just like the acetate or phosphate group of psilocybin and 4-AcO-DMT, these are potential pro-drugs for psilocin.to remove the benzoyl moeity you will have to reduce it off.
I would be surpsised if this rather bulky ester can still fit nicely into the 5-HT2A receptor...but psilocin benzoate ?
Quimchin, I said that... .how does it compare with
I have to admit that I was wrong, sorry. I found that the 4-O-Bn-DMT ether displays h5-HT2A agonist effects comparable to psilocin as reported by Kargbo 2021; DOI: 10.1021/acsmedchemlett.1c00467This one should be inactive by itself...