All I see is "PCP"........ lol. Interesting, I know quite a few will be watching this.
That's PCPr... Pr being short for Propyl, so it's a chain, not a ring like in PCP.
In other words they were going for structural similarities to Ketamine and MXE.
No that's PCPy unfortunately! It was said to have barbiturate like sedation. Sounds very nice but r was stimulating.No, not ketamine. The halogen is in 3 position on the phenyl ring, and not on the 2 position like in ketamine. Considering NENK there's a strong indication that the latter would be inactive. The only structural similarity of this one to ketamine is the 2-oxo, so this one will probably be more a MXE or O-PCE type dissociative - if it's any good at all. I think PCPr was supposed to be more sedative than PCP and PCE.
No that's PCPy unfortunately! It was said to have barbiturate like sedation. Sounds very nice but r was stimulating.
I will get some soon, i will report when i have tested it
Actually 3-MeO-PCPr was commercially available for a brief period of time alongside 3-MeO-PCPy and the first batch of 3-MeO-PCE from the UK. This was in 2011, I think.. 3-MeO-PCPr was indeed almost indistinguishable from it's N-Ethyl counterpart in it's qualitative effects as well as the dosage needed.. If memory serves me right 25mg lead to a smooth +++.. Anyways I am excited how 3-Fluoro-2'-Oxo-PCPr will turn out...It's the first PCPr analogue in possibly decades, however I doubt that N-propyl will be very different compared to N-ethyl in both potency and effects, should be quite close.
so 3-meo-pcpr was around 25mg.... ok, it seems the alkyl-substitute connected to the amine leads to different potency and duration- methoxMetamine needed twice the dosage of MXE. I was thinking, an propyl substituent is going the other way and even enforces the potency. On the phenyl-ring is in position 3 a fluor. This is clearly different from methoxy-groups, fluor is more like an ordinary bound hydrogen with stronger resistance for metabolic oxidation. And even the oxo-group plays an important role i think, it enhances serotonergic effects, while no oxo on the cyclohexane and a methoxy on the phenyl-ring is more responsible for an opioid effect. Removing the halogen (chlor) from ketamine leads to more lucid effects, and even an significant increase in potency. This can be seen on O-PCM. I think with a fluor floxy will be overall between Ketamine and O-PCE within its effects and dosage. Well, this are my thoughts about structure-effect-relationships, i will know more in around an hour :D I will keep you updated
€: i insufflated 5mg...it burns a lot, holy shit :D hydrochlorides are well known for that..... it reminds me of good old 2C-E nose pain oO next time oral is the way to go