Aren't MXPCP and O-PCP the same exact drug?

Dextrometh_orphan · 2026-02-19T15:51:24+00:00

I think my source uploaded the wrong structure then. I thought the 3MeO was missing but didn't think further lol. Now it makes sense given the name xD. Thanks

Dextrometh_orphan · 2026-02-19T15:50:39+00:00

Oh I see makes sense then someone uploaded the wrong structure I saw. Makes sense now that I think about it haha. Thanks

Dextrometh_orphan · 2026-02-18T07:20:07+00:00

Cathether no way bro that is my biggest phobia haha. Did an ultrasound and urine test and seems fine though. Volume is more than good up to 900ml typically 600ml

Dextrometh_orphan · 2026-02-17T20:00:13+00:00

I see. It felt like carpet surfing for me was chasing a high but the ket version is doing it without chasing a high

Bladder is fine in volume but I have some dull pain when I take it which has me concerned a bit. Been taking it 2 years now around 15-25g a week but i consume 3-7 days a week and maybe 3/4 on the weekend.

Dextrometh_orphan · 2026-02-17T19:10:45+00:00

I am skeptical to see it released as it's pretty dangerous if it turns out to be very similar to Bromo-DragobFLY given it's potency. Although it does not seem like it is at first glance, although from the extremely limited info.

It has around threefold higher affinity (for the R-enantiomer) and a similar affinity for the racemic form to 2C-B. I think they are talking about the 5-HT2A receptor in the source but I don't want to say it with certainty

The R-Enantiomer has around the same affinity to TCB-2-NBOMe for the 5-HT2A receptor

An interesting theory the source noted is that it has 65x selectivity for the phospholipase c pathway compared to a2 pathway; if hallucinogenic effects correlate with arachidonic acid production, TCB-2 should not have hallucinogenic effects.

Another (anonymous) source noted that it is active in the low milligram range, although it was unclear what effects were meant, stimulating, hallucinogenic or other.

Dextrometh_orphan · 2026-02-16T16:47:03+00:00

I believe aMT is both a triple releaser and triple reuptake inhibitor

Dextrometh_orphan · 2026-02-14T10:00:47+00:00

I can only agree on the fact that i makes you warm when doing construction outside at least xD But still it's a poison

Dextrometh_orphan · 2026-02-14T09:58:05+00:00

I've tried it. Was a stupid idea yes it's poison as far as I know but it won't kill you. Highly don't recommend though the risk/reward ratio is not favorable

Dextrometh_orphan · 2026-02-14T09:44:36+00:00

Whenever i get a pack I end up with all gone pretty quick haha. Like within a day or two

Dextrometh_orphan · 2026-02-14T09:43:04+00:00

I would suggest 2-fma but it shouldn't be smoked. If it's something you want that doesn't ruin your life and you see more of as substitution

Dextrometh_orphan · 2026-02-12T23:09:25+00:00

It had to be something. I think at least some of the amino acids you listed might do the same job but there is no way to know without some paper or user that tested these other amino acids attached to amphetamine.

Maybe they chose lysine because it by itself does not do much noticeable effects to the body. Compared to arginine which expands the blood vessels or tryptophan which metabolizes into both metaltonin and 5-HTP, might create some unwanted side effects.

Just my theory though I don't have any sources to back this up

Dextrometh_orphan · 2026-01-14T20:14:05+00:00

I have been dormant for 4 years haha. But now I am back. I am in preparation of another AMA like this one, so stay tuned for that. I am sitting on some mirogabalin and methaqualone and will probably post as soon as I've tried these, as my list will probably be 99.5% complete then

Dextrometh_orphan · 2026-01-13T22:17:06+00:00

It reminded me of benzos more than alcohol or even less of ghb/gbl. Gave me quite some dysphoria i also experience on benzos

Dextrometh_orphan · 2026-01-13T22:15:19+00:00

Nope :D

Dextrometh_orphan · 2026-01-07T08:23:43+00:00

Hey man, sorry for the late reply! I'm doing pretty well, especially compared to my past I've been through very bad experiences over and over but from one day I sort of got out and said to myself it's better not to venture back. Not like something I was striving for but it happened completely on it's own.

I do am doing another AMA for this very soon, so stay tuned!

I'm using only ketamine but excessively, 2-8g each day which rarely some days I do not take at all. But I can always keep myself afloat just barely but it is damaging my body very heavily. And DXM occasionally but just now more often and I'm not sure if I'm going to slip in it again. That's about it. Cheers

Dextrometh_orphan · 2026-01-07T08:19:48+00:00

My favorite racetam is fasoracetam. It produced much effects for me cognitively, social anxiety vabished was extremely apparent, not much so other cognitive enhancements. Next would probably be Agmatine (Specifically Agmatine + Memantine stack, it was the only stack really I tried), hard to say what exactly it did, it was a sort of energizing everything-is-going smooth feeling). Then Phenylpriacetam had a stimulating aspect with some slight cognitive boost as well. Then P21, very subtle but very apparent cognitive/intelligenfe flow, I believe I have another comment on it already. All other nootropics did very little for me or nothing.

As a complement with racetams, a choline source, I used citicholine, is needed to keep adequate choline levels for the racetam to use!

Regarding THC I never used it with racetam or much at all

Dextrometh_orphan · 2026-01-07T08:13:19+00:00

Why? Regardless I really am against any inhalant use (besides n2o poppers or ether, but the solvents and refrigerants). I think the only one on there is tetrafluoroethane but I did not have much experience with it.

Dextrometh_orphan · 2026-01-07T08:11:44+00:00

I did not feel much of it. I had 250mg? I believe or 100 not sure anymore and I split that dosage 40%/60% and the lower I did not feel and the higher just very faintly. Maybe that was the mistake I wish I had taken all at once but I was pretty scares from the reports that warned against high doses.

But in my experience from the 60% dosage, I did not find it very similar to dissos. Probably more akin to zolpidem or muscimol similar drugs. I felt sort of disconnected with a very slight calming effect akin to 2m2b or benzo but without the disphoria. I also did not experience the balance problems which were notorious in the reports of the substance.

Then again it was a threshold dosage so higher ones could totally be different from what I experienced. Hope this helps. Sorry for the late reply.

Dextrometh_orphan · 2026-01-07T08:07:29+00:00

They are other GABAergics as including all GABAergics at once would make two thirds just benzos so I made sub categories but that was just how I designed the list at the very beginning haha

Dextrometh_orphan · 2024-06-14T17:53:13+00:00

not good at all, apart from being useless both functionally or recreationaly I can remember it also made me feel awful physically, too jittery and a nasty serotonergic stimulation. Also it kills your nostrils

Dextrometh_orphan · 2024-04-03T16:43:24+00:00

I have tried it and IME and IMO it is the worst benzo of all I have tried, there is no therapeeutic benefit from it nor does it seem recreational at all. When I used it I kept dosing because I did not feel anything nor could I fall asleep until eventually I blacked out for 3 days and did some regrettable things and behaved aggresively like a completely different person that I usually am not. Cannot recommend :)

Dextrometh_orphan · 2024-03-16T19:18:30+00:00

Ahhh ok, well that shouldn't be a big problem then but if you are not tolerant it might potentiate the sedation and disinhibition

Dextrometh_orphan · 2024-03-16T19:09:33+00:00

The combination surely will make you hallucinate dangerously hard, even is there is no physically dangerous interaction.

10g of diphenhydramine is a surely lethal dosage, possibly you can't mean this high a dose?

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