But the pharmacology of classical psychedelics and MDMA is quite different, which I'm sure you know... one is a releaser and one is a receptor ligand. Of course their effects on the body are going to be quite different, and their metabolites are going to be different as well. I don't claim to know much about malignant hyperthermia but it seems a bit useless to say that because both act on the same receptors, it is odd that they have differing side effects.
While I do admit that both the 2nd and 3rd example were unfitting and unneeded (the latter being caused by a a misconception about the effects of MDMA), I wonder why you keep attacking me on a level like that. It's gonna leaed nowhere...
I replied to your statement "the psychedelic experience is generally very similar in effect within classes" (which followed the not-so-subtle insult) and simply tried to name examples where this is not the case. The first one being dmt and mescaline (or psilocin to come structurally as close as possible) and that one was sufficient to show that the experience can be vastly different despite a very similar structure and being considered to be in the same class. Further examples would be DPT and AMT or DiPT and 5-MeO-DMT. They all share common traits, but can't really be compared when it comes to their impact on the mind.
Regarding the mescaline hcl, I was referring to hcl salts of an alkaloid mix obtained by performing an a/b extraction on dried cactus plant matter. I apologize sincerely for having suggested I'd know anything about what you enjoy and don't enjoy. Oh and btw, alkaloid extract and plant matter are a whole different ballgame and I've personally never managed to ingest enough cactus to get to where the alkaloid salts alone take me and even if I did, the slow absorption can cause the trip to build up over 4h before reaching a plateau which is not comparable to seeing your puke sparkle like a see of diamonds within 15minutes after ingesting the drug. Oh right, you don't really think the difference is worth talking about and even mentioning that it might take you anywhere you haven't been yet seems to trigger a defense response.
It should also be noted, though, that there are many subtypes of 5-hydroxytryptamine receptors which account for many different types of hallucinations and sensation (which is why I suggested organic chemistry). These mechanisms are the root source of the psychedelic experience.
Relating all this to the topic, many people will take you much more seriously if you really understand what is happening in your body, and can show them that it is legitimately not unhealthy, and even good for you.
So I joked "Mescaline is good for you because it's natural" which you then took as reason to insult me by telling me to learn basic biochemistry. Now you're holding onto that cheap shit by implying that neither are people taking me seriously, nor do I know what is going on in my body.
I'm sorry if you think so because this way neither of us will learn anything from one another. I actually consider myself to have pretty good knowledge of the human body overall, but it's not easy to remember everything from the anatomy of the toes over the developement of the teeth to the effects mdma has on your body. Kudos if you can, but with calling such exceptional talents your own it seems hardly fair to expect the same from me.
Therefore a suggestion: Before pointing out what you consider a false statement in the form of a plump insult, why not educate other people with the correct version instead? I personally would love to hear your version of how different psychedelic experiences relate to different 5HTr's... That being said, I do not consider psychedelics "good" as a whole. They have some medical uses (few though) and I personally have enjoyed them immensely and extensively, but I would most definitely rather consider them a threat to a person's health before I claim they're "legitimately not unhealthy", especially not when considering the fact that some of these chemicals you two are referring to (DOC and 2C-E) have never seen any clinical trials sufficient to determin a safety profile.
Aside from that, the problem was the being taken TOO seriously instead of not seriously enough.