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Enadoline - psychotomimetic kappa opioid receptor agonist

crOOk

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wiki said:
Enadoline is a drug which acts as a highly selective κ-opioid agonist.
In human studies, it produced visual distortions and feelings of dissociation, reminiscent of the effects of salvinorin A.[1]
It was looked at as a potential analgesic, but abandoned because of the dose-limiting effects of dysphoria, which could be expected from a κ-opioid agonist. There was mention of its potential in treating comatose head injury or stroke victims, where that type of side effect would be immaterial.[2]

[original post:]

Supposedly this is similar to salvinorin A. Found this in a study from 2001:

"Enadoline significantly increased measures of sedation, confusion and dizziness, produced visual distortions and feelings of depersonalization, and increased urinary output. The highest dose (160 microg/70 kg) was not tolerated and led to psychotomimetic effects." (Enadoline, a selective kappa opioid agonist: comparison with butorphanol and hydromorphone in humans, Psychopharmacology (Berl). 2001 Sep;157(2):151-62.)

Has anyone ventured there?
 
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I read that paper you're quoting from, and I don't think it sounds very pleasant, a little too much on the dysphoric side. Of cause, some people might find that sort of thing fun :) It's a fascinating compound none the less.

Psychotomimetic effects of high-dose enadoline

Only two subjects were exposed to the 160-μg/70 kg dose of enadoline and both experienced adverse effects; therefore, it was excluded from further testing.

The first subject reported no history of hallucinogen use, while the second subject reported limited experimentation with hallucinogens 19 years earlier. The two individual responses are described below. Data from these two experimental test sessions were not included in the data analysis. The final data analyses included only the eleven test conditions to which all six participants were exposed.

Participant no. 4
This volunteer received enadoline 160 μg/70 kg during his 11th test session; he had already been exposed to all
of the other doses of enadoline up to 80 μg/70 kg.
Twentyfive minutes after the injection, he reported somatic effects, including the sensation that his body was hot but unable to radiate heat.
Fifty-five minutes after the injection, he reported visual and auditory disturbances (an inability to read words on a computer screen, distortion of staff voices). At 68 minutes after drug administration, he reported visual and tactile hallucinations; these consisted of a “blue wing” that he was able to both see and touch, and he was observed to be moving his hand as if grasping an object. The participant continued to have somatic effects during this time (e.g., itching and chills).
Ninety minutes after drug administration, all abnormal effects had essentially resolved. The participant did not
recall these events after the test session. That evening he watched television with peers, ate without difficulty, and was pleasant and cooperative.

Participant no. 6 This volunteer received enadoline 160 μg during his ninth session; he had already been exposed to all of the other doses of enadoline up to 80 μg/70 kg. Within 10 min after receiving the injection, he reported unusual sensations, including the floor moving and his skin prickling. He became agitated, began swearing, mistrusting others, and accused staff of seeking to harm him. He removed the physiological monitoring leads and left the session area with staff accompanying. His gait was noted to be swaggering and unsteady. Within 2 h, the effect had resolved.

Afterward, the subject reported that he had seen and felt waves, for example, as a part of the floor.
He had felt that his body was blending with these waves. He reported he had felt others were conspiring against him in a desire to ruin his mind.
That evening he was cooperative and pleasant; recalled the earlier events and expressed embarrassment and remorse for his aggressive behavior and foul language.
 
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Within 2 h, the effect had resolved.
Two hours is entirely too long for a salvia-like drug to last. Given that a salvia alternative with a similarly short duration like salvinorin B ethoxymethyl ether hasn't been marketed, I doubt that anybody will have tried this who hasn't had in custom synthesized (and if you're bothering with that, why not go with salvinorin B ethoxymethyl ether?). Somebody offer "Symmetry" already.
 
Of cause, some people might find that sort of thing fun.
Exactly. :D This would be very nice to sample.

I personally always found both salvia plant matter and salvinorin a to last way too short.
 
Sure love the name, though! Maybe this stuff is like 5-MeO-DMT vs MiPT or something....it could be less a conk on the head and more a useable, trip with time to make sense of it all!

Edit: read right over Faggot's comments. Clearly it is a conk on the head.
 
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Sure love the name, though! Maybe this stuff is like 5-MeO-DMT vs MiPT or something....it could be less a conk on the head and more a useable, trip with time to make sense of it all!

Edit: read right over Faggot's comments. Clearly it is a conk on the head.
Well, when I smoked salvia I could definitely never communicate on it AT ALL. I've tried, but I could never actually form words. So considering that the people in these trials are most likely drug naive or at least naive to dissociatives like salvinorin, you might actually be right.
 
It was available from a EU vendor for a while. Haven't seen any reports from people purchasing the material though, so who knows. But it has been marketed at least.
Wow, sounds pretty fucking awesome to me. :D It's pretty impressive how strongly alpha's and beta's reports resemble my first salvia experiences.
 
It was available from a EU vendor for a while. Haven't seen any reports from people purchasing the material though, so who knows. But it has been marketed at least.
Are you sure it wasn't scam? I mean, how would you even go about selling something like that?
 
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