Fluonitazene is a new opioid analgesic that is homologous to Clonitazene and has a similar effect. Fluonitazene is several times more potent than morphine. Fluonitazene might be a potent agonist at μ-opioid receptor. This drug has excellent analgesic properties, is an excellent hypnotic and relaxant, causes euphoria, but if the dosage is exceeded, it can cause respiratory depression and vomiting.
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(+)-O-Desmethyl-N,N-bisdesmethyl Tramadol opioid drug, analgesic of the Tramadol family, active metabolite of Tramadol in the form of hydrochloride, soluble in Chloroform, Ethyl Acetate, Methanol. (+)-O-Desmethyl-N,N-bisdesmethyl Tramadol has a higher affinity for the Mu-Opioid receptor than tramadol, and has stronger analgesic properties, ((+) -) – both enantiomers inhibit serotonin and norepinephrine.
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Butonitazene is an analgesic opioid of the benzimidazole opioid class, a designer variety of etonitazine analogs. Butonitazene is tens of times superior to morphine when administered intravenously, as was found in chemical studies in rodents. Butonitazene acts as a powerful analgesic, hypnotic, and sedative. Vomiting and respiratory depression may occur at high doses of Butonitazene. You can only buy Butonitazene online as a designer drug for chemical research.
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Etonitazene is an opioid analgesic, first synthesized in the 50s of the last century. Etonitazene has a strong opiate potential, approximately 60 times stronger than morphine. It is a type of benzimidazole opioid, structurally associated with clonitazene (p-ethoxybenzyl group is replaced by p-chlorobenzyl group). With caution in chemical studies in rodents, since at a high dosage, side effects are possible: respiratory depression, vomiting, death, can be addictive.
