Nortilidine is an opioid drug, in the form of a solution, the main metabolite of tilidine, or rather it is formed from tilidine, by demethylation in the liver. The (1S,2R) isomer is an NMDA antagonist and acts as a dopamine reuptake inhibitor. It has excellent analgesic properties, equivalent in potency to morphine, opioid effects are similar to morphine. This drug is actively used in the treatment of pain in the EU countries.
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Description
(1R,2S)-nortilidine is an ethyl 2-(methylamino)-1-phenylcyclohex-3-ene-1-carboxylate that is ent-dextilidine in which one of the methyl groups attached to the nitrogen is replaced by hydrogen. ent-Dextilidine is metabolised to (1R,2S)-nortilidine by the liver. It has a role as a drug metabolite and a NMDA receptor antagonist. It is an enantiomer of a (1S,2R)-nortilidine.
Brorphine is one of the newest designer drugs in the opioid class. Brorphine might be a potent agonist at the μ-opioid receptor, about 8 times stronger than morphine and a potent analgesic. Brorphine currently has legal stsus in many countries and passes customs without any problems.
Oxycodone -d3 designer drug, opiate alkaloid synthesized from tebaine, has a strong effect of an opioid analgesic. You can buy oxycodone on our website as a powder. Oxycodone -d3 is produced in modern laboratory by professionals, in compliance with all standards, which makes it as clean as possible.
2-methyl-ap-237 is a new research chemical, classifying the analgesic opioid. 2-methyl-ap-237 is used in Southeast Asia as a powerful analgesic, with a variety of disorders. It has legal status in many countries. 2-methyl-ap-237 is very similar in action to morphine but is several times superior in potency, unlike morphine, they are strong and selective agonists of the μ-opioid receptor-MOR with a relatively low affinity for the δ-opioid receptor and κ-opioid receptor.
