Синтез jwh 09

Синтез jwh 09

Синтез jwh 09

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Наркотик дживиаш (JWH) - что это такое?

Синтез jwh 09

Отзывы о карбамазепине

JWH , a synthetic cannabinoid , is an analgesic chemical from the naphthoylindole family that acts as a partial agonist at both the CB 1 and CB 2 cannabinoid receptors. It is somewhat selective for the CB 1 subtype, with affinity at this subtype approximately 5x the affinity at CB 2. Huffman , one of the inventors of the compound. On 20 April , JWH was claimed by researchers at the University of Freiburg to have been found in a 'fertiliser' product called 'Forest Humus', along with another synthetic cannabinoid C8 - CP 47, As a full agonist at both the CB 1 and CB 2 cannabinoid receptors, this chemical compound is classified as an analgesic medication. The analgesic effects of cannabinoid ligands, mediated by CB1 receptors are well established in treatment of neuropathic pain, as well as cancer pain and arthritis. As the cause is poorly understood in chronic pain states, more research and development must be done before we can realize the therapeutic potential of this class of biologic compounds. Its effects are produced by binding and acting as an agonist to the CB 1 and CB 2 cannabinoid receptors. The CB 1 receptor is found in the brain. JWH bind to CB 1 with a higher affinity than THC, suggesting that taking more too soon after the initial dose could lead to diminished effects. CB 2 is found outside the brain, mostly in the immune system. A search in the literature yielded no published studies of the effects of JWH in humans, but these studies in animals suggest with high probability that JWH produces effects very similar to those of THC in humans. From Wikipedia, the free encyclopedia. Chemical compound. IUPAC name. Interactive image. See also: JWH August Drug Alcohol Depend. July Forensic Science International. Archived from the original on August 3, Retrieved August 5, Retrieved 11 March Archived from the original PDF on June 4, Retrieved August 2, Archived from the original on Retrieved WIN 55, Diphenidine Ephenidine Fluorolintane Methoxphenidine. Dextrallorphan Dextromethorphan Dextrorphan Racemethorphan Racemorphan. Apomorphine Aporphine Bromocriptine Cabergoline Lisuride Memantine Nuciferine Pergolide Phenethylamine Piribedil Pramipexole Ropinirole Rotigotine Salvinorin A Also indirect D 2 agonists, such as dopamine reuptake inhibitors cocaine , methylphenidate , releasing agents amphetamine , methamphetamine , and precursors levodopa. Glaucine Isoaminile Noscapine Pukateine. Cannabinoid receptor modulators. Agonists: Revosimeline. Namespaces Article Talk. Views Read Edit View history. By using this site, you agree to the Terms of Use and Privacy Policy.

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