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  2. μ-opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Μ-opioid_receptor

    They are also referred to as μ(mu)-opioid peptide (MOP) receptors. The prototypical μ-opioid receptor agonist is morphine, the primary psychoactive alkaloid in opium and for which the receptor was named, with mu being the first letter of Morpheus, the compound's namesake in the original Greek.

  3. Opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Opioid_receptor

    An animated view of the human κ-opioid receptor in complex with the antagonist JDTic. Opioid receptors are a group of inhibitory G protein-coupled receptors with opioids as ligands. [1] [2] [3] The endogenous opioids are dynorphins, enkephalins, endorphins, endomorphins and nociceptin. The opioid receptors are ~40% identical to somatostatin ...

  4. Morphine - Wikipedia

    en.wikipedia.org/wiki/Morphine

    Morphine is a phenanthrene opioid receptor agonist – its main effect is binding to and activating the μ-opioid receptor (MOR) in the central nervous system. Its intrinsic activity at the MOR is heavily dependent on the assay and tissue being tested; in some situations it is a full agonist while in others it can be a partial agonist or even ...

  5. 6-Monoacetylmorphine - Wikipedia

    en.wikipedia.org/wiki/6-monoacetylmorphine

    It has also relatively weak affinity to μ-opioid receptors because the 3-hydroxy group, essential for effective binding to the receptor, is masked by the acetyl group. Therefore, heroin acts as a pro-drug, serving as a lipophilic transporter for the systemic delivery of morphine, which actively binds with μ-opioid receptors. [1] [2] Black tar ...

  6. Category:Mu-opioid receptor agonists - Wikipedia

    en.wikipedia.org/wiki/Category:Mu-opioid...

    Pages in category "Mu-opioid receptor agonists" The following 200 pages are in this category, out of approximately 291 total. This list may not reflect recent changes .

  7. Opioid-induced hyperalgesia - Wikipedia

    en.wikipedia.org/wiki/Opioid-induced_hyperalgesia

    The mu opioid receptor is targeted most often by opioids to relieve pain. [14] Two of the most commonly used opioid antagonists at the mu receptor are naltrexone and naloxone . [ 15 ] The pharmacology for opioid-induced hyperalgesia is more complicated, and is believed to involve the activation of NMDA receptors and increased excitatory peptide ...

  8. MS1 (drug) - Wikipedia

    en.wikipedia.org/wiki/MS1_(drug)

    [3] [4] MS1 shows potentiated analgesic effects with opioids in animals. [2] [3] [5] It also did not worsen opioid withdrawal symptoms, respiratory depression, or analgesic tolerance. [2] [3] [5] MS1 and other atypical MOR activators are of potential interest in the development of novel opioid analgesics with reduced adverse effects and misuse ...

  9. Opioid peptide - Wikipedia

    en.wikipedia.org/wiki/Opioid_peptide

    Opioid peptides or opiate peptides are peptides that bind to opioid receptors in the brain; opiates and opioids mimic the effect of these peptides. Such peptides may be produced by the body itself, for example endorphins .