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  2. Nociceptin receptor - Wikipedia

    en.wikipedia.org/wiki/Nociceptin_receptor

    The nociceptin opioid peptide receptor (NOP), also known as the nociceptin/orphanin FQ (N/OFQ) receptor or kappa-type 3 opioid receptor, is a protein that in humans is encoded by the OPRL1 (opioid receptor-like 1) gene. [5] The nociceptin receptor is a member of the opioid subfamily of G protein-coupled receptors whose natural ligand is the 17 ...

  3. Nociceptin - Wikipedia

    en.wikipedia.org/wiki/Nociceptin

    Nociceptin/orphanin FQ (N/OFQ), a 17-amino acid neuropeptide, is the endogenous ligand for the nociceptin receptor (NOP, ORL-1). Nociceptin acts as a potent anti-analgesic, effectively counteracting the effect of pain-relievers; its activation is associated with brain functions such as pain sensation and fear learning.

  4. Nociceptor - Wikipedia

    en.wikipedia.org/wiki/Nociceptor

    ' pain receptor ') is a sensory neuron that responds to damaging or potentially damaging stimuli by sending "possible threat" signals [1] [2] [3] to the spinal cord and the brain. The brain creates the sensation of pain to direct attention to the body part, so the threat can be mitigated; this process is called nociception .

  5. Opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Opioid_receptor

    This receptor is known as the nociceptin receptor or ORL1 (opiate receptor-like 1). The opioid receptor types are nearly 70% identical, with the differences located at the N and C termini. The μ receptor is perhaps the most important. It is thought that the G protein binds to the third intracellular loop of all opioid receptors.

  6. J-113,397 - Wikipedia

    en.wikipedia.org/wiki/J-113,397

    J-113,397 is an opioid drug which was the first compound found to be a highly selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor. [1] [2] It is several hundred times selective for the ORL-1 receptor over other opioid receptors, [3] [4] and its effects in animals include preventing the development of tolerance to morphine, [5] the prevention of hyperalgesia ...

  7. R6890 - Wikipedia

    en.wikipedia.org/wiki/R6890

    The pharmacology of R6890 is described as a nociceptin receptor (NOP) agonist, although R6890 retains significant activity at the mu opioid receptor. [5] R6890 has affinities (K i values) of 4, 75, and 10 nM for the mu, delta, and the total opioid receptor population, respectively.

  8. Ro65-6570 - Wikipedia

    en.wikipedia.org/wiki/Ro65-6570

    Ro65-6570 is an opioid drug, it works by activating opioid receptors. However, instead of acting at the mu , kappa and delta receptors, it is instead an agonist at the nociceptin receptor . [ 4 ]

  9. Ro64-6198 - Wikipedia

    en.wikipedia.org/wiki/Ro64-6198

    Ro64-6198 is an opioid drug used in scientific research. It acts as a potent and selective agonist for the nociceptin receptor, also known as the ORL-1 (opiate receptor like-1) receptor, with over 100x selectivity over the other opioid receptors. [1]

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