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  2. Total synthesis of morphine and related alkaloids - Wikipedia

    en.wikipedia.org/wiki/Total_synthesis_of...

    Morphine. Synthesis of morphine-like alkaloids in chemistry describes the total synthesis of the natural morphinan class of alkaloids that includes codeine, morphine, oripavine, and thebaine and the closely related semisynthetic analogs methorphan, buprenorphine, hydromorphone, hydrocodone, isocodeine, naltrexone, nalbuphine, oxymorphone, oxycodone, and naloxone.

  3. μ-opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Μ-opioid_receptor

    Activation of the μ-opioid receptor by an agonist such as morphine causes analgesia, sedation, slightly reduced blood pressure, itching, nausea, euphoria, decreased respiration, miosis (constricted pupils), and decreased bowel motility often leading to constipation. Some of these effects, such as analgesia, sedation, euphoria, itching and ...

  4. Endorphins - Wikipedia

    en.wikipedia.org/wiki/Endorphins

    Endorphins may contribute to the positive effect of exercise on anxiety and depression. [43] The same phenomenon may also play a role in exercise addiction . Regular intense exercise may cause the brain to downregulate the production of endorphins in periods of rest to maintain homeostasis , causing a person to exercise more intensely in order ...

  5. Opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Opioid_receptor

    Heterotrimeric G proteins act as ‘molecular switches’, which play a key role in signal transduction, because they relay information from activated receptors to appropriate effector proteins. All G protein α sub-units contain palmitate, which is a 16-carbon saturated fatty acid, that is attached near the N-terminus through a labile ...

  6. Morphinan - Wikipedia

    en.wikipedia.org/wiki/Morphinan

    Morphinan has a phenanthrene core structure with the A ring remaining aromatic and the B and C rings being saturated, and an additional nitrogen-containing, six-membered, saturated ring, the D ring, being attached to carbons 9 and 13 of the core, and with the nitrogen being at position 17 of the composite.

  7. Leu-enkephalin - Wikipedia

    en.wikipedia.org/wiki/Leu-enkephalin

    The tyrosine residue at position 1 is thought to be analogous to the 3-hydroxyl group on morphine. [4] Leu-enkephalin has agonistic actions at both the μ-and δ-opioid receptors, with significantly greater preference for the latter. It has little to no effect on the κ-opioid receptor. [5] [6]

  8. Neurotransmitter - Wikipedia

    en.wikipedia.org/wiki/Neurotransmitter

    An example of a receptor agonist is morphine, an opiate that mimics effects of the endogenous neurotransmitter β-endorphin to relieve pain. Other drugs interfere with the deactivation of a neurotransmitter after it has been released, thereby prolonging the action of a neurotransmitter.

  9. Endomorphin - Wikipedia

    en.wikipedia.org/wiki/Endomorphin

    In addition to endomorphins, morphine and morphine-like opiates target the μ-opioid receptor. Thus, endomorphins pose significant potential as analgesics and morphine substitutes. [ 4 ] In vitro assessment of endomorphins as analgesics reveals similar behavior to morphine and other opiates, where drug tolerance leads to dependence and addiction.