Chemistry:Cyprodime
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Short description: Chemical compound
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Other names | Cyprodime |
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Formula | C22H29NO3 |
Molar mass | 355.478 g·mol−1 |
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Cyprodime is an opioid antagonist from the morphinan family of drugs.
Cyprodime is a selective opioid antagonist which blocks the μ-opioid receptor,[1] but without affecting the δ-opioid or κ-opioid receptors. This makes it useful for scientific research as it allows the μ-opioid receptor to be selectively deactivated so that the actions of the δ and κ receptors can be studied separately, in contrast to better known opioid antagonists such as naloxone which block all three opioid receptor subtypes.[2]
See also
- Tianeptine, an atypical, selective MOR full-agonist licensed for major depression since 1989.
- Samidorphan, an opioid antagonist preferring the MOR, which is under development for major depression.
References
- ↑ "Synthesis and biological evaluation of 14-alkoxymorphinans. 2. (-)-N-(cyclopropylmethyl)-4,14-dimethoxymorphinan-6-one, a selective mu opioid receptor antagonist". Journal of Medicinal Chemistry 32 (2): 418–21. February 1989. doi:10.1021/jm00122a021. PMID 2536439.
- ↑ "Mu-opioid receptor specific antagonist cyprodime: characterization by in vitro radioligand and [35S]GTPgammaS binding assays". European Journal of Pharmacology 383 (2): 209–14. October 1999. doi:10.1016/s0014-2999(99)00610-x. PMID 10585536.
Original source: https://en.wikipedia.org/wiki/Cyprodime.
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