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Β-Chlornaltrexamine
Chemical compound From Wikipedia, the free encyclopedia
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β-Chlornaltrexamine (β-CNA) is a non-selective irreversible antagonist of the μ-opioid receptor (MOR), the δ-opioid receptor (DOR), and the κ-opioid receptor (KOR), which forms a covalent bond to the binding sites of these receptors and has ultra-long-lasting opioid antagonist effects.[1] Although it is predominantly antagonistic, β-CNA also shows some irreversible mixed agonist–antagonist activity at the MOR and KOR and some associated analgesic effects.[2][3] Its alkylating group is a bis(chloroalkyl)amino-residue similar to that of the nitrogen mustards.[4][5][6][7]
The drug was first described by 1978.[8][9] It should not be confused with its epimer and related drug α-chlornaltrexamine (α-CNA), which is likewise predominantly an irreversible antagonist of the opioid receptors but also shows some irreversible mixed agonist–antagonist activity.[10]
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See also
- Naltrexamine, an opioid receptor antagonist and the parent compound
- β-Funaltrexamine, a related irreversible opioid receptor antagonist
- Naloxazone, an irreversible μ-opioid receptor antagonist
- Methocinnamox, an irreversible μ-opioid receptor antagonist
- Chloroxymorphamine, an irreversible opioid receptor agonist
- Oxymorphazone, an irreversible opioid receptor agonist
References
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