Naloxone benzoylhydrazone (NalBzoH) is a mixed agonist/antagonist. Naloxone benzoylhydrazone is a prototypicκ3-opioid receptoragonist, and a partial agonist at the clonedμandδ opioid receptors, and an antagonist atopioid-like NOP receptors. Naloxone benzoylhydrazone has potently analgesia effect^[1][2][3].

κ3-opioid receptor; μ- and δ-opioid receptors; Opioid-like NOP receptors^[1][2]

At the mu-opioid receptor (MOR), Naloxone benzoylhydrazone stimulates [³⁵S]GTPγS binding (pEC₅₀=8.59) and inhibits cyclic AMP accumulation (pEC₅₀=8.74) with maximal effects (E_max) corresponding to 55 and 65% of those obtained with the MOR agonist DAMGO, respectively^[1].
At the κ-opioid receptor (KOR), Naloxone benzoylhydrazone stimulates [³⁵S]GTPγS binding (pEC₅₀=9.70) and inhibits cyclic AMP formation (pEC₅₀=9.45)^[1].
In CHO cells expressing the δ-opioid receptor (DOR), Naloxone benzoylhydrazone increases [³⁵S]GTPγS binding (pEC₅₀=8.49) and inhibits cyclic AMP formation (pE₅₀=8.61)^[1].

Analgesic studies in mice examining increasing doses of Naloxone benzoylhydrazone with a fixed dose of morphine reveals a biphasic curve. Naloxone benzoylhydrazone at doses as low as 1 μg/kg partially antagonized morphine analgesia. Higher Naloxone benzoylhydrazone doses continued to inhibit morphine analgesia in a dose-dependent manner, with the 1-mg/kg dose antagonizing completely morphine analgesia. As the Naloxone benzoylhydrazone dose increased beyond 1 mg/kg analgesia returned. Naloxone benzoylhydrazone also prduces a similar analgesic response when administered alone in mice and also is active in rats. Naloxone benzoylhydrazone has excellent p.o. activity, with an analgesic potency in mice equivalent to s.c. administration. In addition to blocking morphine analgesia, low doses of Naloxone benzoylhydrazone also partially reverses the inhibition of gastrointestinal transit in mice produced by morphine, antagonizes completely morphine lethality and precipitates withdrawal in morphine-dependent mice^[4].

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C₂₆H₂₇N₃O₄

119630-94-3

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