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Item No. 34691
![Deltorphin II (trifluoroacetate salt) (DADELT II, [D-Ala2]Deltorphin II, [D-Ala2, Glu4]Deltorphin II, Tyr-D-Ala-Phe-Glu-Val-Val-Gly-NH2)](https://cdn2.caymanchem.com/cdn/productImages/34691.png)
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Deltorphin II is a peptide agonist of δ2-opioid receptors.1,2 It is selective for δ-opioid receptors over μ- and κ-opioid receptors in radioligand bindings assays (Kis = 0.0033, >1, and >1 µM, respectively) and induces [35S]GTPγS binding in mouse brain membrane preparations (EC50 = 0.034 µM). Deltorphin II (0.12 mg/kg) decreases the infarction zone:risk zone ratio in a rat model of myocardial ischemia-reperfusion injury induced by coronary occlusion, an effect that can be reversed by the δ2-opioid receptor antagonist naltriben but not the δ1-opioid receptor antagonist BNTX.3 Intrathecal administration of deltorphin II (15 µg/animal) increases latency to withdraw in the paw pressure and tail-flick tests in rats.4
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1. Pharmacological characterization of the cloned κ-
2. The delta agonists DPDPE and deltorphin II recruit predominantly mu receptors to produce thermal analgesia: A parallel study of mu, delta and combinatorial opioid receptor knockout mice. Eur. J. Neurosci. 19(8), 2239-2248 (2004).
3. Opioid peptide deltorphin II simulates the cardioprotective effect of ischemic preconditioning: role of δ2-
4. Antinociceptive effects of isoleucine derivatives of deltorphin I and deltorphin II in rat spinal cord: A search for selectivity of delta receptor subtypes. Neuropeptides 32(6), 511-517 (1998).