Naloxone hydrochloride, Opioid antagonist
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(6 Publications)
MW 363.8 Da, Purity >98%. Competitive opioid antagonist. Achieve your results faster with highly validated, pure and trusted compounds.
View Alternative Names
D-OR-1, Delta type opioid receptor DOR 1, Delta-type opioid receptor, K-OR-1, Kappa opioid receptor, Kappa-type opioid receptor, LMOR, M-OR-1, MOR, Mu opiate receptor, Mu opioid receptor, Mu-type opioid receptor, Nbor, OPRD 1, OPRD_HUMAN, OPRK 1, OPRK_HUMAN, OPRM1, OPRM_HUMAN, Opiate receptor kappa 1, Opioid receptor delta 1, Opioid receptor mu 1, Opioid receptor, kappa 1, Oprk2, R21, hMOP, mDOR
- Chemical Structure
Lab
Chemical Structure - Naloxone hydrochloride, Opioid antagonist (AB120074)
2D chemical structure image of ab120074, Naloxone hydrochloride, Opioid antagonist
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Supplementary information
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Biological function summary
Opioid receptors are integral to the modulation of pain and reward systems. They exist as monomers or dimers and can form higher-order complexes with each other or with other GPCRs to influence signal transduction pathways. When activated by their ligands they inhibit cyclic adenosine monophosphate (cAMP) production which reduces neuronal excitability. By interacting with ligand molecules like herkinorin dermorphin and Mu agonists these receptors contribute to the analgesic and euphoric effects typical of opioid ligands.
Pathways
Delta Kappa and Mu receptors play key roles in the endogenous opioid signaling pathways and the dopaminergic reward pathway. These pathways influence neurotransmitter release and neuronal activity often associated with the sensation of pain relief and reward. The dopaminergic pathway also involves proteins like the dopamine transporter protein which works alongside these opioid receptors to regulate dopamine levels in synaptic clefts. Opioid antagonists like naloxone interact with these pathways by blocking the opioid receptors to reverse opioid-induced effects.
Publications (6)
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Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 21:e00377 PubMed38777742
2024
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Science advances 9:eadf6521 PubMed37224253
2023
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European journal of oral sciences 127:408-416 PubMed31365768
2019
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eLife 8: PubMed31099753
2019
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eLife 7: PubMed29589831
2018
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Molecular pain 6:96 PubMed21172011
2010
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