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Opioids and opioid receptors (Chapter 13) - The Essence of Analgesia and Analgesics
Inclusion complex of Tramadol in β-cyclodextrin enhances fluorescence by preventing self-quenching | SpringerLink
Comprehensive molecular pharmacology screening reveals potential new receptor interactions for clinically relevant opioids | PLOS ONE
PDF) When the Safe Alternative Is Not That Safe: Tramadol Prescribing in Children
PDF) In Vitro and In Vivo Pharmaco-Toxicological Characterization of 1-Cyclohexyl-x-methoxybenzene Derivatives in Mice: Comparison with Tramadol and PCP
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I'll Be Back”: The Resurrection of Dezocine | ACS Medicinal Chemistry Letters
Molecules | Free Full-Text | A Novel Multi-Target Mu/Delta Opioid Receptor Agonist, HAGD, Produced Potent Peripheral Antinociception with Limited Side Effects in Mice and Minimal Impact on Human Sperm Motility In Vitro
Comprehensive molecular pharmacology screening reveals potential new receptor interactions for clinically relevant opioids | PLOS ONE
Tramadol or Tramadont - REBEL EM - Emergency Medicine Blog
IJMS | Free Full-Text | In Vitro and In Vivo Pharmaco-Toxicological Characterization of 1-Cyclohexyl-x-methoxybenzene Derivatives in Mice: Comparison with Tramadol and PCP
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Mechanisms of tramadol-related neurotoxicity in the rat: Does diazepam/ tramadol combination play a worsening role in overdose? - ScienceDirect
The effect of tramadol on sneeze‐induced urethral continence reflex through μ‐opioid receptors in the spinal cord in rats - Ashikari - 2018 - Neurourology and Urodynamics - Wiley Online Library
The effect of tramadol on sneeze‐induced urethral continence reflex through μ‐opioid receptors in the spinal cord in rats - Ashikari - 2018 - Neurourology and Urodynamics - Wiley Online Library
Molecules | Free Full-Text | A Novel Multi-Target Mu/Delta Opioid Receptor Agonist, HAGD, Produced Potent Peripheral Antinociception with Limited Side Effects in Mice and Minimal Impact on Human Sperm Motility In Vitro
Comprehensive molecular pharmacology screening reveals potential new receptor interactions for clinically relevant opioids | PLOS ONE