Duloxetine

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In vitro binding studies using synaptosomal preparations isolated from rat cerebral cortex indicated that duloxetine was approximately 3 fold more potent at inhibiting serotonin uptake than norepinephrine uptake.<ref name="a64">PMID:28913467</ref>
In vitro binding studies using synaptosomal preparations isolated from rat cerebral cortex indicated that duloxetine was approximately 3 fold more potent at inhibiting serotonin uptake than norepinephrine uptake.<ref name="a64">PMID:28913467</ref>
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<scene name='97/975936/Cv/2'>Sodium-dependent dopamine transporter in S-duloxetine bound form</scene> ([[6m38]]).
</StructureSection>
</StructureSection>
== References ==
== References ==
<references/>
<references/>

Revision as of 12:15, 12 July 2023

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References

  1. Stahl S (2013). Stahl's Essential Pharmacology (4th ed.). New York: Cambridge University Press. pp. 305, 308, 309.
  2. Stahl SM, Grady MM, Moret C, Briley M. SNRIs: their pharmacology, clinical efficacy, and tolerability in comparison with other classes of antidepressants. CNS Spectr. 2005 Sep;10(9):732-47. PMID:16142213 doi:10.1017/s1092852900019726
  3. Bymaster FP, Lee TC, Knadler MP, Detke MJ, Iyengar S. The dual transporter inhibitor duloxetine: a review of its preclinical pharmacology, pharmacokinetic profile, and clinical results in depression. Curr Pharm Des. 2005;11(12):1475-93. PMID:15892657 doi:10.2174/1381612053764805
  4. Onuţu AH. Duloxetine, an antidepressant with analgesic properties Rom J Anaesth Intensive Care. 2015 Oct;22(2):123-128 PMID:28913467

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