Eticlopride (hydro<wbr/>chloride)

Eticlopride (hydrochloride)

CAT N°: 29112
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From 102.00 86.70

Eticlopride is a dopamine D2 and D3 receptor antagonist (Kis = 0.029 and 0.46 nM in MN9D mouse neuronal cells expressing rat D2 and human D3 receptors, respectively).{45603} It is selective for dopamine D2 and D3 receptors (IC50s = 1 and 113 nM, respectively) over dopamine D1, ?2-adrenergic, and ?-adrenergic, histamine H1, and muscarinic receptors (IC50s = 700->100,000 nM), as well as the serotonin (5-HT) receptor subtypes 5-HT1 and 5-HT2 (IC50s = 6,200 and 830, respectively), but does bind ?1-adrenergic receptors (?1-ARs; IC50 = 110 nM) in radioligand binding assays.{45604} Eticlopride (10 ?g/kg) inhibits stereotyped behavior in rats induced by 7-hydroxy-N,N-di-n-propyl-2-aminotetralin (7-OH-DPAT).{45605} It also inhibits ketamine- and cocaine-induced hypermotility in rats when administered at doses of 20 and 50 ?g/kg, respectively.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 3-chloro-5-ethyl-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-6-hydroxy-2-methoxy-benzamide, monohydrochloride
  • Correlated keywords
    • 84226-12-0 A38503 A-38503 FLB 131 FLB131 S D-2 3 ? H-1 5HT1 5HT 5HT2 ?1AR OHDPAT 7OHDPAT
  • Product Overview:
    Eticlopride is a dopamine D2 and D3 receptor antagonist (Kis = 0.029 and 0.46 nM in MN9D mouse neuronal cells expressing rat D2 and human D3 receptors, respectively).{45603} It is selective for dopamine D2 and D3 receptors (IC50s = 1 and 113 nM, respectively) over dopamine D1, ?2-adrenergic, and ?-adrenergic, histamine H1, and muscarinic receptors (IC50s = 700->100,000 nM), as well as the serotonin (5-HT) receptor subtypes 5-HT1 and 5-HT2 (IC50s = 6,200 and 830, respectively), but does bind ?1-adrenergic receptors (?1-ARs; IC50 = 110 nM) in radioligand binding assays.{45604} Eticlopride (10 ?g/kg) inhibits stereotyped behavior in rats induced by 7-hydroxy-N,N-di-n-propyl-2-aminotetralin (7-OH-DPAT).{45605} It also inhibits ketamine- and cocaine-induced hypermotility in rats when administered at doses of 20 and 50 ?g/kg, respectively.

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