How selective is escitalopram?

Escitalopram has been investigated in more than 140 different receptor and binding assays. Apart from its effect on the 5-HT transporter, it has no significant activity at any of the other receptors/binding sites that have been tested (ref.1). Among these are several that are of particular pharmacological interest:

  • histamine H1
  • 5-HT1A and 5-HT2C
  • muscarine cholinergic
  • dopamine D1 and D2
  • noradrenaline a1, a2, b
  • sigma1 and sigma2
  • benzodiazepine
  • opioid.


In practice: escitalopram is highly specific and selective, and this translates into an excellent tolerability profile.


References:

1. Sánchez et al, 2002

Last updated: 31.07.2008
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