Tasipimidine

Tasipimidine
Clinical data
Trade namesTessie
Other namesODM-105; ODM105; ORM-19695; ORM19695
Routes of
administration
Dogs: Oral
Humans: unspecified
Drug classα2A-Adrenergic receptor agonist; Anxiolytic; Sedative; Hypnotic
Identifiers
  • 2-(5-methoxy-3,4-dihydro-1H-isochromen-1-yl)-4,5-dihydro-1H-imidazole
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC13H16N2O2
Molar mass232.283 g·mol−1
3D model (JSmol)
  • COC1=CC=CC2=C1CCOC2C3=NCCN3
  • InChI=1S/C13H16N2O2/c1-16-11-4-2-3-10-9(11)5-8-17-12(10)13-14-6-7-15-13/h2-4,12H,5-8H2,1H3,(H,14,15)
  • Key:GHIKYGQWBRHEGU-UHFFFAOYSA-N

Tasipimidine (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name; developmental code names ODM-105 and ORM-19695), sold under the brand name Tessie, is an α2-adrenergic receptor agonist which is approved for the short-term treatment of fear and anxiety in dogs. It is also under development for the treatment of insomnia in humans. The drug is used as an oral solution in dogs, whereas its route of administration for humans is unspecified.

The drug acts as a potent and selective full agonist of the human α2A-adrenergic receptor. Conversely, it is a much weaker agonist of the rodent α2B-, α2C-, and α2D-adrenergic receptors. In addition, it shows only low affinity for α1-adrenergic receptors, where it appears to act as a partial agonist. Tasipimidine produces anxiolytic, sedative, hypolocomotor, hypotensive, and bradycardic effects in animals.

Tasipimidine is under development for use in humans by Orion Corporation. As of October 2024, it is in phase 2 clinical trials for this indication. The drug is or was also under development for the treatment of psychiatric disorders in humans, but no recent development for this indication has been reported. It has reached phase 1 trials for psychiatric disorders. Tasipimidine was approved for treatment of fear and anxiety in dogs in the European Union in 2021.