• Molecular NameArformoterol
  • Synonym(R,R)-formoterol; arformoterol
  • Weight344.411
  • Drugbank_IDDB01274
  • ACS_NO67346-49-0
  • Show 3D model
  • LogP (experiment)N/A
  • LogP (predicted, AB/LogP v2.0)1.32
  • pkaN/A
  • LogD (pH=7, predicted)-0.53
  • Solubility (experiment)N/A
  • LogS (predicted, ACD/Labs)(ph=7)-1.25
  • LogSw (predicted, AB/LogsW2.0)12.75
  • Sw (mg/ml) (predicted, ACD/Labs)0.54
  • No.of HBond Donors4
  • No.of HBond Acceptors6
  • No.of Rotatable Bonds8
  • TPSA90.82
  • StatusFDA approved
  • Administrationnebuliser
  • PharmacologyA long acting beta-adrenoceptor agonist drug indicated for the treatment of chronic obstructive pulmonary disease (COPD).
  • Absorption_valueN/A
  • Absorption (description)N/A
  • Caco_2N/A
  • BioavailabilityN/A
  • Protein binding58.5
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmArformoterol was almost entirely metabolized following oral administration of 35 mcg of radiolabeled arformoterol in eight healthy subjects. Direct conjugation of arformoterol with glucuronic acid was the major metabolic pathway. O-Desmethylation is a secondary route catalyzed by the CYP enzymes CYP2D6 and CYP2C19.
  • Half life26 h
  • ExcretionN/A
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityA death was reported in dogs after a single oral dose of 5 mg/kg (approximately 4500 times the maximum recommended daily inhalation dose in adults on a mg/m2 basis). As with all inhaled sympathomimetic medications, cardiac arrest and even death may be associated with an overdose.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A