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| 1 | INN | Class | Route (list) | PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693) | Primary Target and PDB code of Protein-Drug complex | Targets from DrugCentral | Links | |||
| FORMOTEROL
| FORMOTEROL |
RESPIRATORY SYSTEM | INHALATION | Cmax 0.26 NANOMOLAR Tmax 0.08 HOUR F 61 PERCENT VD 260 LITER (65 KILOGRAM) PPB 62.5 PERCENT Cl 84 LITER / HOUR HT 13 HOUR SOLUBILITY SLIGHTLY SOLUBLE IN WATER | BETA-2 ADRENERGIC RECEPTOR PDB 6H7K (ACTIVATED TURKEY BETA1 ADRENOCEPTOR WITH BOUND AGONIST FORMOTEROL) LIGAND CODE = FVN (link to the list of PDB complexes) Download experimental 3D coordinates of FVN with added hydrogens | BETA-2 ADRENERGIC RECEPTOR AGONIST CHEMBL210 BETA-2 ADRENERGIC RECEPTOR P07550 BETA-2 ADRENERGIC RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ADRENERGIC RECEPTOR | EMA | |||
