| | ||||||||||
| 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 | |||
| TROSPIUM
| TROSPIUM | METABOLISM | ORAL | Cmax 8.9 NANOMOLAR Tmax 5.5 HOUR F 9.6 PERCENT VD 395 LITER PPB 67 PERCENT Cl 13.6 LITER / HOUR (EQN) HT 20 HOUR SOLUBILITY 1 GRAM / 2 MILLILITER | MUSCARINIC ACETYLCHOLINE RECEPTOR M1 | MUSCARINIC ACETYLCHOLINE RECEPTOR M2 ANTAGONIST CHEMBL211 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 P08172 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ACETYLCHOLINE RECEPTOR | EMA | |||
