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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 | |||
| TAPENTADOL
| TAPENTADOL | NERVOUS SYSTEM | ORAL | Tmax 1.25 HOUR F 32 PERCENT VD 540 LITER PPB 20 PERCENT Cl 91.8 LITER / HOUR HT 4 HOUR SOLUBILITY LOGP = 2.87 | MU OPIOID RECEPTOR | Mu-type opioid receptor UNIPROT P35372 OPRM1 -- Sodium-dependent noradrenaline transporter UNIPROT P23975 SLC6A2 more at DrugCentral | EMA | |||
