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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 | |||
| PROPOXYPHENE DISCONTINUED (has an active metabolite)
| PROPOXYPHENE |
NERVOUS SYSTEM | ORAL | Cmax 0.21 MICROMOLAR (65 MILLIGRAM) Tmax 2.25 HOUR VD 780 LITER (65 KILOGRAM) PPB 80 PERCENT Cl 58.5 LITER / HOUR (65 KILOGRAM) HT 9 HOUR SOLUBILITY FREELY SOLUBLE IN WATER | OPIOID RECEPTOR | Mu-type opioid receptor UNIPROT P35372 OPRM1 more at DrugCentral | EMA | |||
