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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 | |||
| LEVOMETHADYL ACETATE DISCONTINUED
| LEVOMETHADYL ACETATE | NERVOUS SYSTEM | ORAL | VD 1300 LITER (65 KILOGRAM) Cl 14.3 LITER / HOUR (65 KILOGRAM) HT 62 HOUR SOLUBILITY > 15 MILLIGRAM / MILLILITER | MU-TYPE OPIOID RECEPTOR | MU OPIOID RECEPTOR AGONIST CHEMBL233 MU OPIOID RECEPTOR P35372 MU-TYPE OPIOID RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE OPIOID RECEPTOR | EMA | |||
