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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 | |||
| MELOXICAM
| MELOXICAM | MUSCULO-SKELETAL SYSTEM | ORAL INTRAVENOUS PERIARTICULAR | Cmax 3 MICROMOLAR Tmax 4.5 HOUR F 89 PERCENT VD 14.7 LITER PPB 99.4 PERCENT Cl 0.52 LITER / HOUR HT 20.1 HOUR SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | PROSTAGLANDIN G/H SYNTHASE | CYCLOOXYGENASE-2 INHIBITOR CHEMBL230 CYCLOOXYGENASE-2 P35354 PROSTAGLANDIN G/H SYNTHASE 2 HOMO SAPIENS ENZYME REDUCTASE | EMA | |||
