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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 | |||
| DIFLUNISAL
| DIFLUNISAL | NERVOUS SYSTEM | ORAL | Cmax 496 MICROMOLAR Tmax 2.5 HOUR VD 6.3 LITER (65 KILOGRAM) PPB 99 PERCENT Cl 0.39 LITER / HOUR (65 KILOGRAM) HT 10 HOUR SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | PROSTAGLANDIN G/H SYNTHASE 1 PROSTAGLANDIN G/H SYNTHASE 2 PDB 4I89 (CRYSTAL STRUCTURE OF TRANSTHYRETIN IN COMPLEX WITH DIFLUNISAL AT ACIDIC PH) LIGAND CODE = 1FL (link to the list of PDB complexes) Download experimental 3D coordinates of 1FL with added hydrogens | CYCLOOXYGENASE INHIBITOR CHEMBL2094253 CYCLOOXYGENASE P23219 PROSTAGLANDIN G/H SYNTHASE 1 HOMO SAPIENS ENZYME REDUCTASE | EMA | |||
