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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 | |||
| FLAVOXATE
| FLAVOXATE | GENITO | ORAL | Tmax 1.86 HOUR | PDB 7E4A (CRYSTAL STRUCTURE OF MIF BOUND TO COMPOUND 13) LIGAND CODE = HWL (link to the list of PDB complexes) Download experimental 3D coordinates of HWL with added hydrogens | Phosphodiesterase 4 UNIPROT P27815 PDE4A -- Phosphodiesterase 7 UNIPROT Q13946 PDE7A more at DrugCentral | EMA | |||
